Page 1,480«..1020..1,4791,4801,4811,482..1,4901,500..»

Does genetics make me what I am? – Sunbury Daily Item

Posted: August 21, 2017 at 4:42 am

Two timely issues call into question our use of genetics, both in science and popular usage: CRISPR technology used in the pre-natal state to genetically edit-out/repair potentially fatal genes, and the Google controversy.

CRISPR Clustered Regularly Interspersed Short Palindromic Repeats technology, discovered by scientists at UC Berkeley and modified by those at MIT, will almost certainly result in a Nobel Prize. Berkeley scientists discovered that these repeats were used by bacteria to protect themselves against viral infections. Between the repeats, they found pieces of the viral DNA that had previously attacked the bacterium. If, and when, the same virus again attacked, the intruder viral DNA would be compared to the DNA stored between the repeats. If it is recognized as a repeat offender, the bacterium sends in proteins to destroy the viral DNA. They additionally noted that in non-virally infected bacteria, CRISPR could be used to delete some bacterial genes and replace them with others.

Our use of this technology in human cells allows injection of the DNA-modifying proteins into a human egg while it is being fertilized in a test-tube. Fatal genetic conditions identified in the mother or father in the recent report this was a cardiac abnormality, hypertrophic cardiomyopathy can potentially be corrected pre-natally and, after the correction, the fertilized egg implanted into the mother. An incredibly promising technology, it may allow, as with this cardiac abnormality, children at-risk for sudden death to grow old.

Of course, there are ethical concerns related to this technology. Will it be used to create perfect people, eliminating the diversity that makes us better and stronger? That is up to us. A head-in-the-sand refusal to engage with this is not the answer.

The scientific use of genetics and the concept of diversity, above, is tied to its non-scientific use in the Googles James Damore controversy.

Damore spent 3,400 words to say three things: Women and ethnic minorities are genetically different than (select) men; Those genetic differences are why there are more men than women (and minorities) in positions of power; Refusing to acknowledge this creates all sorts of difficulties and controversy, and is bad for business.

Google, he argues, doesnt allow ideas such as his from being discussed, as people are shamed into silence.

The differences between men and women in the workplace are due to inherent, genetic differences, he claims. What?

There are differences between men and women phenotypic (hair color, eye color) and genotypic (a slight variation in genes coding for gender) for which I am always pleased. Do these explain workplace differences? Pay differences? IQ? No. What we term Intelligence Quotient is heavily influenced by surroundings and upbringing, including social class. Not that inherent ability is meaningless, but environment matters. It is not nurture versus nature, it is nurture and nature.

There is a thoughtful part of Damores thesis, meriting consideration. Diversity is right because it makes us better and stronger; we should welcome diverse voices. He muddles this logical point by claiming women are paid less than men for the same job because they spend more money and, somehow, this is genetic; so much for diversity.

Genetics both does and does not make us who we are. Yes, there are genetic elements within us that make us phenotypically what we are: Brown eyes rather than green; black hair rather than blond. But brilliance? Thoughtfulness? Humanity? Empathy? The ability to work together to solve a problem? To work on a problem day after day until the solution appears?

If there is a genetics to this, it is the ability of multiple genes to be turned on by stimulation in a young person. These on-switches are flipped by parents and a society that loves and provides for the child, allows the child to explore and ask questions. A society that takes the child seriously. A society that does not think of the child, the sum of her phenotype, what she looks like.

The danger from CRISPR technology is it could be used to create the perfect human, eliminating the diversity that makes us better, and our world more beautiful. Damores paper, without using such technology, does just that. He turns women and ethnic minorities into caricatures of themselves, while asserting that it is he who is not appreciated or valued.

Peoples opinions vary, but facts suggest we are surrounded by conservative voices, of which I am a multi-faceted one.

CRISPR technology has downsides; we need international guardrails for its use. But the misuse of genetics to explain our societys flaws is an error of the highest magnitude. Much more dangerous than the CRISPR tool-set, we see it in action every day. In papers such as Mr. Damores, and in the way we think of, and treat, our children, boys and girls.

Our world view, ideology, is like the air we breathe: invisible, almost indescribable. It is this ideological view that allows Damore and sometimes us to simultaneously argue for diversity, while doing all in our power to eliminate it.

Follow Dr. A. Joseph Layon on Twitter @ajlayon or on his health blog, also titled Notes from the Southern Heartland (ajlayon.com). Letters may be sent to: LettersNFTSH@gmail.com.

