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PMID: 10822368 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, Non-P.H.S. Research Support, U.S. Gov't, P.H.S.

Induction of human Cdc37 in prostate cancer correlates with the ability of targeted Cdc37 expression to promote prostatic hyperplasia.

Oncogene ·Vol. 19 ·No. 18 ·2000-04-27 ·Pages 2186-93

Stepanova L, Yang G, DeMayo F, Wheeler TM, Finegold M, Thompson TC, Harper JW

Abstract

The Cdc37 gene encodes a 50 kDa protein which targets intrinsically unstable oncoprotein kinases such as Cdk4, Raf-1, and src to the molecular chaperone Hsp90. This activity is thought to play an important role in the establishment of signaling pathways controlling cell proliferation. The budding yeast Cdc37 homolog is required for cell division and mammalian Cdc37 is expressed in proliferative zones during embryonic development and in adult tissues, consistent with a positive role in proliferation. Here we report that human prostatic tumors, neoplasias and certain pre-malignant lesions display increased Cdc37 expression, suggesting an important and early role for Cdc37 in prostatic transformation. To test the consequences of increased Cdc37 levels, transgenic mice expressing Cdc37 in the prostate were generated. These mice displayed a wide range of growth-related abnormalities including prostatic epithelial cell hyperplasia and dysplasia. These data suggest that the expression of Cdc37 may promote inappropriate proliferation and may be an important early step in the development of human prostate cancer.

MeSH Terms
Animals Cell Cycle Proteins/biosynthesis,genetics Cell Transformation, Neoplastic Chaperonins Drosophila Proteins Epithelium/pathology Humans Male Mice Mice, Transgenic Molecular Chaperones Neoplasm Proteins/biosynthesis,genetics Prostatic Hyperplasia/etiology Prostatic Neoplasms/etiology Recombinant Proteins/biosynthesis
Chemicals
CDC37 protein, human Cdc37 protein, mouse Cell Cycle Proteins Drosophila Proteins Molecular Chaperones Neoplasm Proteins Recombinant Proteins Chaperonins
Authors & Affiliations
7 authors, click to expand affiliations / ORCID
Stepanova L
Verna and Marrs McLean Department of Biochemistry and Molecular Biology, Baylor College of Medicine, Houston, Texas 77030, USA.
Yang G
DeMayo F
Wheeler T M
Finegold M
Thompson T C
Harper J W
Article Info
Journal
Oncogene
Abbr.
Oncogene
ISSN
0950-9232
Published
2000-04-27
Pages
2186-93
Language
English
Region
England
NLM ID
8711562
Subset
IM
Grants
NIGMS NIH HHS · GM54137 · United States
PHS HHS · P50-58204 · United States
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