Literature DB >> 11605036

Up-regulation of neuroendocrine differentiation in prostate cancer after androgen deprivation therapy, degree and androgen independence.

T Ito1, S Yamamoto, Y Ohno, K Namiki, T Aizawa, A Akiyama, M Tachibana.   

Abstract

The up-regulation of neuroendocrine (NE) differentiation after hormonal therapy, as well as the relationship between the degree of NE differentiation and androgen independence was investigated. One hundred and thirty-seven whole prostate specimens that were derived from surgery and autopsy (group A: no hormonal therapy, 44 patients; group B: with hormonal therapy less than 12 months, 25 patients; group C: with hormonal therapy more than 13 months, 68 patients) were studied. Neuroendocrine differentiation was evaluated by immunostaining with chromogranin A. The degree of NE differentiation was evaluated by the percentage area of positive NE cell expression (grade 0, negative; grade 1, 1-33%; grade 2, 34-66%; grade 3, 67-100%). The degree of NE differentiation was compared in androgen-independent and -dependent tumors in group C. Neuroendocrine differentiation was expressed as 31.8% in group A, 44% in group B and 70.5% in group C (p<0.001, Chi-squared test). Group C included 20 androgen-independent cases in which 3 cases were grade 0, 2 were grade 1, 6 were grade 2 and 9 were grade 3. Conversely, for androgen-dependent cases, there were 16, 16, 11 and 5 cases, respectively. Neuroendocrine cells, whether positive or not, alone was not significantly different (p=0.124, Chi-squared test); however, the percentage area of positive NE cell expression was significantly different between the androgen-independent and -dependent tumors (p=0.0044, Chi-squared test). Hormonal therapy may play an important role in the up-regulation of NE differentiation. As well as NE cell expression, whether positive or not, the degree of expression should also be observed to evaluate a poor prognosis, tumor progression and androgen independence.

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Year:  2001        PMID: 11605036     DOI: 10.3892/or.8.6.1221

Source DB:  PubMed          Journal:  Oncol Rep        ISSN: 1021-335X            Impact factor:   3.906


  15 in total

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Authors:  Kyung Park; Zhengming Chen; Theresa Y MacDonald; Javed Siddiqui; Huihui Ye; Andreas Erbersdobler; Maria M Shevchuk; Brian D Robinson; Martin G Sanda; Arul M Chinnaiyan; Himisha Beltran; Mark A Rubin; Juan Miguel Mosquera
Journal:  Hum Pathol       Date:  2014-06-26       Impact factor: 3.466

3.  N-Myc Induces an EZH2-Mediated Transcriptional Program Driving Neuroendocrine Prostate Cancer.

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Journal:  Cancer Cell       Date:  2016-10-10       Impact factor: 31.743

4.  Mash1 expression is induced in neuroendocrine prostate cancer upon the loss of Foxa2.

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5.  Concurrent AURKA and MYCN gene amplifications are harbingers of lethal treatment-related neuroendocrine prostate cancer.

Authors:  Juan Miguel Mosquera; Himisha Beltran; Kyung Park; Theresa Y MacDonald; Brian D Robinson; Scott T Tagawa; Sven Perner; Tarek A Bismar; Andreas Erbersdobler; Rajiv Dhir; Joel B Nelson; David M Nanus; Mark A Rubin
Journal:  Neoplasia       Date:  2013-01       Impact factor: 5.715

6.  Neuroendocrine differentiation in usual-type prostatic adenocarcinoma: Molecular characterization and clinical significance.

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Journal:  Prostate       Date:  2020-07-10       Impact factor: 4.012

Review 7.  Androgen-targeted therapy-induced epithelial mesenchymal plasticity and neuroendocrine transdifferentiation in prostate cancer: an opportunity for intervention.

Authors:  Mannan Nouri; Ellca Ratther; Nataly Stylianou; Colleen C Nelson; Brett G Hollier; Elizabeth D Williams
Journal:  Front Oncol       Date:  2014-12-23       Impact factor: 6.244

8.  Sphingosine kinase-1 is central to androgen-regulated prostate cancer growth and survival.

Authors:  Audrey Dayon; Leyre Brizuela; Claire Martin; Catherine Mazerolles; Nelly Pirot; Nicolas Doumerc; Leonor Nogueira; Muriel Golzio; Justin Teissié; Guy Serre; Pascal Rischmann; Bernard Malavaud; Olivier Cuvillier
Journal:  PLoS One       Date:  2009-11-26       Impact factor: 3.240

9.  REST reduction is essential for hypoxia-induced neuroendocrine differentiation of prostate cancer cells by activating autophagy signaling.

Authors:  Tzu-Ping Lin; Yi-Ting Chang; Sung-Yuan Lee; Mel Campbell; Tien-Chiao Wang; Shu-Huei Shen; Hsiao-Jen Chung; Yen-Hwa Chang; Allen W Chiu; Chin-Chen Pan; Chi-Hung Lin; Cheng-Ying Chu; Hsing-Jien Kung; Chia-Yang Cheng; Pei-Ching Chang
Journal:  Oncotarget       Date:  2016-05-03

10.  GRK3 is a direct target of CREB activation and regulates neuroendocrine differentiation of prostate cancer cells.

Authors:  Meixiang Sang; Mohit Hulsurkar; Xiaochong Zhang; Haiping Song; Dayong Zheng; Yan Zhang; Min Li; Jianming Xu; Songlin Zhang; Michael Ittmann; Wenliang Li
Journal:  Oncotarget       Date:  2016-07-19
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