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Survival of the fittest: even cancer cells follow the laws of evolution
August 04, 2008
New article in the FASEB Journal reveals that each type of cancer contains unique gene mutations that give it Darwin's 'selective advantage' Scientists from The Institute of Advanced Studies at Princeton and the University of California discovered that the underlying process in tumor formation is the same as for life itself-evolution. After analyzing a half million gene mutations, the researchers found that although different gene mutations control different cancer pathways, each pathway was controlled by only one set of gene mutations. This suggests that a molecular "survival of the fittest" scenario plays out in every living creature as gene mutations strive for ultimate survival through cancerous tumors. This finding, which appears in the August 2008 issue of The FASEB Journal ( http://www.fasebj.org), improves our understanding of how evolution shapes life in all forms, while laying a foundation for new cancer drugs and treatments. "This study lays the groundwork for understanding the nature of different mutations in cancers," said Chen-Hsiang Yeung, first author of the study, "and helps with understanding the mechanisms of cancers and their responses to drug treatments." To arrive at these conclusions, researchers analyzed about 500,000 cancer mutation records from the Catalog of Somatic Mutations in Cancer database and then divided the data into 45 tissue types. Within each tissue type, they calculated the frequency that multiple genes were mutated in the same sample. They identified the frequencies of mutations that were significantly higher or lower than if the genes had mutated independently. Then they mapped out how these genes ultimately lead to cancerous tumors and checked whether the genes occurring in specific tissues used the same or different cancer pathways. "Little could Darwin have known that his 'Origin of the Species' would one day explain the 'Origin of the Tumor,'" said Gerald Weissmann, MD, Editor-in-Chief of The FASEB Journal. "This research report completely changes our understanding of the many gene mutations that cause cancer." Federation of American Societies for Experimental Biology
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MRI best for carriers of BRCA gene mutations: study shows MRI detects more breast cancers in this population than do ultrasound or ... An article from: Family Practice News
by Betsy Bates (Author)
This digital document is an article from Family Practice News, published by International Medical News Group on December 1, 2004. The length of the article is 979 words. The page length shown above is based on a typical 300-word page. The article is delivered in HTML format and is available in your Amazon.com Digital Locker immediately after purchase. You can view it with any web browser.
Citation Details Title: MRI best for carriers of BRCA gene mutations: study shows MRI detects more breast cancers in this population than do ultrasound or mammography.(Women's Health)(Magnetic resonance imaging) Author: Betsy Bates Publication: Family Practice News (Magazine/Journal) Date: December 1, 2004 Publisher: International Medical News Group Volume: 34 Issue: 23 Page:...
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Pneumocystis jiroveci Dihydropteroate Synthase Gene Mutations Among Colonized Individuals and Pneumocystis Pneumonia Patients From Spain (Postgraduate Medicine)
by JTE Multimedia
Cotrimoxazole, an association of trimethoprim and sulfamethoxazole, and dapsone, are mainstays for the prophylaxis and treatment of Pneumocystis pneumonia (PcP). The inability to culture Pneumocystis prevents routine susceptibility testing and detection of drug resistance. Instead, molecular techniques have been used to detect Pneumocystis jiroveci dihydropteroate synthase (DHPS) mutations that cause sulfa resistance in other microorganisms. The most frequent DHPS mutations occur at nucleotide positions 165 and 171, which lead to an amino acid change at positions 55 and 57. Several studies suggest that these mutations are associated with the failure of chemoprophylaxis for PcP. The aim was to establish the frequency and characteristics of P jiroveci DHPS mutations among colonized...
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Genetic Bypass: Using Nutrition To Bypass Genetic Mutations
by Dr. Amy Yasko (Author)
Provides background information on the value and usefullness of genetic testing as well as specific recommendations for analyzing and comprehending gene mutations.
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Muscle Gene Therapy: Methods and Protocols (Methods in Molecular Biology)
by Dongsheng Duan (Editor)
Gene therapy offers many conceptual advantages to treat muscle diseases, especially various forms of muscular dystrophies; however, it faces a number of unique challenges, including the need to deliver a therapeutic vector to all muscles throughout the body. In Muscle Gene Therapy: Methods and Protocols, expert researchers in the field present a collection of techniques aimed at bridging the translational gap in muscle gene therapy between the prevalent rodent models and vitally important larger animal models. Divided into three sections, this volume examines basic protocols for optimizing the muscle gene expression cassette and for evaluating the therapeutic outcomes, new developments in muscle gene therapy technology such as adeno-associated viral vector (AAV),...