Continue reading here:
Does genetics make me what I am? - Sunbury Daily Item

Posted in Genetics | Comments Off on Does genetics make me what I am? – Sunbury Daily Item

Mercia invests further in Oxford Genetics – Insider Media

Posted: August 21, 2017 at 4:42 am

Warwickshire-based investor Mercia Technologies has injected 2m into a business that produces virus and protein-based biologics for therapeutic companies.

The direct follow-on investment into Oxford Genetics brings Mercia's equity stake in the business to 40.5 per cent.

The 2m from Mercia formed part of a 7.5m funding round, which included Invesco Asset Management.

Proceeds will be used to bolster Oxford Genetics' operation in the US with the opening of a new office in Boston. The company will also expand its research and development facility in the UK.

Chief executive Ryan Cawood said: "The next few years for Oxford Genetics will be exciting. The industry for complex biologics has taken such huge steps forward to delivering real patient benefit and we are pleased to be providing our technology to many of the companies tackling some of medicine's most important unmet needs."

Mercia has worked with Oxford Genetics since 2012 and has ploughed a total of 4.7m into its development.

Mark Payton, chief executive of Mercia and board director of Oxford Genetics, added: "This sector is growing rapidly, driven by pharma and biotech companies' relentless drive for new therapeutics.

"The commercial validity of the business has been recently supported by a string of technology licence agreements. This syndicated investment alongside Invesco reflects our confidence in Oxford Genetics' strong position and its ability to deliver shareholder value in the medium term."

Read more here:
Mercia invests further in Oxford Genetics - Insider Media

Posted in Genetics | Comments Off on Mercia invests further in Oxford Genetics – Insider Media

Can genetics refute white supremacist theories? – BioEdge

Posted: August 21, 2017 at 4:42 am

This weeks headlines were filled with news from Charlottesville, Virginia, after a white supremacist drove his car into a crowd of people opposing a march of supremacists and noe-Nazis, killing one woman and injuring many others. Which leads one to ask: how white are American white supremacists?

For most of them, the most convincing way to prove their whiteness is DNA tests from companies like 23andMe.com and Ancestry.com. To their consternation, the results are often not what they expected. White supremacist Craig Cobb was outed on daytime TV in 2013 as 86 percent European, and 14 percent Sub-Saharan African.

Whats interesting is how the white supremacists respond to these disconcerting test results. Aaron Panofsky and Joan Donovan, sociologists at UCLA, studied online discussions of genetic ancestry test results on the white nationalist website Stormfront. They found that the participants used fairly sophisticated reasoning to challenge the results and regain their whiteness.

Cobb, for instance, denounced his test as statistical noise and described it as a Jewish conspiracy to spread junk science whose intent is to defame, confuse and deracinate young whites on a mass levelespecially males. Using a test from another company he was able to claim that he was European, apart from a 3% Iberian thing.

Panofsky and Donovan conclude that genetics cannot refute racist views. Even though mankind probably came from Africa and even though the notion of racial purity is absurd, racists can manipulate and interpret data for their own purposes. They conclude:

clear communication, simple forms of education, and collective denunciations of scientific misuses, scientists preferred forms of anti-racist action, are insufficient for the task. Challenging racists public understanding of science is not simply a matter of more education or nuance, but may require scientists to rethink their research paradigms and reflexively interrogate their own knowledge production.

More here:
Can genetics refute white supremacist theories? - BioEdge

Posted in Genetics | Comments Off on Can genetics refute white supremacist theories? – BioEdge

Evolutionary Biologists Probe Long-standing Genetics Mystery – Yale News

Posted: August 21, 2017 at 4:42 am

August 17, 2017

Photo credit: Dreamstime

What makes humans different from chimpanzees? Evolutionary biologists from Howard University and the Yale School of Public Health have developed a unique genetic analysis technique that may provide important answers.

Michael C. Campbell, Ph.D., the papers first author and assistant professor in the Howard University Department of Biology, and co-author Jeffrey Townsend, Ph.D., the Elihu Associate Professor in Biostatistics at Yale, published their findings in the journal Molecular Biology and Evolution.

Their methodModel Averaged Site Selection via Poisson Random Field (MASS-PRF)looks at protein-coding genes to identify genetic signatures of positive selection. These signatures are actually DNA changes that contribute to the development of beneficial traits, or human adaptations, that emerged during human evolutionary history and that are shared across the human species.

It's a quantum leap in our statistical power to detect selection in recently diverged species.

