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<title>Medical Xpress: PHYSorg news tagged with: genetic alterations</title>
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<description>Medical Xpress internet news portal provides the latest news on Health and Medicine.</description>

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     <title>Many solid tumors carry genetic changes targeted by existing compounds</title>
   	 <description>Nearly two-thirds of solid tumors carry at least one mutation that may be targeted, or medicated, by an existing compound, according to new findings from researchers Fox Chase Cancer Center that will be presented at the 49th Annual Meeting of the American Society of Clinical Oncology on June 3. The results suggest that it may one day become commonplace for doctors to sequence tumors before deciding on a treatment regimen.</description>
	  <link>http://medicalxpress.com/news/2013-05-solid-tumors-genetic-compounds.html</link>
	 <category>Cancer</category>
	 <pubDate>Fri, 31 May 2013 11:34:20 EST</pubDate>
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     <title>Gene sequencing project finds new mutations to blame for a majority of brain tumor subtype</title>
   	 <description>(Medical Xpress)—The St. Jude Children's Research Hospital – Washington University Pediatric Cancer Genome Project has identified mutations responsible for more than half of a subtype of childhood brain tumor that takes a high toll on patients. Researchers also found evidence the tumors are susceptible to drugs already in development.</description>
	  <link>http://medicalxpress.com/news/2013-05-gene-sequencing-mutations-blame-majority.html</link>
	 <category>Genetics</category>
	 <pubDate>Thu, 30 May 2013 06:37:07 EST</pubDate>
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     <title>Three mutations at BRCA1 gene responsible for breast and ovarian hereditary cancer</title>
   	 <description>Researchers of the hereditary cancer research group at the Bellvitge Biomedical Research Institute (IDIBELL) and the Catalan Institute of Oncology (ICO) conducted a functional and structural study of seven missense variants of the BRCA1 gene concluding that three of these variants are pathogenic, linked to the risk of suffering breast or ovarian cancer. The study has been published in the journal PLoS One</description>
	  <link>http://medicalxpress.com/news/2013-04-mutations-brca1-gene-responsible-breast.html</link>
	 <category>Cancer</category>
	 <pubDate>Thu, 18 Apr 2013 13:11:46 EST</pubDate>
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     <title>Whole genome sequencing finds new mutations to blame for a majority of brain tumor subtype</title>
   	 <description>Washington University Pediatric Cancer Genome Project has identified mutations responsible for more than half of a subtype of childhood brain tumor that takes a high toll on patients. Researchers also found evidence the tumors are susceptible to drugs already in development.</description>
	  <link>http://medicalxpress.com/news/2013-04-genome-sequencing-mutations-blame-majority.html</link>
	 <category>Genetics</category>
	 <pubDate>Sun, 14 Apr 2013 13:00:13 EST</pubDate>
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     <title>The relationship between prenatal stress and obesity is confirmed in rats</title>
   	 <description>The intrauterine environment plays an important role in the health of the offspring. Now, experts from the University of Navarra affirm that the mother's stress, due to socio-economic or psycho-social causes, is associated with the development of pathologies related with obesity.</description>
	  <link>http://medicalxpress.com/news/2013-04-relationship-prenatal-stress-obesity-rats.html</link>
	 <category>Health</category>
	 <pubDate>Tue, 09 Apr 2013 12:01:35 EST</pubDate>
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     <title>KDM1 may represent a new therapeutic target for glioma</title>
   	 <description>Researchers have generated preclinical data demonstrating that the protein KDM1, which functions as a lysine demethylase, is a potential target for glioma treatment, according to Gangadhara R. Sareddy, Ph.D., a postdoctoral fellow in the Vadlamudi Laboratory at The University of Texas Health Science Center in San Antonio, who presented the results at the AACR Annual Meeting 2013, held in Washington, D.C., April 6-10.</description>
