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	<title>discover Archives - MyMedicPlus</title>
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		<title>Scientists discover possible genetic target for treating endometriosis</title>
		<link>https://www.mymedicplus.com/blog/scientists-discover-possible-genetic-target-for-treating-endometriosis/</link>
		
		<dc:creator><![CDATA[mymedicplus]]></dc:creator>
		<pubDate>Fri, 13 Nov 2020 05:01:26 +0000</pubDate>
				<category><![CDATA[Uncategorized]]></category>
		<category><![CDATA[discover]]></category>
		<category><![CDATA[Endometriosis]]></category>
		<category><![CDATA[genetic]]></category>
		<category><![CDATA[Possible]]></category>
		<category><![CDATA[scientists]]></category>
		<category><![CDATA[Target]]></category>
		<category><![CDATA[Treating]]></category>
		<guid isPermaLink="false">http://www.mymedicplus.com/news/?p=6287</guid>

					<description><![CDATA[<p>The post <a href="https://www.mymedicplus.com/blog/scientists-discover-possible-genetic-target-for-treating-endometriosis/">Scientists discover possible genetic target for treating endometriosis</a> appeared first on <a href="https://www.mymedicplus.com/blog">MyMedicPlus</a>.</p>
]]></description>
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<p>Source &#8211; https://www.sciencedaily.com/</p>
<p id="first" class="lead">Michigan State University researchers have identified a potential genetic target for treating an especially painful and invasive form of endometriosis.</p>
<div id="text">
<p>Their study published in <em>Cell Reports</em>, a scientific journal, could lead to better treatments for women suffering from severe forms of endometriosis, said Mike Wilson, a postdoctoral fellow in the MSU College of Human Medicine. Wilson and Jake Reske, a graduate student in the MSU Genetics and Genome Sciences Program, are first authors of the study.</p>
<p>Their research focused on a type of endometriosis that occurs in women who have a mutation in a gene called ARID1A, which is linked to the more invasive and painful form of the disease. When ARID1A is mutated, so-called &#8220;super-enhancers,&#8221; a part of the DNA that determines the function of cells, run wild, Reske said. This allows the cells that normally line the uterus to form deep implants outside the uterus and cause severe pelvic pain.</p>
<p>&#8220;There haven&#8217;t been many successful nonhormonal therapies for this form of endometriosis that have made it to the bedside yet,&#8221; Reske said.</p>
<p>In laboratory experiments, he and Wilson tested a drug that appeared to target the super-enhancers and stop the spread of endometriosis. Such a drug &#8212; part of a new type of treatment called &#8220;epigenetic therapy&#8221; that controls how genes are expressed &#8212; could be far more effective than current treatments, including surgery, hormone therapy and pain management.</p>
<p>Endometriosis, particularly the kind associated with the ARID1A mutation, can be debilitating for many women, often leading to infertility.</p>
<p>&#8220;It can seriously impact women&#8217;s quality of life and their ability to have a family and work,&#8221; said Ronald Chandler, an assistant professor of obstetrics, gynecology and reproductive biology, who supervised the study. &#8220;It&#8217;s not easy to treat, and it can become resistant to hormone therapy. The most clinically impactful thing we found is that targeting super-enhancers might be a new treatment for this deeply invasive form of the disease.&#8221;</p>
<p>The drug they studied targeted a protein in cells called P300, suppressing the super-enhancers and offsetting the effects of the ARID1A mutation, Wilson said. The same type of treatment could be used to treat other forms on endometriosis, he said.</p>
<p>The researchers already are planning follow-up studies to find other drugs that could target P300, Wilson and Reske said.</p>
<p>The MSU team collaborated with Van Andel Institute researchers, providing them with tissue samples for VAI scientists to analyze with a machine called a next-generation sequencer.</p>
</div>
<p>The post <a href="https://www.mymedicplus.com/blog/scientists-discover-possible-genetic-target-for-treating-endometriosis/">Scientists discover possible genetic target for treating endometriosis</a> appeared first on <a href="https://www.mymedicplus.com/blog">MyMedicPlus</a>.</p>
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		<title>Scientists discover potential off-switch for type-2 diabetes</title>
		<link>https://www.mymedicplus.com/blog/scientists-discover-potential-off-switch-for-type-2-diabetes/</link>
		
		<dc:creator><![CDATA[mymedicplus]]></dc:creator>
		<pubDate>Thu, 06 Feb 2020 07:33:02 +0000</pubDate>
				<category><![CDATA[Diabetes]]></category>
		<category><![CDATA[discover]]></category>
		<category><![CDATA[potential]]></category>
		<category><![CDATA[scientists]]></category>
		<category><![CDATA[type-2 diabetes]]></category>
		<guid isPermaLink="false">http://www.mymedicplus.com/news/?p=4460</guid>

					<description><![CDATA[<p>The post <a href="https://www.mymedicplus.com/blog/scientists-discover-potential-off-switch-for-type-2-diabetes/">Scientists discover potential off-switch for type-2 diabetes</a> appeared first on <a href="https://www.mymedicplus.com/blog">MyMedicPlus</a>.</p>
]]></description>
										<content:encoded><![CDATA[
<p>SOurce: newatlas.com</p>
<p>Scientists at Yale University investigating the mechanisms at play in type-2 diabetes have discovered a new way they may be able to apply the brakes to the condition. The breakthrough centers on a new understanding of how fasting can drive the onset of type-2 diabetes, which led the researchers to unearth a way of intervening and switching the process off.</p>
<p>The research is described in a pair of studies published by Yale medical scientists, with the first focusing on a newly discovered connection between the body’s behavior when it is in a state of fasting, as it is while we sleep, and the development of type-2 diabetes.</p>
<p>The team found that fasting switches on a process whereby two proteins, TET3 and HNF4a, build up in the liver and elevate the production of blood glucose. In a healthy person, this process is switched off when the body exits fasting mode, but in those with type-2 diabetes that off-switch fails, leaving a surplus of glucose to build up in the blood.</p>
<p>By coming up with another way to switch it off, the scientists suspected they might be able to stop the disease from developing. In experiments designed to explore this theory, the team packaged genetic material called small interfering RNAs (siRNAs) inside viruses that target TET3 or HNF4 and injected it into mice. They found that this technique was effective at knocking down the levels of the proteins, along with blood glucose levels, “effectively stopping diabetes in its tracks.”</p>
<p>In the second study, the team explored the role TET3 plays in liver fibrosis, which is a scarring of healthy liver tissue that can lead to life-threatening conditions like cirrhosis. They found that TET3 plays a role at three different points along the fibrosis signaling pathway, meaning that drugs that can target these key proteins in type-2 diabetes could also be leveraged to treat fibrosis, for which there are currently very limited options.</p>
<p>“Right now, there are no effective drugs for the treatment of fibrosis,” says Xuchen Zhang, M.D., associate professor in pathology and co-author on the fibrosis study.</p>
<p>The post <a href="https://www.mymedicplus.com/blog/scientists-discover-potential-off-switch-for-type-2-diabetes/">Scientists discover potential off-switch for type-2 diabetes</a> appeared first on <a href="https://www.mymedicplus.com/blog">MyMedicPlus</a>.</p>
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