Other approaches have examined this question but analyses have focused on whole genes, typically missing focused evolution that often occurs in small regions of genes. The method Campbell and Townsend created identifies selection within genes, pinpointing sets of mutations that have undergone positive selection.

Our method is a new way of looking for beneficial mutations that have become fixed or occur at 100 percent frequency in the human species, Campbell said. What we are concerned with are mutations within genes and traits that are specific to humans compared to closely related species, such as the chimpanzee. Essentially, we want to know is what are the mutations and traits that make us human and that unite us as a biological species.

Townsend said the technique has far-reaching implications. It helped the research team discover several genes whose evolution appears to have been critical to the divergence of humans from their common ancestor with chimpanzees. The genes play roles in neurological processing, immunity, and reproduction, and the method could eventually help scientists identify many more. It's a quantum leap in our statistical power to detect selection in recently diverged species, Townsend said.

Campbell began the research project with Drs. Zhao and Townsend while they were associate research scientists in the Department of Biostatistics at the Yale School of Public Health, before he arrived at Howard University in 2015. Dr. Zhao, currently a research scientist at The Jackson Laboratory for Genomic Medicine, co-authored the paper.

This article was submitted by Elisabeth Ann Reitman on August 17, 2017.

Read the original:
Evolutionary Biologists Probe Long-standing Genetics Mystery - Yale News

Posted in Genetics | Comments Off on Evolutionary Biologists Probe Long-standing Genetics Mystery – Yale News

Increased Confidence Earns Myriad Genetics An Upgrade – Benzinga

Posted: August 21, 2017 at 4:42 am

Deutsche Bank upgraded Myriad Genetics, Inc. (NASDAQ: MYGN), as it believes the risk/reward is now balanced following the company below-consensus sales and earnings per share guidance for 2018.

The firm upgraded the rating from Sell to Hold, with the price target at $28.

At time of writing, shares of Myriad Genetics were rallying 3.19 percent to $28.75.

Analyst Dan Leonard said he was earlier concerned that the Street numbers were too high and didn't sufficiently reflect downside in the company's Hereditary Cancer Testing, or HTC, business, which accounts for 74 percent of the total sales. The company's sales guidance for 2018 was 4 percent below the Street estimates at the midpoint, the analyst noted.

See also: August PDUFA Dates: Biotech Investors Stay Tuned To A Month Of Plenty

Deutsche Bank believes the price erosion in the core hereditary cancer testing business is likely to be metered post 2019, given that cost of HCT isn't a large portion of spend at any given payer.

Additionally, the firm noted that payers have historically used prior authorization as the primary lever to limit genetic testing spend, rather than price. The firm said payers may not prefer discriminating between providers, given the challenge posed by getting acquainted with the evolving medical practice, the firm said.

Meanwhile, Deutsche Bank also indicated Myriad Genetics is able to convince payers that the other HCT options aren't perfect substitutes for its tests due to its variant database and the FDA approved status of its BRCAnalysis test.

The firm also sees opportunity for volume gains to continue.

Deutsche Bank believes the Street estimates through 2020 now appear more appropriate, while opining that its estimates are largely in line save some timing differences.

"We would be more constructive on greater conviction in MYGN's efforts outside of hereditary cancer testing and/or greater volume growth in hereditary cancer testing," the firm concluded.

View More Analyst Ratings for MYGN View the Latest Analyst Ratings

Posted-In: Deutsche Bank - Dan LeonardAnalyst Color Upgrades Analyst Ratings Best of Benzinga

2017 Benzinga.com. Benzinga does not provide investment advice. All rights reserved.

View post:
Increased Confidence Earns Myriad Genetics An Upgrade - Benzinga

Posted in Genetics | Comments Off on Increased Confidence Earns Myriad Genetics An Upgrade – Benzinga

When White Nationalists Get DNA Tests Revealing African Ancestry … – The Atlantic

Posted: August 21, 2017 at 4:42 am

The white-nationalist forum Stormfront hosts discussions on a wide range of topics, from politics to guns to The Lord of the Rings. And of particular and enduring interest: genetic ancestry tests. For white nationalists, DNA tests are a way to prove their racial purity. Of course, their results dont always come back that way. And how white nationalists try to explain away non-European ancestry is rather illuminating of their beliefs.

Will the Alt-Right Promote a New Kind of Racist Genetics?

