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	<title>Sam Min, Author at The McGill Daily</title>
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		<title>Uncovering the functions of circular RNAs</title>
		<link>https://www.mcgilldaily.com/2017/09/uncovering-the-functions-of-circular-rnas/</link>
		
		<dc:creator><![CDATA[Sam Min]]></dc:creator>
		<pubDate>Mon, 18 Sep 2017 10:30:52 +0000</pubDate>
				<category><![CDATA[Sci + Tech]]></category>
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					<description><![CDATA[<p>Circular RNAs may serve as a marker for cancers</p>
<p>The post <a href="https://www.mcgilldaily.com/2017/09/uncovering-the-functions-of-circular-rnas/">Uncovering the functions of circular RNAs</a> appeared first on <a href="https://www.mcgilldaily.com">The McGill Daily</a>.</p>
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										<content:encoded><![CDATA[<p><span style="font-weight: 400;">The central dogma in molecular biology is that the genetic information of an organism is encoded in the DNA molecules, which serve as a template for the synthesis of RNA molecules. RNA will in turn serve as a template for the manufacturing of proteins. Standard textbooks say proteins are only produced from the mRNA, a type of RNA molecule that has a linear shape. However, it has been recently found that proteins could be produced from another kind of RNA with a circular shape, the circRNAs. </span></p>
<p><span style="font-weight: 400;">A recent </span><a href="http://mobile.the-scientist.com/article/49873/uncovering-functions-of-circular-rnas"><span style="font-weight: 400;">study</span></a><span style="font-weight: 400;"> conducted by Sebastian Kadner and his colleagues found that in drosophilia (fruit flies), some proteins were made from circRNAs. This finding challenged the long-held belief that only linear RNAs were responsible for making proteins. Much of the literature in molecular biology focuses on linear RNAs because researchers thought circRNAs were a vestige from our evolution, which rendered them useless in manufacturing proteins.</span></p>
<p><span style="font-weight: 400;">Researchers </span><a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5440908/"><span style="font-weight: 400;">Shujuan Meng</span></a><span style="font-weight: 400;"> and colleagues have inferred possible associations between circRNA expression levels and the potential occurrence of cancers. miR-7 is a microRNA that stops cells from growing and dividing. CDR1as, one of the better characterized circRNAs, will produce proteins that disrupt the proper functioning of miR-7. So what would happen if one has a lot of CDR1as? Cells would then grow and divide uncontrollably – a phenomenon we usually see in metastasizing cancer cells and tumors.</span></p>
<p><span style="font-weight: 400;">Five years ago, we did not know much about circRNA because we thought it wouldn’t produce any proteins in mammals. Now we are aware that they may act as a marker for certain cancers.  </span></p>
<p>The post <a href="https://www.mcgilldaily.com/2017/09/uncovering-the-functions-of-circular-rnas/">Uncovering the functions of circular RNAs</a> appeared first on <a href="https://www.mcgilldaily.com">The McGill Daily</a>.</p>
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		<title>Progress in cancer research</title>
		<link>https://www.mcgilldaily.com/2017/09/progress-in-cancer-research/</link>
		
		<dc:creator><![CDATA[Sam Min]]></dc:creator>
		<pubDate>Sun, 10 Sep 2017 23:43:52 +0000</pubDate>
				<category><![CDATA[Sci + Tech]]></category>
		<category><![CDATA[brain]]></category>
		<category><![CDATA[cancer]]></category>
		<category><![CDATA[chemotherapy]]></category>
		<category><![CDATA[healthcare]]></category>
		<category><![CDATA[mcgill daily sci+tech]]></category>
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					<description><![CDATA[<p>A perspective from the case of medulloblastoma</p>
<p>The post <a href="https://www.mcgilldaily.com/2017/09/progress-in-cancer-research/">Progress in cancer research</a> appeared first on <a href="https://www.mcgilldaily.com">The McGill Daily</a>.</p>
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										<content:encoded><![CDATA[<p>Cells in our body usually operate in an orderly fashion: they divide and undergo apoptosis as the body needs them. However, cancerous cells grow and divide uncontrollably; they don’t undergo their programmed deaths when they are damaged. Cancer often appears in the form of a mass of cancerous cells, known as a tumor. Some cancers are malignant, meaning they can break off from their source of origin and invade other healthy tissues, creating havoc and breaking things one by one. One month a patient might see a mass on their chest, the next the patient might have a hard time breathing. The cancer has spread from one place to another, and this is called metastasis. Cancers can start anywhere in the body: blood, bones, or internal organs.</p>
<p>The primary cancer treatments are chemotherapy, radiotherapy and surgery. However, depending on the type of cancer, one treatment may work and another may not. Through chemotherapy, an oncologist applies several drugs to reduce and remove a tumor. During radiotherapy a doctor beams radiation to trim down the tumor size. Chemotherapy and radiotherapy are employed first, followed by surgery. In surgery, a surgeon cuts a chunk of the targeted organ where the tumour lies.</p>
<blockquote><p>One month a patient might see a mass on their chest, the next the patient might have a hard time breathing.</p></blockquote>
<p>Medulloblastoma is a cancer that originates in the cerebellum, a part of the brain that coordinates movement and balance. 75% of the affected patients are under ten years old. Following primary cancer treatments, severe side-effects occur including neurocognitive deficits, endocrine problems, meningioma and sterility. Many healthy organs are subject to toxic damage from sessions of chemotherapy. This damage is even more severe in children because their cells divide more quickly, meaning the spread of toxins is faster. Surgery also carries high risks as the cerebellum is located just above the spinal cord.</p>
<p>To look for alternative treatments, a research group in Tennessee suggested a new strategy to treat medulloblastoma. The Tennessee group used a novel molecule named HHAntag691 that blocks a pathway named Sonic Hedgehog (SHH). When the SHH pathway is active, the cells in the cerebellum called granule cell precursors multiply uncontrollably, and medulloblastoma appears. Through the action of HHAntag691, the rampant proliferation stops.</p>
<blockquote><p>Many healthy organs are subject to toxic damage from sessions of chemotherapy.</p></blockquote>
<p>This method was later tested in clinical trials. In 2008, a patient was treated with a similar but not identical molecule to HHAntag691 during clinical trial phase I &#8211; this is the phase when scientists apply drugs of interest that they had used on animals to humans. Before the treatment, the cancer had already spread. After the treatment, the cancer disappeared completely in 2 months. Sadly, the patient died 3 months after the treatment when the tumor relapsed. This was because a mutation had occurred, altering the SHH pathway and rendering the drug ineffective. Although unfortunately the patient did not survive, this was the first successful case of targeted-therapy, where only one type of cancer is tackled.</p>
<p>Passing the four phases of a clinical trial is required to get a drug approved. Vismodegib, the commercial name of the drug that has completed the first case of targeted therapy, is at phase II. In 2015, the drug worked better in Medulloblastoma patients who had a mutated SHH pathway than the ones with no mutation in the SHH pathway.</p>
<p>Medulloblastoma shows how powerful a cancer can be. Scientists have painstakingly developed new strategies to provide target-specific treatments against cancer, but it only takes one mutation from a cancer cell for a patient to become drug-resistant. Perhaps one obvious reason that cancer is like a death sentence to us is that it morphs our fundamental biological processes to favor itself. So despite advancements, it seems cancer research still has a long way to go.</p>
<p>The post <a href="https://www.mcgilldaily.com/2017/09/progress-in-cancer-research/">Progress in cancer research</a> appeared first on <a href="https://www.mcgilldaily.com">The McGill Daily</a>.</p>
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