	  <link>http://medicalxpress.com/news/2013-04-kdm1-therapeutic-glioma.html</link>
	 <category>Cancer</category>
	 <pubDate>Mon, 08 Apr 2013 09:00:01 EST</pubDate>
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     <title>Comprehensive genomic analysis identifies alterations in head and neck cancer that could lead to targeted therapy</title>
   	 <description>Not all head and neck squamous cell carcinomas (HNSCCs) have the same pattern of genomic alterations, but those cancers with certain distinctive patterns could be amenable to specific targeted therapies, according to a researcher who presented the data at the AACR Annual Meeting 2013, held in Washington, D.C., April 6-10.</description>
	  <link>http://medicalxpress.com/news/2013-04-comprehensive-genomic-analysis-neck-cancer.html</link>
	 <category>Cancer</category>
	 <pubDate>Mon, 08 Apr 2013 08:31:52 EST</pubDate>
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     <title>Unique study reveals genetic 'spelling mistakes' that increase the risk of common cancers</title>
   	 <description>More than 80 genetic 'spelling mistakes' that can increase the risk of breast, prostate and ovarian cancer have been found in a large, international research study within the framework of the EU Network COGS. For the first time, the researchers also have a relatively clear picture of the total number of genetic alterations that can be linked to these cancers. Ultimately the researchers hope to be able to calculate the individual risk of cancer, to better understand how these cancers develop and to be able to generate new treatments.</description>
	  <link>http://medicalxpress.com/news/2013-03-unique-reveals-genetic-common-cancers.html</link>
	 <category>Cancer</category>
	 <pubDate>Wed, 27 Mar 2013 12:07:33 EST</pubDate>
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     <title>Colon cancer exhibits a corresponding epigenetic pattern in mice and humans</title>
   	 <description>Tumourigenesis is driven by genetic alterations and by changes in the epigenome, for instance by the addition of methyl groups to cytosine bases in the DNA. A deeper understanding of the interaction between the genetic and epigenetic mechanisms is critical for the selection of tumour biomarkers and for the future development of therapies. Human tumour specimens and cell lines however contain a plethora of genetic and epigenetic changes, which complicate data analysis. In contrast, certain mouse tumour models contain only a single genetic mutation and allow the analysis of nascent tumours. Scientists of the Max Planck Institute for Molecular Genetics in Berlin have now discovered a recurring pattern of more than 13,000 epigenetic alterations in young tumours of the mouse. This genome-wide pattern was found to be partly conserved in human colon carcinoma, and may therefor facilitate the identification of novel clinical colon cancer biomarkers for early detection.</description>
	  <link>http://medicalxpress.com/news/2013-02-colon-cancer-epigenetic-pattern-mice.html</link>
	 <category>Genetics</category>
	 <pubDate>Thu, 07 Feb 2013 17:00:03 EST</pubDate>
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     <title>Common genetic alteration found in head and neck cancers may not be key to effective treatment</title>
   	 <description>Although a large majority of head and neck cancers have a deregulation of the PI3K/AKT/mTOR pathway, data recently published in Cancer Research, a journal of the American Association for Cancer Research, indicated that deregulation of this pathway does not necessarily signify that the tumor is dependent on it for survival and progression.</description>
	  <link>http://medicalxpress.com/news/2013-01-common-genetic-neck-cancers-key.html</link>
	 <category>Cancer</category>
	 <pubDate>Tue, 29 Jan 2013 13:00:01 EST</pubDate>
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     <title>Study finds new genetic defects in high-risk childhood leukemia subtypes with chromosomal loss</title>
   	 <description>Research led by St. Jude Children's Research Hospital scientists has identified a possible lead in treatment of two childhood leukemia subtypes known for their dramatic loss of chromosomes and poor treatment outcomes.</description>
	  <link>http://medicalxpress.com/news/2013-01-genetic-basis-high-risk-childhood-cancer.html</link>
	 <category>Genetics</category>
	 <pubDate>Sun, 20 Jan 2013 13:00:01 EST</pubDate>