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Human Gene Mutation (Human Molecular Genetics Series.)
by David N. Cooper (Author), Michael Krawczak (Author)
Globetrotter Travel Packs offer exceptional value for money by combining Guide and Map in a pocket-sized plastic wallet. -- Fresh new series look -- All the information you need on a destination in one handy pack -- Exceptional value for money
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21st Century Genetics Reference Handbook - Guide to Understanding Genetic Conditions, DNA, Mutations, Chromosomal Changes, Genetic Testing, Gene Therapy, Human Genome Project, Genomic Research
by Progressive Management
This unique guide provides authoritative information about genetics and related issues impacting health and medicine:
Cells and DNA * Cells, genes, and chromosomes * How Genes Work * Proteins, cell growth, and cell division * Mutations and Health * Gene mutations, chromosomal changes, and conditions that run in families * Inheriting Genetic Conditions * Inheritance patterns and understanding risk * Genetic Consultation * Finding and visiting a genetic counselor or other genetics professional * Genetic Testing * Benefits, costs, risks, and limitations of genetic testing * Gene Therapy * Experimental techniques, safety, ethics, and availability * The Human Genome Project * Sequencing and understanding the human genome * Genomic Research * Next steps in studying the human...
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Genes, Chromosomes, and Disease: From Simple Traits, to Complex Traits, to Personalized Medicine (FT Press Science)
by Nicholas Wright Gillham (Author)
This very readable overview of the rise and transformations of medical genetics and of the eugenic impulses that have been inspired by the emerging understanding of the genetic basis of many diseases and disabilities is based on a popular nonmajors course, "Social Implications of Genetics," that Gillham gave for many years at Duke University. The book is suitable for use as a text in similar overview courses about genes and social issues or genes and disease. It gives a good overview of the developments and status of this field for a wide range of biomedical researchers, physicians, and students, especially those interested in the prospects for the new, genetics-based personalized medicine.
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Gene Discovery for Disease Models
by Weikuan Gu (Editor), Yongjun Wang (Editor)
This book provides readers with new paradigms on the mutation discovery in the post-genome era. The completion of human and other genome sequencing, along with other new technologies, such as mutation analysis and microarray, has dramatically accelerated the progress in positional cloning of genes from mutated models. In 2002, the Mouse Genome Sequencing Consortium stated that “The availability of an annotated mouse genome sequence now provides the most efficient tool yet in the gene hunter's toolkit. One can move directly from genetic mapping to identification of candidate genes, and the experimental process is reduced to PCR amplification and sequencing of exons and other conserved elements in the candidate interval. With this streamlined protocol, it is anticipated that many...
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Lewin's Genes X
by Jocelyn E. Krebs (Author), Elliott S. Goldstein (Author), Stephen T. Kilpatrick (Author)
The field of molecular biology and molecular genetics is rapidly changing with new data acquired daily and new insights into well-studied processes presented on a scale of weeks or months rather than years. For decades Lewin's GENES has provided the teaching community with the most cutting edge presentation of molecular biology and molecular genetics, covering gene structure, sequencing, organization, and expression. The latest edition, with a knowledgeable new author team, has enlisted 21 scientists to provide revisions and content updates in their individual fields of expertise, ensuring that Lewin's GENES X is the most current and comprehensive text in the field. Informative new chapters, as well as a reorganization of material, provide a more logical flow of topics and many chapters...
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The Wandering Gene and the Indian Princess: Race, Religion, and DNA
by Jeff Wheelwright (Author)
A brilliant and emotionally resonant exploration of science and family history.A vibrant young Hispano woman, Shonnie Medina, inherits a breast-cancer mutation known as BRCA1.185delAG. It is a genetic variant characteristic of Jews. The Medinas knew they were descended from Native Americans and Spanish Catholics, but they did not know that they had Jewish ancestry as well. The mutation most likely sprang from Sephardic Jews hounded by the Spanish Inquisition. The discovery of the gene leads to a fascinating investigation of cultural history and modern genetics by Dr. Harry Ostrer and other experts on the DNA of Jewish populations.Set in the isolated San Luis Valley of Colorado, this beautiful and harrowing book tells of the Medina family’s five-hundred-year passage from medieval Spain...
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