Mutational Processes Molding the Genomes of 21 Breast Cancers

نویسندگان

  • Serena Nik-Zainal
  • Ludmil B. Alexandrov
  • David C. Wedge
  • Peter Van Loo
  • Christopher D. Greenman
  • Keiran Raine
  • David Jones
  • Jonathan Hinton
  • John Marshall
  • Lucy A. Stebbings
  • Andrew Menzies
  • Sancha Martin
  • Kenric Leung
  • Lina Chen
  • Catherine Leroy
  • Manasa Ramakrishna
  • Richard Rance
  • King Wai Lau
  • Laura J. Mudie
  • Ignacio Varela
  • David J. McBride
  • Graham R. Bignell
  • Susanna L. Cooke
  • Adam Shlien
  • John Gamble
  • Ian Whitmore
  • Mark Maddison
  • Patrick S. Tarpey
  • Helen R. Davies
  • Elli Papaemmanuil
  • Philip J. Stephens
  • Stuart McLaren
  • Adam P. Butler
  • Jon W. Teague
  • Göran Jönsson
  • Judy E. Garber
  • Daniel Silver
  • Penelope Miron
  • Aquila Fatima
  • Sandrine Boyault
  • Anita Langerød
  • Andrew Tutt
  • John W.M. Martens
  • Samuel A.J.R. Aparicio
  • Åke Borg
  • Anne Vincent Salomon
  • Gilles Thomas
  • Anne-Lise Børresen-Dale
  • Andrea L. Richardson
  • Michael S. Neuberger
  • P. Andrew Futreal
  • Peter J. Campbell
  • Michael R. Stratton
چکیده

All cancers carry somatic mutations. The patterns of mutation in cancer genomes reflect the DNA damage and repair processes to which cancer cells and their precursors have been exposed. To explore these mechanisms further, we generated catalogs of somatic mutation from 21 breast cancers and applied mathematical methods to extract mutational signatures of the underlying processes. Multiple distinct single- and double-nucleotide substitution signatures were discernible. Cancers with BRCA1 or BRCA2 mutations exhibited a characteristic combination of substitution mutation signatures and a distinctive profile of deletions. Complex relationships between somatic mutation prevalence and transcription were detected. A remarkable phenomenon of localized hypermutation, termed "kataegis," was observed. Regions of kataegis differed between cancers but usually colocalized with somatic rearrangements. Base substitutions in these regions were almost exclusively of cytosine at TpC dinucleotides. The mechanisms underlying most of these mutational signatures are unknown. However, a role for the APOBEC family of cytidine deaminases is proposed.

برای دانلود رایگان متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

منابع مشابه

Detecting presence of mutational signatures in cancer with confidence

Motivation Cancers arise as the result of somatically acquired changes in the DNA of cancer cells. However, in addition to the mutations that confer a growth advantage, cancer genomes accumulate a large number of somatic mutations resulting from normal DNA damage and repair processes as well as carcinogenic exposures or cancer related aberrations of DNA maintenance machinery. These mutagenic pr...

متن کامل

The Life History of 21 Breast Cancers

Cancer evolves dynamically as clonal expansions supersede one another driven by shifting selective pressures, mutational processes, and disrupted cancer genes. These processes mark the genome, such that a cancer's life history is encrypted in the somatic mutations present. We developed algorithms to decipher this narrative and applied them to 21 breast cancers. Mutational processes evolve acros...

متن کامل

A mutational signature in gastric cancer suggests therapeutic strategies

Targeting defects in the DNA repair machinery of neoplastic cells, for example, those due to inactivating BRCA1 and/or BRCA2 mutations, has been used for developing new therapies in certain types of breast, ovarian and pancreatic cancers. Recently, a mutational signature was associated with failure of double-strand DNA break repair by homologous recombination based on its high mutational burden...

متن کامل

Deciphering Signatures of Mutational Processes Operative in Human Cancer

The genome of a cancer cell carries somatic mutations that are the cumulative consequences of the DNA damage and repair processes operative during the cellular lineage between the fertilized egg and the cancer cell. Remarkably, these mutational processes are poorly characterized. Global sequencing initiatives are yielding catalogs of somatic mutations from thousands of cancers, thus providing t...

متن کامل

Use of CRISPR-modified human stem cell organoids to study the origin of mutational signatures in cancer.

Mutational processes underlie cancer initiation and progression. Signatures of these processes in cancer genomes may explain cancer etiology and could hold diagnostic and prognostic value. We developed a strategy that can be used to explore the origin of cancer-associated mutational signatures. We used CRISPR-Cas9 technology to delete key DNA repair genes in human colon organoids, followed by d...

متن کامل

ذخیره در منابع من


  با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید

عنوان ژورنال:

دوره 149  شماره 

صفحات  -

تاریخ انتشار 2012