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     <title>Ability to metabolize tamoxifen affects breast cancer outcomes, study confirms</title>
   	 <description>For nearly a decade, breast cancer researchers studying the hormone therapy tamoxifen have been divided as to whether genetic differences in a liver enzyme affect the drug's effectiveness and the likelihood breast cancer will recur. A new study by researchers from the Mayo Clinic Cancer Center and the Austrian Breast and Colorectal Cancer Study Group provides evidence that genetic differences in the enzyme CYP2D6 play a key role in how well tamoxifen works.</description>
	  <link>http://medicalxpress.com/news/2012-12-ability-metabolize-tamoxifen-affects-breast.html</link>
	 <category>Cancer</category>
	 <pubDate>Thu, 27 Dec 2012 13:16:43 EST</pubDate>
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     <title>Preventing prostate cancer through androgen deprivation may have harmful effects</title>
   	 <description>Mice deficient in PTEN in the prostate developed stable precancers. Androgen deprivation promoted progression to invasive prostate cancer. Patients with PTEN-deficient prostate precancers may not benefit from androgen deprivation chemoprevention therapy.</description>
	  <link>http://medicalxpress.com/news/2012-12-prostate-cancer-androgen-deprivation-effects.html</link>
	 <category>Cancer</category>
	 <pubDate>Thu, 20 Dec 2012 10:39:48 EST</pubDate>
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     <title>Study unmasks regulator of healthy life span</title>
   	 <description>A new series of studies in mouse models by Mayo Clinic researchers uncovered that the aging process is characterized by high rates of whole-chromosome losses and gains in various organs, including heart, muscle, kidney and eye, and demonstrate that reducing these rates slows age-related tissue deterioration and promotes a healthier life span. The findings appear in today's online issue of Nature Cell Biology.</description>
	  <link>http://medicalxpress.com/news/2012-12-unmasks-healthy-life-span.html</link>
	 <category>Medical research</category>
	 <pubDate>Mon, 17 Dec 2012 12:38:32 EST</pubDate>
	 <guid isPermaLink="false">news274970304</guid>
	 
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     <title>Two new genetic mutations associated with Cowden syndrome</title>
   	 <description>Cleveland Clinic researchers from the Lerner Research Institute have uncovered two new genes associated with Cowden syndrome (CS) according to a new study, published today in the online version of the American Journal of Human Genetics.</description>
	  <link>http://medicalxpress.com/news/2012-12-genetic-mutations-cowden-syndrome.html</link>
	 <category>Genetics</category>
	 <pubDate>Thu, 13 Dec 2012 12:00:13 EST</pubDate>
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     <title>Diverse genetic alterations found in triple-negative breast cancers after neoadjuvant chemotherapy</title>
   	 <description>Many different genetic alterations were detected in tumor cells left behind after patients with triple-negative breast cancer were treated with chemotherapy prior to surgery (neoadjuvant chemotherapy), according to data presented at the 2012 CTRC-AACR San Antonio Breast Cancer Symposium. The investigators hope this knowledge will help move toward early personalized treatment to combat this aggressive subtype of breast cancer.</description>
	  <link>http://medicalxpress.com/news/2012-12-diverse-genetic-triple-negative-breast-cancers.html</link>
	 <category>Cancer</category>
	 <pubDate>Fri, 07 Dec 2012 10:20:23 EST</pubDate>
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     <title>Neuroblastoma patients with ARID1A and ARID1B mutations have more aggressive disease</title>
   	 <description>In a genome sequencing study of 74 neuroblastoma tumors in children, scientists at the Johns Hopkins Kimmel Cancer Center and the Children's Hospital of Philadelphia (CHOP) found that patients with changes in two genes, ARID1A and ARID1B, survive only a quarter as long as patients without the changes. The discovery could eventually lead to early identification of patients with aggressive neuroblastomas who may need additional treatments.</description>
	  <link>http://medicalxpress.com/news/2012-12-neuroblastoma-patients-arid1a-arid1b-mutations.html</link>
	 <category>Genetics</category>
	 <pubDate>Sun, 02 Dec 2012 13:00:52 EST</pubDate>
