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Telomeric DNA: Marker for human prostate cancer development?
Author(s) -
Ozen Mustafa,
Imam S. Ashraf,
Datar Ram H.,
Multani Asha S.,
Narayanan Ram,
Chung Leland W.K.,
von Eschenbach Andrew C.,
Pathak Sen
Publication year - 1998
Publication title -
the prostate
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.295
H-Index - 123
eISSN - 1097-0045
pISSN - 0270-4137
DOI - 10.1002/(sici)1097-0045(19980901)36:4<264::aid-pros8>3.0.co;2-f
Subject(s) - telomerase , telomere , biology , prostate cancer , somatic cell , ribonucleoprotein , cancer research , microbiology and biotechnology , cancer , prostate , cell culture , cell growth , cell division , dna , cell , genetics , gene , rna
BACKGROUND Telomeres that protect chromosomes at both ends are shortened with each somatic cell division through replication‐dependent sequence loss at DNA termini. The chromosomes with shortened telomeres tend to become unstable, leading to cell death. Due largely to reactivation/upregulation of telomerase, a ribonucleoprotein that adds nucleotide sequences onto chromosome ends, cancer cells become immortal and neoplastically transformed. METHODS The purpose of the present study was to study three newly established human prostate cancer cell lines and three prostate‐derived fibroblastic cell cultures at different passages for telomeric DNA signal intensity, telomeric restriction fragment length (TRFL), telomerase activity, and spontaneous apoptotic index. RESULTS Compared with the three fibroblastic cell cultures, the three new prostate cancer cell lines showed: 1) telomerase activity, 2) stronger telomeric signals, 3) relatively longer TRFLs, and 4) much lower apoptotic indices. On the other hand, three fibroblastic cell cultures showed: 1) no telomerase activity, 2) weaker telomeric signals, 3) shorter TRFLs (fibroblasts derived from surrounding tissue of prostate tumor showed intermediate TRFLs), and 4) comparatively higher apoptotic indices. CONCLUSIONS Based on these results, we conclude that telomeric DNA signal intensity, TRFL, and telomerase activity can be used to distinguish prostate cancer cells from adjacent fibroblasts. Prostate 36:264–271, 1998. © 1998 Wiley‐Liss, Inc.