Two years agobefore Donald Trump was elected president, before white nationalism had become central to the political conversationAaron Panofsky and Joan Donovan, sociologists then at the University of California, Los Angeles, set out to study Stormfront forum posts about genetic ancestry tests. They presented their study at the American Sociological Association meeting this Monday. (A preprint of the paper is now online.)After the events in Charlottesville this week, their research struck a particular chord with the audience.

For academics, there was some uneasiness around hearing that science is being used in this way and that some of the critiques that white nationalists are making of genetics are the same critiques social scientists make of genetics, says Donovan, who recently took up a position at the Data and Society Research Institute. On Stormfront, the researchers did encounter conspiracy theories and racist rants, but some white-nationalist interpretations of genetic ancestry tests were in fact quite sophisticatedand their views cannot all be easily dismissed as ignorance.

If we believe their politics comes from lack of sophistication because theyre unintelligent or uneducated, says Panofsky, I think were liable to make a lot of mistakes in how we cope with them.

Panofsky, Donovan, and their team of researchers analyzed 3,070 Stormfront posts spanning more than a decadeall from forum threads in which at least one user revealed the results of a DNA test. Some of the results were 100 percent European, as users expected. But oftensurprisingly often, says Panofskyusers disclosed tests results showing non-European ancestry. And despite revealing non-European ancestry on a forum full of white nationalists, they were not run off the site.

While some commenters reacted with anger, many reacted by offering up arguments to explain away the test results. These arguments largely fell into two camps.

First, they could simply reject all genetic ancestry testing. Genealogy or the so-called mirror test (When you look in the mirror, do you see a Jew? If not, youre good) were better tests of racial purity, some suggested. Others offered up conspiracies about DNA testing companies led by Jews: I think 23andMe might be a covert operation to get DNA the Jews could then use to create bio-weapons for use against us.

The second category of explanation was a lot more nuancedand echoed in many ways legitimate critiques of the tests. When companies like 23andMe or AncestryDNA return a result like 23 percent Iberian, for example, theyre noting similarities between the customers DNA and people currently living in that region. But people migrate; populations change. It doesnt pinpoint where ones ancestors actually lived. One Stormfront user wrote:

See, THIS is why I dont recommend these tests to people. Did they bother to tell you that there were whites in what is now Senegal all that time ago? No? So they led you to believe that youre mixed even though in all probability, you are simply related to some white fool who left some of his DNA with the locals in what is now Senegal.

Panofsky notes that legitimate scientific critiques are often distorted by a white-nationalist interpretation of history. For example, the mixing of DNA in a region would be explained by the heroic conquest of Vikings. Or a white female ancestor was raped by an African man.

The team also identified a third group of reactions: acceptance of the genetic ancestry test results. Some users did start to rethink white nationalism. Not the basic ideologyStormfronts forums are not exactly the place you would do thatbut the criteria for whiteness. For example, one user suggested a white-nationalist confederation, where different nations would have slightly different criteria for inclusion:

So in one nation having Ghengis Khan as your ancestor wont disqualify you, while in others it might. Hypothetically, I might take a DNA test and find that I dont qualify for every nation and every nations standards, though I'm sure that at least one of those nations (and probably many of them) will have standards that would include me

Another user dug deep into the technical details of genetic ancestry testing. The tests can rely on three different lines of evidence: the Y chromosome that comes from your fathers fathers father and so on, the mitochondrial DNA that comes from your mothers mothers mother and so on, and autosomal DNA that can come from either side. One user suggested that a purity in the Y chromosome and mitochondrial DNA were more important than in the autosomal DNA. But others disagreed.

Sociologists have long pointed out the categories of race are socially constructed. The criteria for who gets to be whiteItalians? Arabs? Mexicans?are determined by social rather than biological forces. And DNA is the newest way for white nationalists to look for differences between the races.

In these years of posts on Stormfront, you can see users attempting to make sense of DNA, figuring out in real time how genetics can be used to circumscribe and preserve whiteness. The test results are always open to interpretation.

Go here to see the original:
When White Nationalists Get DNA Tests Revealing African Ancestry ... - The Atlantic

Posted in Genetics | Comments Off on When White Nationalists Get DNA Tests Revealing African Ancestry … – The Atlantic

This Wasp’s Larvae Sometimes Grow Hundreds of Soldier ClonesBut Why? – Entomology Today

Posted: August 21, 2017 at 4:40 am

The parasitoid wasp Copidosoma floridanum has been closely studied by entomologists for its extreme proliferation at the embryonic stage, with as many as 3,000 larvae emerging from a single egg. Some of those larvae develop into soldiers, and a new study shows more will do so in response to competition from other parasitoids in the same host but not to environmental conditions such as heat shock or bacterial infection. (Photo credit: John Rosenfeld, Bugguide.net)

Imagine, for a moment, having 3,000 twin sisters. You all live inside a caterpillar, but its home, and your numbers serve as a veritable army against any trespassers.