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     <title>Kidney tumors have a mind of their own</title>
   	 <description>New research has found there are several different ways that kidney tumours can achieve the same result – namely, grow.</description>
	  <link>http://medicalxpress.com/news/2012-11-kidney-tumors-mind.html</link>
	 <category>Cancer</category>
	 <pubDate>Wed, 21 Nov 2012 09:39:27 EST</pubDate>
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     <title>Identification of mutations common to half of all liver cancers provides leads for new therapeutics</title>
   	 <description>Liver cancer is the sixth most common cancer worldwide and the third leading cause of cancer-associated deaths. Yet even for such a frequent and deadly disease, the pathogenesis of this cancer remains obscure. Now, a team of scientists in Japan has shown that genes involved in regulating how tightly DNA is wound into chromosomes are commonly mutated in liver tumors. The finding points to potential new and much-needed therapeutic strategies.</description>
	  <link>http://medicalxpress.com/news/2012-11-identification-mutations-common-liver-cancers.html</link>
	 <category>Cancer</category>
	 <pubDate>Fri, 16 Nov 2012 07:14:42 EST</pubDate>
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     <title>Genome sequencing of Burkitt Lymphoma reveals unique mutation</title>
   	 <description>In the first broad genetic landscape mapped of a Burkitt lymphoma tumor, scientists at Duke Medicine and their collaborators identified 70 mutations, including several that had not previously been associated with cancer and a new one that was unique to the disease.</description>
	  <link>http://medicalxpress.com/news/2012-11-genome-sequencing-burkitt-lymphoma-reveals.html</link>
	 <category>Genetics</category>
	 <pubDate>Mon, 12 Nov 2012 11:03:27 EST</pubDate>
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     <title>Biomarkers of behavior, therapeutic targets for adult B-acute lymphoblastic leukemia identified</title>
   	 <description>New insight into the aggressive behavior of certain adult B-acute lymphoblastic leukemias has provided researchers with a potential new prognostic biomarker and a promising new therapeutic target.</description>
	  <link>http://medicalxpress.com/news/2012-10-biomarkers-behavior-therapeutic-adult-b-acute.html</link>
	 <category>Cancer</category>
	 <pubDate>Mon, 29 Oct 2012 11:10:01 EST</pubDate>
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     <title>Researchers identify novel genes that may drive rare, aggressive form of uterine cancer</title>
   	 <description>Researchers have identified several genes that are linked to one of the most lethal forms of uterine cancer, serous endometrial cancer. The researchers describe how three of the genes found in the study are frequently altered in the disease, suggesting that the genes drive the development of tumors. The findings appear in the Oct. 28, 2012, advance online issue of Nature Genetics. The team was led by researchers from the National Human Genome Research Institute (NHGRI), part of the National Institutes of Health.</description>
	  <link>http://medicalxpress.com/news/2012-10-genes-rare-aggressive-uterine-cancer.html</link>
	 <category>Cancer</category>
	 <pubDate>Sun, 28 Oct 2012 14:10:06 EST</pubDate>
	 <guid isPermaLink="false">news270630547</guid>
	 <media:thumbnail url="http://s.ph-cdn.com/newman/gfx/news/tmb/2012/nihresearche.jpg" width="90" height="90" />
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     <title>First large scale trial of whole-genome cancer testing for clinical decision-making reported</title>
   	 <description>For the first time, researchers have conducted a large trial in which they tested the entire genome of individual breast cancers to help personalize treatment. They released their findings at the ESMO 2012 Congress of the European Society for Medical Oncology in Vienna.</description>
	  <link>http://medicalxpress.com/news/2012-10-large-scale-trial-whole-genome-cancer.html</link>
	 <category>Cancer</category>
	 <pubDate>Mon, 01 Oct 2012 03:31:45 EST</pubDate>
	 <guid isPermaLink="false">news268281097</guid>
	 
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     <title>Stemming the spread of cancer</title>
   	 <description>Okayama University's Masaharu Seno and colleagues have demonstrated in vitro the development of cancer stem cells (CSCs) from a type of normal stem cell exposed to their hypothetical microenvironment of a tumor. </description>
