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Absence of rearrangements in the BRCA2 gene in human cancers

  • S. F. Chin
  • , Q. Wang
  • , A. Puisieux
  • , C. Caldas*
  • *Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

6 Scopus citations

Abstract

Mutations of BRCA2 in sporadic breast and ovarian carcinomas are exceedingly rare. This led to the suggestion that large genomic rearrangements could be involved. We performed Southern blots in genomic DNA from 130 primary breast cancers and 83 cancer cell lines (breast, ovarian, pancreatic and small cell lung carcinomas) and found no genomic rearrangements. These results suggest that a gene other than BRCA2 is the target of the frequent 13q12.3 allelic deletions in human cancers.

Original languageEnglish
Pages (from-to)193-195
Number of pages3
JournalBritish Journal of Cancer
Volume84
Issue number2
DOIs
StatePublished - 2001
Externally publishedYes

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

Keywords

  • BRCA2
  • Deletion
  • Human cancers
  • Rearrangement
  • Southern blot

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