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PMID: 2569708 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Amplification and rearrangement of c-erb B proto-oncogenes in cancer of human female genital tract.

Oncogene ·Vol. 4 ·No. 8 ·1989-08-00 ·Pages 985-9

Zhang X, Silva E, Gershenson D, Hung MC

Abstract

There are two genes related to the v-erb B oncogene in the human genome. The c-erb B-1 gene encodes the epidermal growth factor receptor (EGF-r), and the c-erb B-2/neu gene encodes a receptor-like protein very similar to, but distinct from the EGF-r. Southern blot analysis of DNAs from 15 fresh human ovarian carcinomas showed that the c-erb B-2/neu gene was amplified in 3 tumors. The c-erb B-1/EGF-r gene was not amplified. However, in one case of adenocarcinoma of uterine endometrium, the c-erb B-1/EGF-r was found to be rearranged in the 5' region of this gene. The genomic structure of the rearranged c-erb B-1/EGF-r gene is similar to those found in the chicken v-erb B oncogene, which produces a truncated form of the EGF-r. The results suggest that amplification of the c-erb B-2/neu gene may play a role in the pathogenesis of ovarian carcinoma. Further, the human c-erb B-1/EGF-r gene in adenocarcinoma of uterine endometrium may be activated by a similar mechanism as that in the chicken v-erb B oncogene.

MeSH Terms
Adenocarcinoma/genetics Carcinoma/genetics DNA, Neoplasm/genetics ErbB Receptors Female Gene Amplification Humans Ovarian Neoplasms/genetics Proto-Oncogene Proteins/genetics Proto-Oncogenes Receptor, ErbB-2 Uterine Neoplasms/genetics
Chemicals
DNA, Neoplasm Proto-Oncogene Proteins ErbB Receptors Receptor, ErbB-2
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Zhang X
University of Texas, M.D. Anderson Cancer Center, Houston 77030.
Silva E
Gershenson D
Hung M C
Article Info
Journal
Oncogene
Abbr.
Oncogene
ISSN
0950-9232
Published
1989-08-00
Pages
985-9
Language
English
Region
England
NLM ID
8711562
Subset
IM
Grants
NCI NIH HHS · CA 45265 · United States
NCRR NIH HHS · RR-5511 · United States
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