Literature DB >> 10679757

Immunohistochemical staining for DNA topoisomerase II-alpha in benign, premalignant, and malignant lesions of the prostate.

J H Willman1, J A Holden.   

Abstract

BACKGROUND: The DNA topoisomerase II-alpha (topo II-alpha)-targeting drug etoposide was recently shown to be an active agent in the combined chemotherapy of hormone-insensitive prostatic carcinoma. Aside from being the molecular target of etoposide, topo II-alpha is also a cell proliferation marker. Much experimental data indicate that cells sensitive to topo II-targeting chemotherapeutic drugs are rapidly proliferating and show elevated topo II expression. There is little information concerning topo II expression in lesions of the prostate.
METHODS: Paraffin blocks from cases of invasive prostatic carcinoma, prostatic intraepithelial neoplasia, and prostatic nodular hyperplasia were retrieved from the surgical pathology files at the University of Utah Health Sciences Center. Using a new immunohistochemical stain, specific for the alpha isoform of DNA topo II, enzyme expression was evaluated in 54 prostatic adenocarcinomas, 22 lesions of high-grade prostatic intraepithelial neoplasia (PIN), and 10 cases of benign prostatic nodular hyperplasia. Results were semiquantitated by determining for each case a topo II-alpha index, which represented the percent of positively staining cells.
RESULTS: The average topo II-alpha index for well-differentiated prostatic adenocarcinomas (Gleason scores 2-4) was 1.5 +/- 0.9; for moderately differentiated tumors (Gleason scores 5-7), 3.1 +/- 2.4; and for poorly differentiated tumors (Gleason scores 8-10), 6.7 +/- 5.5. The average topo II-alpha index for all invasive prostatic adenocarcinomas was 4.0 (range, 0-19.0). Benign prostatic nodular hyperplasia had the lowest average topo II-alpha index, of 0.54 (range, 0.2-1.0). The average topo II-alpha index of 2.3 (range, 0-8.6) for high-grade prostatic intraepithelial neoplasia was intermediate between the invasive tumors and benign prostate.
CONCLUSIONS: Topo II-alpha expression in carcinoma of the prostate correlates with Gleason score. The carcinomas with the highest expression of enzyme are more poorly differentiated and have the highest Gleason scores. Prostatic nodular hyperplasia shows little expression of topo II-alpha. Prostatic intraepithelial neoplasia has an average topo II-alpha index intermediate between nodular hyperplasia and carcinoma. Copyright 2000 Wiley-Liss, Inc.

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Year:  2000        PMID: 10679757     DOI: 10.1002/(sici)1097-0045(20000301)42:4<280::aid-pros5>3.0.co;2-p

Source DB:  PubMed          Journal:  Prostate        ISSN: 0270-4137            Impact factor:   4.104


  11 in total

Review 1.  Human topoisomerase II alpha as a prognostic biomarker in cancer chemotherapy.

Authors:  Yousaf Ali; Shafida Abd Hamid
Journal:  Tumour Biol       Date:  2015-10-20

2.  Gene expression changes are age-dependent and lobe-specific in the brown Norway rat model of prostatic hyperplasia.

Authors:  Carlise R Bethel; Jaideep Chaudhary; Matthew D Anway; Terry R Brown
Journal:  Prostate       Date:  2009-06-01       Impact factor: 4.104

3.  Topoisomerase II-alpha expression increases with increasing Gleason score and with hormone insensitivity in prostate carcinoma.

Authors:  C Hughes; A Murphy; C Martin; E Fox; M Ring; O Sheils; B Loftus; J O'Leary
Journal:  J Clin Pathol       Date:  2006-03-23       Impact factor: 3.411

4.  High-grade prostatic intraepithelial neoplasia.

Authors:  Joseph C Klink; Ranko Miocinovic; Cristina Magi Galluzzi; Eric A Klein
Journal:  Korean J Urol       Date:  2012-05-18

5.  Reduction of atherosclerotic lesions in rabbits treated with etoposide associated with cholesterol-rich nanoemulsions.

Authors:  Elaine R Tavares; Fatima R Freitas; Jayme Diament; Raul C Maranhão
Journal:  Int J Nanomedicine       Date:  2011-10-12

6.  Topoisomerase II trapping agent teniposide induces apoptosis and G2/M or S phase arrest of oral squamous cell carcinoma.

Authors:  Jinzhong Li; Wantao Chen; Ping Zhang; Ningyi Li
Journal:  World J Surg Oncol       Date:  2006-07-06       Impact factor: 2.754

7.  AK-I-190, a New Catalytic Inhibitor of Topoisomerase II with Anti-Proliferative and Pro-Apoptotic Activity on Androgen-Negative Prostate Cancer Cells.

Authors:  Kyung-Hwa Jeon; Seojeong Park; Hae Jin Jang; Soo-Yeon Hwang; Aarajana Shrestha; Eung-Seok Lee; Youngjoo Kwon
Journal:  Int J Mol Sci       Date:  2021-10-18       Impact factor: 5.923

8.  Prognostication of prostate cancer based on TOP2A protein and gene assessment: TOP2A in prostate cancer.

Authors:  Marina França de Resende; Samantha Vieira; Ludmilla Thomé Domingos Chinen; Francesco Chiappelli; Francisco Paulo da Fonseca; Gustavo Cardoso Guimarães; Fernando Augusto Soares; Ivan Neves; Simone Pagotty; Peter A Pellionisz; Andre Barkhordarian; Xenia Brant; Rafael Malagoli Rocha
Journal:  J Transl Med       Date:  2013-02-11       Impact factor: 5.531

9.  Topoisomerase 2 Alpha Cooperates with Androgen Receptor to Contribute to Prostate Cancer Progression.

Authors:  J L Schaefer-Klein; Stephen J Murphy; Sarah H Johnson; George Vasmatzis; Irina V Kovtun
Journal:  PLoS One       Date:  2015-11-11       Impact factor: 3.240

10.  SPOP is essential for DNA-protein cross-link repair in prostate cancer cells: SPOP-dependent removal of topoisomerase 2A from the topoisomerase 2A-DNA cleavage complex.

Authors:  Ryuta Watanabe; Masashi Maekawa; Miki Hieda; Tomohiko Taguchi; Noriyoshi Miura; Tadahiko Kikugawa; Takashi Saika; Shigeki Higashiyama
Journal:  Mol Biol Cell       Date:  2020-01-22       Impact factor: 4.138

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