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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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Gene: Gene. History of genetics, Mendelian inheritance, Gene expression, Genetic code, Mutation, Gene targeting, The Selfish Gene, Copy number variation, ... Gene- centered view of evolution
by Frederic P. Miller (Editor), Agnes F. Vandome (Editor), John McBrewster (Editor)
Gene. History of genetics, Mendelian inheritance, Gene expression, Genetic code, Mutation, Gene targeting, The Selfish Gene, Copy number variation, DNA, Epigenetics, Gene- centered view of evolution, Gene therapy, Genetic algorithm, Genetics, Genome, Genomics, List of human genes, Meme, Pseudogene, Predictive medicine
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ABC News Nightline Confronting a Genetic Legacy
Imagine you were told that you carry a gene that makes it all but certain you will one day get breast cancer, ovarian cancer or both. What would you do? Jessica Queller, a 35-year-old writer for the hit series "Gilmore Girls," has had to answer that question. In 2004, she found out that she carries the BRCA1 gene mutation, or, the breast cancer gene. According to one study, possessing that gene means she has an 85 percent chance of developing breast cancer before the age of 70 and a 50 percent chance of developing it before the age of 50. Queller took the test because her mother had recently died of ovarian cancer, and several years earlier had fought and beaten breast cancer. Queller now knows what her mother never did, and now she is left in a place where modern science has told her...
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Mutation linked to some cases of Parkinson's: identifying gene raises ethical questions about its use in testing, given the lack of preventive therapy.(Neuropsychiatric ... An article from: Clinical Psychiatry News
by Christine Kilgore (Author)
This digital document is an article from Clinical Psychiatry News, published by International Medical News Group on April 1, 2005. The length of the article is 933 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: Mutation linked to some cases of Parkinson's: identifying gene raises ethical questions about its use in testing, given the lack of preventive therapy.(Neuropsychiatric Medicine) Author: Christine Kilgore Publication: Clinical Psychiatry News (Magazine/Journal) Date: April 1, 2005 Publisher: International Medical News Group Volume: 33 Issue: 4 Page:...
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Limited Family Structure and BRCA Gene Mutation Status in Single Cases of Breast Cancer / Identifying Widely Covered Drugs and Drug Coverage Variation Among Medicare Part D Formularies (JAMA: The Journal of the American Medical Association, Volume 297, Number 23, June 20, 2007)
by J. N. Weitzel (Author)
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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 mammography.(Women's ... 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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![Mouse lymphoma thymidine kinase gene mutation assay: Meeting of the International Workshop on Genotoxicity Testing, San Francisco, 2005, recommendations ... Toxicology and Environmental Mutagenesis]](http://ecx.images-amazon.com/images/I/51VRJGWFK9L._SL160_.jpg)
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Mouse lymphoma thymidine kinase gene mutation assay: Meeting of the International Workshop on Genotoxicity Testing, San Francisco, 2005, recommendations ... Toxicology and Environmental Mutagenesis]
by M.M. Moore (Author), M. Honma (Author), J. Clements (Author), G. Bolcsfoldi (Author)
This digital document is a journal article from Mut.Res.-Genetic Toxicology and Environmental Mutagenesis, published by Elsevier in 2007. The article is delivered in HTML format and is available in your Amazon.com Media Library immediately after purchase. You can view it with any web browser.
Description: The Mouse Lymphoma Assay (MLA) Workgroup of the International Workshop on Genotoxicity Testing (IWGT), comprised of experts from Japan, Europe and the United States, met on September 9, 2005, in San Francisco, CA, USA. This meeting of the MLA Workgroup was devoted to reaching a consensus on issues involved with 24-h treatment. Recommendations were made concerning the acceptable values for the negative/solvent control (mutant frequency, cloning efficiency and suspension growth)...
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![American Cancer Society Film: Time is Life (1949) [DVD]](http://ecx.images-amazon.com/images/I/416uIWyVduL._SL160_.jpg)
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American Cancer Society Film: Time is Life (1949) [DVD]
Time is Life highlights the importance of time in combating the second highest cause of death in the world, cancer. The film also underscores the efforts of the American Cancer Society towards the alleviation, if not elimination, of cancer in the American society. The film starts with Mary Bronson being stressed out with the possibility of having a cancer. Cancer is not given proper attention by the public so it causes insurmountable effects on people in the society. Cancer chooses no one. In addition, the film gives conveying figures on cancer fatalities in the United States saying that one in every eight American has cancer. The film has also mentioned that cancer has killed more Americans than the slaughter at the Pearl Harbor and Tokyo Bay during World War Two. The film also dispels...
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Frequency of the 35delG mutation in the GJB2 gene in samples of European, Asian, and African Brazilians.: An article from: Human Biology
by C.A. Oliveira (Author), F. Alexandrino (Author), K. Abe-Sandes (Author), W.A. Silva (Author), A.T. Maciel-Guerra (Author), L.A. Magna (Author), E.L. Sartorato (Author)
This digital document is an article from Human Biology, published by Wayne State University Press on April 1, 2004. The length of the article is 1423 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.
From the author: KEY WORDS: GJB2, BRAZILIAN POPULATION, CONGENITAL DEAFNESS
Citation Details Title: Frequency of the 35delG mutation in the GJB2 gene in samples of European, Asian, and African Brazilians. Author: C.A. Oliveira Publication: Human Biology (Refereed) Date: April 1, 2004 Publisher: Wayne State University Press Volume: 76 Issue: 2 Page: 313(4)
Distributed by...
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Screening of APOB gene mutations in subjects with clinical diagnosis of familial hypercholesterolemia.: An article from: Human Biology
by Erardo Merino-Ibarra (Author), Sergio Castillo (Author), Pilar Mozas (Author), Ana Cenarro (Author), Esperanza Martorell (Author), Jose Luis Diaz (Author), Manuel Suarez-Tembra (Author), Rodrigo Alonso (Author), Fernando Civeira (Author), Pedro Mata (Author), Miguel Pocovi (Author)
This digital document is an article from Human Biology, published by Thomson Gale on October 1, 2005. The length of the article is 4221 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.
From the author: KEY WORDS: FAMILIAL DEFECTIVE APOB, AUTOSOMAL DOMINANT MONOGENIC HYPERCHOLESTEROLEMIA (ADMH), HYPERCHOLESTEROLEMIA, APOB, LDLR, R3500Q MUTATION, T3552T MUTATION, SSCP (SINGLE-STRAND CONFORMATION POLYMORPHISM) ANALYSIS, SPAIN.
Citation Details Title: Screening of APOB gene mutations in subjects with clinical diagnosis of familial hypercholesterolemia. Author: Erardo...
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657del5 mutation of the Nijmegen breakage syndrome gene (NBS1) in the Turkish population.(Author Abstract): An article from: Human Biology
by Mustafa Tekin (Author), Duygu Akcayoz (Author), Canan Ucar (Author), Huseyin Gulen (Author), Nejat Akar (Author)
This digital document is an article from Human Biology, published by Thomson Gale on June 1, 2005. The length of the article is 1366 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.
From the author: KEY WORDS: FOUNDER EFFECT, NIJMEGEN BREAKAGE SYNDROME, NBS1, SLAVS, TURKS.
Citation Details Title: 657del5 mutation of the Nijmegen breakage syndrome gene (NBS1) in the Turkish population.(Author Abstract) Author: Mustafa Tekin Publication: Human Biology (Magazine/Journal) Date: June 1, 2005 Publisher: Thomson Gale Volume: 77 Issue: 3 Page: 393(5)
Article Type: Author...
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