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Presence of two members of c-erbA receptor gene family (c-erbA beta and c-erbA2) in smallest region of somatic homozygosity on chromosome 3p21-p25 in human breast carcinoma.

Abstract
The loss of heterozygosity of genes on the short arm of chromosome 3 (3p) in human breast carcinomas occurs in a region involved in other malignancies, including renal cell carcinoma, lung cancers, and von Hippel-Lindau disease. This finding suggests the presence of a gene(s) that plays a crucial role in multiple cancers. In our study of 84 informative (heterozygous) primary breast tumors, 30% showed losses of heterozygosity on chromosome 3. The shortest region of homozygosity in primary human breast tumor is located between the DNF15S2 and RAF1 loci in the 3p21-p25 region on the short arm of chromosome 3. This region includes at least two members of the c-erbA steroid/thyroid hormone receptor family (c-erbA beta and c-erbA2) that may be of special relevance to breast cancer. Furthermore, tumors with a loss of heterozygosity of genes on chromosome 3 were previously reported to have frequent allelic deletions on chromosome 11p and amplification of the c-myc proto-oncogene. These results highlight the occurrence of multiple genetic alterations in breast tumors.
AuthorsI U Ali, R Lidereau, R Callahan
JournalJournal of the National Cancer Institute (J Natl Cancer Inst) Vol. 81 Issue 23 Pg. 1815-20 (Dec 06 1989) ISSN: 0027-8874 [Print] United States
PMID2573734 (Publication Type: Journal Article)
Chemical References
  • DNA, Neoplasm
  • MAS1 protein, human
  • Proto-Oncogene Mas
  • Proto-Oncogene Proteins
  • Receptors, Thyroid Hormone
Topics
  • Breast Neoplasms (genetics)
  • Carcinoma, Intraductal, Noninfiltrating (genetics)
  • Chromosome Deletion
  • Chromosome Mapping
  • Chromosomes, Human, Pair 3
  • DNA, Neoplasm (analysis)
  • Female
  • Genotype
  • Humans
  • Polymorphism, Restriction Fragment Length
  • Proto-Oncogene Mas
  • Proto-Oncogene Proteins (analysis)
  • Receptors, Thyroid Hormone

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