Proliferative Tumor Doubling Times of Prostatic Carcinoma
Author(s) -
Priya N. Werahera,
L. Michael Glodé,
Francisco G. La Rosa,
M. Scott Lucia,
E. David Crawford,
Kenneth A. Easterday,
Holly Sullivan,
Rameshwar S. Sidhu,
Elizabeth Genova,
Tammy E. Hedlund
Publication year - 2011
Publication title -
prostate cancer
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.377
H-Index - 11
eISSN - 2090-3111
pISSN - 2090-312X
DOI - 10.1155/2011/301850
Subject(s) - doubling time , medicine , prostate cancer , prostatectomy , bromodeoxyuridine , carcinoma , flow cytometry , prostate , biochemical recurrence , cancer , pathology , in vivo , urology , cancer research , oncology , cell , biology , immunology , immunohistochemistry , genetics , microbiology and biotechnology
Prostate cancer (PCa) has a variable biology ranging from latent cancer to extremely aggressive tumors. Proliferative activities of cancers may indicate their biological potential. A flow cytometric assay to calculate maximum proliferative doubling times ( T max ) of PCa in radical prostatectomy specimens after preoperative in vivo bromodeoxyuridine (BrdU) infusion is presented. Only 4/17 specimens had tumors large enough for flow cytometric analysis. The T max of tumors was similar and ranged from 0.6 to 3.6 months. Tumors had calculated doubling times 2- to 25-fold faster than their matched normal tissue. Variations in labeling index and T max were observed within a tumor as well as between different Gleason grades. The observed PSA doubling times (PSA-DT) ranged from 18.4 to 32.0 months, considerably slower than the corresponding T max of tumors involved. While lack of data for apoptotic rates is a limitation, apparent biological differences between latent versus aggressive PCa may be attributable to variations in apoptotic rates of these tumors rather than their cell proliferative rates.
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