	  <link>http://medicalxpress.com/news/2012-09-stemming-cancer.html</link>
	 <category>Cancer</category>
	 <pubDate>Fri, 21 Sep 2012 06:49:26 EST</pubDate>
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	 <media:thumbnail url="http://s.ph-cdn.com/newman/gfx/news/tmb/2012/stemmingthes.jpg" width="90" height="90" />
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     <title>Team creates a unique mouse model for the study of aplastic anaemia</title>
   	 <description>Aplastic anaemia is characterised by a reduction in the number of the bone marrow cells that go on to form the different cell types present in blood (essentially red blood cells, white blood cells and platelets). In most cases, the causes of the disorder are hard to determine, but some patients have been found to have genetic alterations leading to a shortening of their telomeres (the end regions of chromosomes that protect and stabilise DNA).</description>
	  <link>http://medicalxpress.com/news/2012-08-team-unique-mouse-aplastic-anaemia.html</link>
	 <category>Medical research</category>
	 <pubDate>Wed, 29 Aug 2012 10:55:55 EST</pubDate>
	 <guid isPermaLink="false">news265456549</guid>
	 
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     <title>Blood test could guide treatment for kidney cancer</title>
   	 <description>A common enzyme that is easily detected in blood may predict how well patients with advanced kidney cancer will respond to a specific treatment, according to doctors at Duke Cancer Institute.</description>
	  <link>http://medicalxpress.com/news/2012-08-blood-treatment-kidney-cancer.html</link>
	 <category>Cancer</category>
	 <pubDate>Mon, 13 Aug 2012 16:00:08 EST</pubDate>
	 <guid isPermaLink="false">news264091838</guid>
	 
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     <title>Existing drugs offer new treatment options for high-risk childhood leukemia subtype</title>
   	 <description>Scientists have identified new genetic alterations underlying a high-risk subtype of the most common childhood cancer that could be effectively targeted with existing leukemia therapies.</description>
	  <link>http://medicalxpress.com/news/2012-08-drugs-treatment-options-high-risk-childhood.html</link>
	 <category>Cancer</category>
	 <pubDate>Mon, 13 Aug 2012 12:52:00 EST</pubDate>
	 <guid isPermaLink="false">news264081090</guid>
	 
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     <title>Researchers create powerful new method to analyze genetic data</title>
   	 <description>University of Texas Medical Branch at Galveston researchers have developed a powerful visual analytical approach to explore genetic data, enabling scientists to identify novel patterns of information that could be crucial to human health.</description>
	  <link>http://medicalxpress.com/news/2012-06-powerful-method-genetic.html</link>
	 <category>Genetics</category>
	 <pubDate>Tue, 12 Jun 2012 12:19:36 EST</pubDate>
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     <title>Distinct molecular subtype of prostate cancer identified</title>
   	 <description>A collaborative expedition into the deep genetics of prostate cancer has uncovered a distinct subtype of the disease, one that appears to account for up to 15 percent of all cases, say researchers at Weill Cornell Medical College, the Broad Institute of MIT and Harvard and the Dana-Farber Cancer Institute.</description>
	  <link>http://medicalxpress.com/news/2012-05-distinct-molecular-subtype-prostate-cancer.html</link>
	 <category>Genetics</category>
	 <pubDate>Sun, 20 May 2012 13:00:16 EST</pubDate>
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     <title>Molecular subtypes and genetic alterations may determine response to lung cancer therapy</title>
   	 <description>Cancer therapies targeting specific molecular subtypes of the disease allow physicians to tailor treatment to a patient's individual molecular profile. But scientists are finding that in many types of cancer the molecular subtypes are more varied than previously thought and contain further genetic alterations that can affect a patient's response to therapy.</description>
	  <link>http://medicalxpress.com/news/2012-05-molecular-subtypes-genetic-response-lung.html</link>
	 <category>Cancer</category>
	 <pubDate>Fri, 11 May 2012 15:12:55 EST</pubDate>
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