Objective Recently, many tumor sequencing studies have inferred and reported on mutational signatures, short nucleotide patterns at which particular somatic base substitutions appear more often. A number of signatures reflect biological processes in the patient and factors associated with cancer risk. Our goal is to infer mutational signatures appearing in colon cancer, a cancer for which environmental risk factors vary by cancer subtype, and compare the signatures to those in adult stem cells from normal colon. We also compare the mutational signatures to others in the literature. Results We apply a probabilistic mutation signature model to somatic mutations previously reported for six adult normal colon stem cells and 431 colon adenocarcinomas. We infer six mutational signatures in colon cancer, four being specific to tumors with hypermutation. Just two signatures explained the majority of mutations in the small number of normal aging colon samples. All six signatures are independently identified in a series of 295 Chinese colorectal cancers.
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Univ Ljubljana, Inst Biochem & Mol Genet, Fac Med, Pharmacogenet Lab, Vrazov Trg 2, Ljubljana 1000, Slovenia
Univ Ljubljana, Inst Biochem & Mol Genet, Fac Med, Med Ctr Mol Biol, Vrazov Trg 2, Ljubljana 1000, SloveniaUniv Ljubljana, Inst Biochem & Mol Genet, Fac Med, Pharmacogenet Lab, Vrazov Trg 2, Ljubljana 1000, Slovenia
Dominkus, Pia Puzar
Hudler, Petra
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Univ Ljubljana, Inst Biochem & Mol Genet, Fac Med, Med Ctr Mol Biol, Vrazov Trg 2, Ljubljana 1000, SloveniaUniv Ljubljana, Inst Biochem & Mol Genet, Fac Med, Pharmacogenet Lab, Vrazov Trg 2, Ljubljana 1000, Slovenia
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Korea Adv Inst Sci & Technol, Grad Sch Med Sci & Engn, Daejeon 34141, South KoreaKorea Adv Inst Sci & Technol, Grad Sch Med Sci & Engn, Daejeon 34141, South Korea
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Radboud Univ Nijmegen, Med Ctr, Radboud Inst Mol Life Sci, Dept Human Genet, Nijmegen, NetherlandsRadboud Univ Nijmegen, Med Ctr, Radboud Inst Mol Life Sci, Dept Human Genet, Nijmegen, Netherlands
Grolleman, Judith E.
Diaz-Gay, Marcos
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Univ Barcelona, CIBER Hepat & Digest Dis, August Pi i Sunyer Biomed Res Inst, Gastroenterol Dept,Hosp Clin Barcelona, Barcelona, SpainRadboud Univ Nijmegen, Med Ctr, Radboud Inst Mol Life Sci, Dept Human Genet, Nijmegen, Netherlands
Diaz-Gay, Marcos
Franch-Exposito, Sebastia
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Univ Barcelona, CIBER Hepat & Digest Dis, August Pi i Sunyer Biomed Res Inst, Gastroenterol Dept,Hosp Clin Barcelona, Barcelona, SpainRadboud Univ Nijmegen, Med Ctr, Radboud Inst Mol Life Sci, Dept Human Genet, Nijmegen, Netherlands
Franch-Exposito, Sebastia
Castellvi-Bel, Sergi
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Univ Barcelona, CIBER Hepat & Digest Dis, August Pi i Sunyer Biomed Res Inst, Gastroenterol Dept,Hosp Clin Barcelona, Barcelona, SpainRadboud Univ Nijmegen, Med Ctr, Radboud Inst Mol Life Sci, Dept Human Genet, Nijmegen, Netherlands
Castellvi-Bel, Sergi
de Voer, Richarda M.
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Radboud Univ Nijmegen, Med Ctr, Radboud Inst Mol Life Sci, Dept Human Genet, Nijmegen, NetherlandsRadboud Univ Nijmegen, Med Ctr, Radboud Inst Mol Life Sci, Dept Human Genet, Nijmegen, Netherlands