Such is the life of the parasitoid wasp Copidosoma floridanum, one of the insect worlds most fascinating examples of polyembryony, in which multiple embryos form from a single egg. C. floridanum females lay eggs inside the eggs of certain moth species; when the moth larva hatches, the wasp egg gives rise to as many as 3,000 clone embryos.

But wait, theres more.

C. floridanum also exhibits polyphenism, in which different types of wasp larvae develop from the same genetic materialbest known for its role in the caste system (queen, worker, soldier, etc.) appearing in social insects such as ants and bees. C. floridanum produces two different types of larvae: reproducers and soldiers. The reproducers emerge during the moth larvas last instar, consume it, and pupate into adult wasps. The soldiers, however, emerge earlier but never molt, and they die when the host dies. Instead, they spend their time defending their reproductive siblings by attacking other parasitoids present in the same host larva. The script isnt always the same, though, as C. floridanum can shift the number of soldier larvae it produces, and it is also known that male eggs tend to produce fewer and less-aggressive soldier larvae.

Researchers, of course, want to know why all of this happens. In a study published in July in the Annals of the Entomological Society of America, a team led by Margaret Smith, Ph.D., assistant professor at the University of North Georgia (and previously a postdoctoral researcher at the University of Georgia, where a portion of the research was conducted), explore the conditions that spur increased soldier development in Copidosoma floridanum as well as some of the underlying biological mechanisms driving it. We decided to do both experiments in this paper because we knew part of the story but wanted to fill in a few important missing pieces, says Smith.

In a study on the parasitoid waspCopidosoma floridanum, the presence of competitor parasitoidMicroplitis demolitorresulted in a shift toward generating more soldier larvae in theC. floridanum brood, whileheat shock and bacterial infection had no influence. Future research may seek to understand the cellular basis forC. floridanums caste formation. (Photo credit: Scott Justis, Bugguide.net)

Previous research showed that the presence of competitors was linked with increased soldier production in C. floridanum. Smith and colleagues tested whether other external factors were also related. (Shifts in caste development in other insect groups are commonly exhibited as responses to environmental conditions.) They found, however, that heat shock and bacterial infection had no influence on soldier production. Only multiparasitism, in the form the presence of competitor parasitoid Microplitis demolitor, led to increased soldier production in their experiment.

What about M. demolitor causes C. floridanum to shift toward more soldier production? The researchers tested that, too, and found that the M. demolitor egg chorion is the trigger.

As C. floridanum embryos proliferate, the differentiator between reproductive and soldier larvae is the presence or absence of a primary germ cell during embryo division. Embryos without the primary germ cells become soldier larvae. Smith and colleagues found that, in response to multiparasitism, female broods of C. floridanum rapidly shift (within 16 hours) to produce more embryos without primary germ cells. The same shift did not occur, however, in male broods.ll of this adds up to a deeper understanding of how polyembryony and polyphenism have evolved in C. floridanum. I think that these findings are important because they advance our understanding of caste formation in this species, Smith says. C. floridanum is different than many social insects in that caste is determined by the presence of germline stem cells and not environmentally. Understanding this species more helps us better understand the variation in evolution of caste differentiation and plasticity in general.

Left unanswered, however, is exactly how C. floridanum engineers the caste shift, something Smith says he hopes to answer in the future.

Id really like to understand more about the cellular basis of caste formation, says Smith. Is gene expression altered so that primary germ cells adopt a non-germline fate? Do broods physically move the primary germ cell so that they fail to end up in daughter embryos during proliferation?

Like Loading...

