Literature DB >> 7855002

Cellular proliferation in prostatic adenocarcinoma as assessed by bromodeoxyuridine uptake and Ki-67 and PCNA expression.

M L Cher1, K Chew, W Rosenau, P R Carroll.   

Abstract

Prostatic carcinomas vary in their biological potential, even when stratified by grade and stage. Measurement of cellular proliferation by various methods has been shown to correlate with outcome for several human cancers, including prostatic carcinoma. Uptake of bromodeoxyuridine (BrdUrd), a thymidine analogue, has been accepted as a measure of cellular proliferative rate. However, the technique is somewhat complex, requiring incubation with fresh tissue. We compared cellular proliferation as measured by BrdUrd uptake with two more simple immunohistochemical methods in 44 prostatic adenocarcinoma specimens and correlated the results with standard clinical parameters. The tissue was obtained via needle biopsy, channel transurethral resection, and radical prostatectomy. Specimens were incubated in vitro with BrdUrd and then fixed and paraffin embedded. Sections were immunohistochemically stained with antibodies to BrdUrd, proliferating cell nuclear antigen (PCNA), and Ki-67. At least 1,000 cells were scored, and a labeling index (LI) was calculated (number of positive cells/total number of cells). The mean LI determined by all three indices was low (BrdUrd = 3.0, PCNA = 7.0, Ki-67 = 3.4), consistent with the knowledge that prostatic tumors grow slowly. In 36 patients who had not been treated at the time of analysis, the LI as determined by all three methods correlated well with clinical stage and pathological grade. Furthermore, the LIs discriminated between those with tumor confined to the prostate and those with extension to the seminal vesicles, lymph nodes, or bone (P = 0.003, 0.004, 0.008 for BrdUrd, PCNA, and Ki-67, respectively). The LIs for PCNA and Ki-67 correlated well with that for BrdUrd (r = 0.84; r = 0.85), while the LIs for Ki-67 and PCNA correlated slightly less well with each other (r = 0.78). PCNA and Ki-67 expression appear to reflect essentially the same biological process as BrdUrd uptake. Either can substitute for BrdUrd as a measure of cellular proliferation, and Ki-67 seems to offer the fewest technical problems.

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Year:  1995        PMID: 7855002     DOI: 10.1002/pros.2990260205

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


  15 in total

1.  Ki-67 expression in early prostate cancer and associated pathological lesions.

Authors:  M R Feneley; M P Young; C Chinyama; R S Kirby; M C Parkinson
Journal:  J Clin Pathol       Date:  1996-09       Impact factor: 3.411

2.  Role of active surveillance in the management of localized prostate cancer.

Authors:  Allison S Glass; Matthew R Cooperberg; Maxwell V Meng; Peter R Carroll
Journal:  J Natl Cancer Inst Monogr       Date:  2012-12

3.  Overexpression of SMARCA5 correlates with cell proliferation and migration in breast cancer.

Authors:  Quanxiu Jin; Xiaoyun Mao; Bo Li; Shu Guan; Fan Yao; Feng Jin
Journal:  Tumour Biol       Date:  2014-11-07

4.  Prostate Cancer - Old Problems and New Approaches. (Part II. Diagnostic and Prognostic Markers, Pathology and Biological Aspects).

Authors:  Kenneth V Honn; Amer Aref; Yong Q Chen; Michael L Cher; John D Crissman; Jeffrey D Forman; Xiang Gao; David Grignon; Maha Hussain; Arthur T Porter; Edson J Pontes; Bruce Redman; Wael Sakr; Richard Severson; Dean G Tang; David P Wood
Journal:  Pathol Oncol Res       Date:  1996       Impact factor: 3.201

5.  Prostate Cancer Old Problems and New Approaches. Part III. Prevention and Treatment.

Authors:  Kenneth V Honn; Amer Aref; Yong Q Chen; Michael L Cher; John D Crissman; Jeffrey D Forman; Xiang Gao; David Grignon; Maha Hussain; Arthur T Porter; J.Edson Pontes; Bruce Redman; Wael Sakr; Richard Severson; Dean G Tang; David P Wood
Journal:  Pathol Oncol Res       Date:  1996       Impact factor: 3.201

6.  Differential effects of resveratrol on androgen-responsive LNCaP human prostate cancer cells in vitro and in vivo.

Authors:  Thomas T Y Wang; Tamaro S Hudson; Tien-Chung Wang; Connie M Remsberg; Neal M Davies; Yoko Takahashi; Young S Kim; Harold Seifried; Bryan T Vinyard; Susan N Perkins; Stephen D Hursting
Journal:  Carcinogenesis       Date:  2008-06-26       Impact factor: 4.944

7.  Long-term assessment of prostate cancer progression free survival: evaluation of pathological parameters, nuclear shape and molecular biomarkers of pathogenesis.

Authors:  Robert W Veltri; Sumit Isharwal; M Craig Miller; Jonathan I Epstein; Leslie A Mangold; Elizabeth Humphreys; Alan W Partin
Journal:  Prostate       Date:  2008-12-01       Impact factor: 4.104

8.  DNA replication regulation protein Mcm7 as a marker of proliferation in prostate cancer.

Authors:  V Padmanabhan; P Callas; G Philips; T D Trainer; B G Beatty
Journal:  J Clin Pathol       Date:  2004-10       Impact factor: 3.411

9.  Adipose tissue-derived mesenchymal stem cells expressing prodrug-converting enzyme inhibit human prostate tumor growth.

Authors:  Ilaria T Cavarretta; Veronika Altanerova; Miroslava Matuskova; Lucia Kucerova; Zoran Culig; Cestmir Altaner
Journal:  Mol Ther       Date:  2009-10-20       Impact factor: 11.454

10.  Exogenous thyroid hormone affects myoepithelium and proliferation in the developing rat parotid gland.

Authors:  R Ikeda; S Aiyama; R S Redman
Journal:  Biotech Histochem       Date:  2009-12       Impact factor: 1.718

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