Familial cancer and oncogenic factors

M. Ohmori, S. Tomita, D. Matuzoe, Takehiko Sasazuki

Research output: Contribution to journalReview article

Abstract

The recent remarkable progress in molecular biology has revealed that various kinds of genetic alteration occur in cancers. Recently, many genes that cause hereditary cancer have been identified. For example, hMSH2 and hMLH1, which are known as DNA mismatch repair genes have been found to cause HNPCC (hereditary non-poliposis colorectal cancer). Mutation of RET oncogene has been recognized in the families of MEN (multiple endocrine neoplasia) type II. Mutations of the tumor suppressor genes are the most common changes in the genes of familial cancer. BRCA1 and BRCA2 are tumor suppressor genes that have recently been identified as familial breast and ovarian cancer, familial breast cancer genes. This paper reviewed the hereditary cancer families in which genetic alterations have been revealed and the recent progress in mapping and cloning of familial breast cancer candidate genes which have not been identified.

Original languageEnglish
Pages (from-to)395-400
Number of pages6
JournalJapanese Journal of Cancer and Chemotherapy
Volume23
Issue number4
Publication statusPublished - May 2 1996

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All Science Journal Classification (ASJC) codes

  • Oncology
  • Cancer Research

Cite this

Ohmori, M., Tomita, S., Matuzoe, D., & Sasazuki, T. (1996). Familial cancer and oncogenic factors. Japanese Journal of Cancer and Chemotherapy, 23(4), 395-400.