Related

View original post here:
This Wasp's Larvae Sometimes Grow Hundreds of Soldier ClonesBut Why? - Entomology Today

Posted in Georgia Stem Cells | Comments Off on This Wasp’s Larvae Sometimes Grow Hundreds of Soldier ClonesBut Why? – Entomology Today

Epigenetics? – What is Epigenetics? – Epigenome NOE

Posted: August 19, 2017 at 5:42 pm

In brief

Epigenetics has always been all the weird and wonderful things that cant be explained by genetics.Denise Barlow (Vienna, Austria)

DNA is just a tape carrying information, and a tape is no good without a player. Epigenetics is about the tape player.Bryan Turner (Birmingham, UK)

I would take a picture of a computer and say that the hard disk is like DNA, and then the programmes are like the epigenome. You can access certain information from the hard disk using the programmes on the computer. But there are certain password protected areas and those which are open. I would say were trying to understand why there are passwords for certain regions and why other regions are open.Jrn Walter (Saarland, Germany)

There is around 2m of DNA in a nucleus of only a few micrometers. We are trying to learn about the mechanisms whereby the DNA gets accessed given the tiny volume of the nucleus.Gunter Reuter (Halle, Germany)

Information management in the nucleus means that some of the genetic information is very very tightly packaged in the genome. Then there is genetic information that has to be on and active all the time, house-keeping genes for example. So epigenetics is a bit like information management at home, something that you need all the time you will not store away, but your old school records you keep packed in boxes in the attic.Peter Becker (Munich, Germany)

The difference between genetics and epigenetics can probably be compared to the difference between writing and reading a book. Once a book is written, the text (the genes or DNA: stored information) will be the same in all the copies distributed to the interested audience. However, each individual reader of a given book may interpret the story slightly differently, with varying emotions and projections as they continue to unfold the chapters. In a very similar manner, epigenetics would allow different interpretations of a fixed template (the book or genetic code) and result in different read-outs, dependent upon the variable conditions under which this template is interrogated.Thomas Jenuwein (Vienna, Austria)

Read more here:
Epigenetics? - What is Epigenetics? - Epigenome NOE

Posted in Epigenetics | Comments Off on Epigenetics? – What is Epigenetics? – Epigenome NOE

‘Magical’ Mushroom Could Fight off Cancer with Epigenetics – WhatIsEpigenetics.com

Posted: August 19, 2017 at 5:42 pm

A certain type of mushroom might epigenetically prevent tumor growth, according to a study published in the Journal of Cancer Research and Treatment. A medicinal mushroom, Phellinus linteus (PL), could come with magical anticancer properties. Researchers from New York Medical College found that histone deacetylase (HDAC) inactivation and histone acetylation led to the death of bladder cancer cells.

Chemotherapy and immunotherapy often come with severe side effects, and for those suffering from bladder cancer, the use of these therapies is limited and often ineffective in the long run. Because of this, a group of scientists sought to find a possible alternative therapy, one that relies on extracts of a very special type of fungus.

According to the researchers, Phellinus linteus has been used in Asian countries for centuries to prevent or treat ailments, including gastroenteric dysfunction, diarrhea, hemorrhage, rheumatoid arthritis, and cancers. In the wild, this mushroom can be found growing on mulberry trees. Interestingly, it is consumed in the form of hot tea in Korean traditional medicine.

Previous articles on What is Epigenetics detail the epigenetic effects and potential cancer-fighting benefits of broccoli, fruits, and other plants. Research has even found that a natural compound in cypress trees could protect against cancer and that green tea might be able to turn genes on or off in women. However, we are still in the beginning stages of understanding and researching these effects and whether they translate to humans in a practical manner.

Now the focus is on mushrooms. The group of researchers aimed to measure the epigenetic effect of this well-known mushroom on the growth of urothelial cell carcinoma(UCC), the most common type of bladder cancer. Those suffering from this particular cancer have limited therapeutic options. Often, the tumor returns, and the side effects brought on by chemotherapy or immunotherapy are a significant drawback.

In one of the first studies assessing the potential benefits of mushrooms against bladder cancer, these researchers found that the growth of human cancer cells was reduced from 60 to 90 percent and that histone deacetylase activity was significantly lost. The results were obtained by examining the effects of three distinct PL extracts on UCC cells in vitro.

HDACs are epigenetic enzymes that remove chemical groups, known as acetyl groups, from histone proteins. DNA wraps around these histones and the expression of our genes is changed depending on how loose or tight the structure is. Read more about chromatin remodeling and the impact it has on gene expression.

Removing an acetyl group will allow the histones to wrap around the DNA more tightly, which will prevent the expression of certain genes. Often times, cancer cells are treated with HDAC inhibitors (HDACi) because HDACs can cause aberrant transcription of key genes that regulate cell functions often linked to cancer, such as cell proliferation, cell-cycle regulation, and apoptosis.

