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Age-related cancer mutations associated with clonal hematopoietic expansion

Several genetic alterations characteristic of leukemia and lymphoma have been detected in the blood of individuals without apparent hematological malignancies. We analyzed blood-derived sequence data from 2,728 individuals within The Cancer Genome Atlas, and discovered 77 blood-specific mutations in...

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Autores principales: Xie, Mingchao, Lu, Charles, Wang, Jiayin, McLellan, Michael D., Johnson, Kimberly J., Wendl, Michael C., McMichael, Joshua F., Schmidt, Heather K., Yellapantula, Venkata, Miller, Christopher A., Ozenberger, Bradley A., Welch, John S., Link, Daniel C., Walter, Matthew J., Mardis, Elaine R., Dipersio, John F., Chen, Feng, Wilson, Richard K., Ley, Timothy J., Ding, Li
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4313872/
https://www.ncbi.nlm.nih.gov/pubmed/25326804
http://dx.doi.org/10.1038/nm.3733
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author Xie, Mingchao
Lu, Charles
Wang, Jiayin
McLellan, Michael D.
Johnson, Kimberly J.
Wendl, Michael C.
McMichael, Joshua F.
Schmidt, Heather K.
Yellapantula, Venkata
Miller, Christopher A.
Ozenberger, Bradley A.
Welch, John S.
Link, Daniel C.
Walter, Matthew J.
Mardis, Elaine R.
Dipersio, John F.
Chen, Feng
Wilson, Richard K.
Ley, Timothy J.
Ding, Li
author_facet Xie, Mingchao
Lu, Charles
Wang, Jiayin
McLellan, Michael D.
Johnson, Kimberly J.
Wendl, Michael C.
McMichael, Joshua F.
Schmidt, Heather K.
Yellapantula, Venkata
Miller, Christopher A.
Ozenberger, Bradley A.
Welch, John S.
Link, Daniel C.
Walter, Matthew J.
Mardis, Elaine R.
Dipersio, John F.
Chen, Feng
Wilson, Richard K.
Ley, Timothy J.
Ding, Li
author_sort Xie, Mingchao
collection PubMed
description Several genetic alterations characteristic of leukemia and lymphoma have been detected in the blood of individuals without apparent hematological malignancies. We analyzed blood-derived sequence data from 2,728 individuals within The Cancer Genome Atlas, and discovered 77 blood-specific mutations in cancer-associated genes, the majority being associated with advanced age. Remarkably, 83% of these mutations were from 19 leukemia/lymphoma-associated genes, and nine were recurrently mutated (DNMT3A, TET2, JAK2, ASXL1, TP53, GNAS, PPM1D, BCORL1 and SF3B1). We identified 14 additional mutations in a very small fraction of blood cells, possibly representing the earliest stages of clonal expansion in hematopoietic stem cells. Comparison of these findings to mutations in hematological malignancies identified several recurrently mutated genes that may be disease initiators. Our analyses show that the blood cells of more than 2% of individuals (5–6% of people older than 70 years) contain mutations that may represent premalignant, initiating events that cause clonal hematopoietic expansion.
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spelling pubmed-43138722015-06-01 Age-related cancer mutations associated with clonal hematopoietic expansion Xie, Mingchao Lu, Charles Wang, Jiayin McLellan, Michael D. Johnson, Kimberly J. Wendl, Michael C. McMichael, Joshua F. Schmidt, Heather K. Yellapantula, Venkata Miller, Christopher A. Ozenberger, Bradley A. Welch, John S. Link, Daniel C. Walter, Matthew J. Mardis, Elaine R. Dipersio, John F. Chen, Feng Wilson, Richard K. Ley, Timothy J. Ding, Li Nat Med Article Several genetic alterations characteristic of leukemia and lymphoma have been detected in the blood of individuals without apparent hematological malignancies. We analyzed blood-derived sequence data from 2,728 individuals within The Cancer Genome Atlas, and discovered 77 blood-specific mutations in cancer-associated genes, the majority being associated with advanced age. Remarkably, 83% of these mutations were from 19 leukemia/lymphoma-associated genes, and nine were recurrently mutated (DNMT3A, TET2, JAK2, ASXL1, TP53, GNAS, PPM1D, BCORL1 and SF3B1). We identified 14 additional mutations in a very small fraction of blood cells, possibly representing the earliest stages of clonal expansion in hematopoietic stem cells. Comparison of these findings to mutations in hematological malignancies identified several recurrently mutated genes that may be disease initiators. Our analyses show that the blood cells of more than 2% of individuals (5–6% of people older than 70 years) contain mutations that may represent premalignant, initiating events that cause clonal hematopoietic expansion. 2014-10-19 2014-12 /pmc/articles/PMC4313872/ /pubmed/25326804 http://dx.doi.org/10.1038/nm.3733 Text en http://www.nature.com/authors/editorial_policies/license.html#terms Users may view, print, copy, and download text and data-mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use:http://www.nature.com/authors/editorial_policies/license.html#terms
spellingShingle Article
Xie, Mingchao
Lu, Charles
Wang, Jiayin
McLellan, Michael D.
Johnson, Kimberly J.
Wendl, Michael C.
McMichael, Joshua F.
Schmidt, Heather K.
Yellapantula, Venkata
Miller, Christopher A.
Ozenberger, Bradley A.
Welch, John S.
Link, Daniel C.
Walter, Matthew J.
Mardis, Elaine R.
Dipersio, John F.
Chen, Feng
Wilson, Richard K.
Ley, Timothy J.
Ding, Li
Age-related cancer mutations associated with clonal hematopoietic expansion
title Age-related cancer mutations associated with clonal hematopoietic expansion
title_full Age-related cancer mutations associated with clonal hematopoietic expansion
title_fullStr Age-related cancer mutations associated with clonal hematopoietic expansion
title_full_unstemmed Age-related cancer mutations associated with clonal hematopoietic expansion
title_short Age-related cancer mutations associated with clonal hematopoietic expansion
title_sort age-related cancer mutations associated with clonal hematopoietic expansion
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4313872/
https://www.ncbi.nlm.nih.gov/pubmed/25326804
http://dx.doi.org/10.1038/nm.3733
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