In this study, HDAC activity was reduced as a result of cancerous cells being treated with mushroom extracts and histone acetylation was increased. The researchers used the Epigenase HDAC Activity/Inhibition Direct Assay Kit from EpiGentek to measure HDAC activity. They found that greater than 60% of HDAC activity was reduced after treatment with three distinct extracts or fractions of the mushroom (PL-I, -II, and -III). In addition, both histones H3 and H4 were highly acetylated, which indicated alterations in the chromatin structure.

The present study shows that all three PL-fractions, PL-I, -II, and -III, have anticancer effects on [bladder cancer] cells, although PL-III appears to be the most potent, reported the researchers. Such an anticancer mechanism is attributed to a p21-mediated cell cycle arrest with epigenetic modifications involving HDAC inactivation and hyperacetylation of H3 and H4, ultimately leading to apoptotic cell death.

Overall, the mushroom extracts reduced cell viability through anticancer activity, and histone modifications were thought to induce cell cycle arrest. In light of these results, this mushroom could modify the chromatin structure consisting of histones and DNA ultimately reducing cancer cell viability via a cell cycle arrest. The researchers suggest that DNA methylation, another popular epigenetic mechanism, should be investigated in terms of possible epigenetic effects of these fungus fractions.

This study raises new questions about whether nontraditional medicines could help those suffering from cancer. As we continue to conduct more research and investigate the epigenetic effects of various natural substances on human health and well being, we can begin to understand the potential benefits of alternative medicine and consider developing new therapies in the future.

Source: Bhalodi, A. et al. (2016). Alternative Therapeutic Approach to Urothelial Cell Carcinoma with Medicinal Mushroom Extracts. Journal of Cancer Research and Treatment, 4(5): 73-79.

See original here:
'Magical' Mushroom Could Fight off Cancer with Epigenetics - WhatIsEpigenetics.com

Posted in Epigenetics | Comments Off on ‘Magical’ Mushroom Could Fight off Cancer with Epigenetics – WhatIsEpigenetics.com

More Than Just Genes: How Environment, Lifestyle, and Stress Impact ADHD – ADDitude

Posted: August 19, 2017 at 5:42 pm

Our understanding of ADHD has grown by leaps and bounds over the past 30 years. What started as hyperkinetic impulse disorder its primary symptom excessive hyperactivity over time shifted to attention deficit disorder and a focus on problems with inattention, then to reward functioning, and later to executive functioning. None of these translations was wrong, in and of itself;each set of highlighted symptoms is a distinct and important part of the disorder we now call ADHD. But the facets were poorly integrated with one another, and thus painted an incomplete picture of a highly complex condition.

Now, researchers understand that ADHD is primarily a disorder of self-regulation. Self-regulation weaves together all the older theories of ADHD into one cohesive picture; it is also what allows humans to manage impulses, engage or disengage attention, and navigate between deliberate and automatic responses to different situations. The ability to self-regulate is managed across the brain in highly interconnected ways; similar brain nodes regulate both attention and emotion and when one area isnt performing well, the others suffer, too.

The newest theories of ADHD, then, dont focus on a single underperforming area of the brain, as older ones did. Its now understood that ADHD manifests when neurons misfire in the ever-shifting communications and connections between multiple areas of the brain. Emerging research also suggests that these neurological wrinkles may be driven by the environment as much (or more) than they are by genes.

[Quiz: Can You Tell the Difference Between ADHD Myths and ADHD Facts?]

This new framework provides a much more nuanced and complex view of ADHD, but it also provides hope: If ADHD symptoms can be worsened by environmental causes, they can be improved by them, too. Read on to find out how.

Researchers have long known that ADHD can be passed down genetically. But the idea that we can find the single gene responsible for ADHD and fix it is now understood to be outdated. The newest theory of ADHD, as a disorder primarily related to self-regulation, relies on something called epigenetics.

Epigenetics refers to biological traits or changes that cannot be explained by a persons genetic code. Epigenetic mechanisms actually create a physical mark on the DNA when a person undergoes an important experience, whether its positive or negative. These marks which can be added methyl molecules, or a modified histone tail adjust the individuals gene function, changing what the genes do or how strongly they express themselves. In a nutshell, environment and experiences affect a humans development and behavior in an enduring fashion actually altering regions of DNA, with effects that may last for an entire lifetime.

How does it work? It starts with genes the building blocks of who we are and who we become. But beginning at conception, everyone is exposed to different environmental toxins and advantages and after were born, psychological inputs like stress, adversity, and even trauma begin to factor in. Epigenetics takes this input and uses it to change how genes are expressed meaning a genes output isnt fully known until environment and personal history are factored in.

[Free Resource: What to Eat (and Avoid) for Improved ADHD Symptoms]

Epigenetics paints a much more complicated view of ADHD, but also a much more optimistic one; genes do not solely determine an individuals fate. In fact, while genes may make someone more prone to certain diseases or disorders, including ADHD, the entire genetic system is highly dynamic and responsive to input. This means its possible to change the expression of a persons ADHD genes by making certain environmental changes.

Credible and robust epigenetics research confirms these assertions. One experiment1 took two genetically identical mice embryo and, during the prenatal stage, fed their mothers diets that included the toxic element bisphenol-A (BPA). The diet of one mouses mother, however, was supplemented with nutrients like choline, folic acid, and B12; that mouse was later able to avoid the negative effects of the BPA, including obesity and a higher risk of cancer. This phenomenon can be explained by epigenetics the additional nutrients were able to turn off the genes that respond to BPA, and thus protect the mouse from its harmful effects.

Another experiment2 this one involving humans tested whether taking an omega-3 supplement during pregnancy would impact the attention abilities of a mothers child. The study found that children whose mothers had randomly received the supplement had stronger attention at 6 and 12 months, and later had better-developed mental abilities, than did children whose mothers had not taken the supplement. Since this experiment was randomized and the effect was so great, researchers were able to determine a causal effect and again, one that was influenced by epigenetics. Food dyes, artificial preservatives, and lead yielded similar results3 the introduction of each into a childs pre- or post-natal environment had real, causal effects on his or her attention, hyperactivity, and emotional regulation.

Similar experiments have been done on stress and adversity and how exercise can counteract those negative effects. One experiment4 placed rats into a stressful situation for a period of time each day, which resulted in significant epigenetic changes that decreased healthy function. However, when those same rats were also allowed to exercise while still experiencing the stressor the negative effects on the brain were completely eliminated. The study provided a clear example of how exercise can reverse the harmful brain-based effects of a negative early-life experience.

[Daily Exercise Ideas to Boost Focus]

This research suggests that lifestyle changes may help to offset the effects of ADHD genes activated by genetic, chemical, dietary, or other factors. More epigenetic research is needed, however a few things are clear: Omega-3 supplementation, aerobic exercise, and stress management can have real, positive effects on ADHD symptoms in both children and adults.

How big are these effects? Some changes, like reducing the amount of TV a child watches each day, have very small effects on ADHD symptoms only slightly noticeable in a familys everyday life. Others, like increasing omega-3 intake or introducing an exercise regimen, have significantly larger effect sizes up to twice or three times as large as reducing screen time.

Researchers now recommend that anyone with ADHD follows these strategies:

Continuing research is creating an ever-growing body of evidence regarding which lifestyle changes improve ADHD symptoms, and which are less useful. Though findings are still preliminary, the evidence is already strong enough to make them actionable. Simple changes, like exercising more or taking a fish oil supplement, can have real, lasting effects on an individuals ADHD symptoms in other words, genes do not seal your fate.

Learn more in Dr. Niggs book, Getting Ahead of ADHD: What Next-Generation Science Says about Treatments That Work and How You Can Make Them Work for Your Child

1Dolinoy DC, Huang D, Jirtle RL. Maternal Nutrient Supplementation Counteracts Bisphenol A-Induced DNA Hypomethylation in Early Development. PNAS, vol. 104, 2007, pp. 1305613061.2Colombo, John, et al. Maternal DHA and the Development of Attention in Infancy and Toddlerhood. Child Development, vol. 75, no. 4, 2004, pp. 12541267., doi:10.1111/j.1467-8624.2004.00737.x.3 Stevenson, J, et al. The Role of Histamine Degradation Gene Polymorphisms in Moderating the Effects of Food Additives on Childrens ADHD Symptoms. The American Journal of Psychiatry, vol. 167, no. 9, Sept. 2010, pp. 11081115.4 Kashimoto, R.K., et al. Physical Exercise Affects the Epigenetic Programming of Rat Brain and Modulates the Adaptive Response Evoked by Repeated Restraint Stress. Behavioural Brain Research, vol. 296, 2016, pp. 286289., doi:10.1016/j.bbr.2015.08.038.

Read more here:
More Than Just Genes: How Environment, Lifestyle, and Stress Impact ADHD - ADDitude

Posted in Epigenetics | Comments Off on More Than Just Genes: How Environment, Lifestyle, and Stress Impact ADHD – ADDitude

Page 1,480«..1020..1,4791,4801,4811,482..1,4901,500..»