Literature DB >> 17126478

NeuroD1 expression in human prostate cancer: can it contribute to neuroendocrine differentiation comprehension?

Luca Cindolo1, Renato Franco, Monica Cantile, Giulia Schiavo, Giuseppina Liguori, Paolo Chiodini, Liugi Salzano, Riccardo Autorino, Arturo Di Blasi, Mario Falsaperla, Elisa Feudale, Gerardo Botti, Antonio Gallo, Clemente Cillo.   

Abstract

OBJECTIVES: Neuroendocrine differentiation is a common feature of prostate cancer (pCA). NeuroD1 is a neuronal transcription factor able to convert epithelial cells into neurons. The aim of the study is to investigate NeuroD1 expression and compare it with chromogranin-A, synaptophysin, and CD56 staining in human prostate cell lines and surgical specimens.
METHODS: We detected NeuroD1 gene expression, by duplex reverse transcriptase-polymerase chain reaction, in primary human prostate fibroblasts, in EPN, LNCaP, DU145, and PC3 cell lines before and after cAMP exposure, in 6 BPH and 11 pCA samples. Thereafter 166 paraffin sections from normal and neoplastic prostates were stained with NeuroD1, chromogranin-A, synaptophysin, and CD56 antibodies. The relationships between chromogranin-A and NeuroD1 and clinicopathologic parameters were evaluated by multivariate logistic regression analysis.
RESULTS: NeuroD1 is inactive in baseline prostate cell lines and BPHs, whereas it is actively expressed in cAMP-treated EPN, PC3, and DU145 cells. In our surgical series, positive chromogranin-A, synaptophysin, CD56, and NeuroD1 staining was detected in 26.5%, 4.3%, 3.1%, and 35.5%, respectively (difference between chromogranin-A and NeuroD1: p<0.05). The multivariate analysis showed a strong association between chromogranin-A and microscopic perineural invasion (OR: 2.49; 95%CI, 0.85-7.32; p=0.097) and a high primary Gleason score (OR: 1.96; 95%CI, 1.14-3.39; p=0.015), whereas NeuroD1 expression strictly correlated to microscopic perineural invasion (OR: 2.97; 95%CI, 1.05-8.41; p=0.04).
CONCLUSIONS: Expression of NeuroD1 versus chromogranin-A is more frequent in pCA, and correlates to increased indicators of malignancy in moderately to poorly differentiated pCA, and could be involved in the pathophysiology of the neuroendocrine differentiation of pCA.

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Year:  2006        PMID: 17126478     DOI: 10.1016/j.eururo.2006.11.030

Source DB:  PubMed          Journal:  Eur Urol        ISSN: 0302-2838            Impact factor:   20.096


  10 in total

1.  NeuroD1 promotes tumor cell proliferation and tumorigenesis by directly activating the pentose phosphate pathway in colorectal carcinoma.

Authors:  Zhuolin Li; Yuxin He; Yanjun Li; Juan Li; Hezhao Zhao; Guanbing Song; Makoto Miyagishi; Shourong Wu; Vivi Kasim
Journal:  Oncogene       Date:  2021-10-16       Impact factor: 9.867

2.  Oct4A is expressed by a subpopulation of prostate neuroendocrine cells.

Authors:  Paula Sotomayor; Alejandro Godoy; Gary J Smith; Wendy J Huss
Journal:  Prostate       Date:  2009-03-01       Impact factor: 4.104

3.  NeuroD1 regulates survival and migration of neuroendocrine lung carcinomas via signaling molecules TrkB and NCAM.

Authors:  Jihan K Osborne; Jill E Larsen; Misty D Shields; Joshua X Gonzales; David S Shames; Mitsuo Sato; Ashwinikumar Kulkarni; Ignacio I Wistuba; Luc Girard; John D Minna; Melanie H Cobb
Journal:  Proc Natl Acad Sci U S A       Date:  2013-04-03       Impact factor: 11.205

4.  Neuroendocrine cancer-specific up-regulating mechanism of insulin-like growth factor binding protein-2 in small cell lung cancer.

Authors:  Takuya Yazawa; Hanako Sato; Hiroaki Shimoyamada; Koji Okudela; Tetsukan Woo; Michihiko Tajiri; Takashi Ogura; Nobuo Ogawa; Takehisa Suzuki; Hideaki Mitsui; Jun Ishii; Chie Miyata; Masashi Sakaeda; Kazuya Goto; Korehito Kashiwagi; Munetaka Masuda; Takashi Takahashi; Hitoshi Kitamura
Journal:  Am J Pathol       Date:  2009-08-13       Impact factor: 4.307

5.  NeuroD1 regulation of migration accompanies the differential sensitivity of neuroendocrine carcinomas to TrkB inhibition.

Authors:  J K Osborne; J E Larsen; J X Gonzales; D S Shames; M Sato; I I Wistuba; L Girard; J D Minna; M H Cobb
Journal:  Oncogenesis       Date:  2013-08-19       Impact factor: 7.485

6.  Cooperation among heterogeneous prostate cancer cells in the bone metastatic niche.

Authors:  K Shahriari; F Shen; A Worrede-Mahdi; Q Liu; Y Gong; F U Garcia; A Fatatis
Journal:  Oncogene       Date:  2016-12-19       Impact factor: 9.867

Review 7.  The Role of Perineural Invasion in Prostate Cancer and Its Prognostic Significance.

Authors:  Yuequn Niu; Sarah Förster; Michael Muders
Journal:  Cancers (Basel)       Date:  2022-08-23       Impact factor: 6.575

Review 8.  Control of IGFBP-2 Expression by Steroids and Peptide Hormones in Vertebrates.

Authors:  Andreas Hoeflich; Elisa Wirthgen; Robert David; Carl Friedrich Classen; Marion Spitschak; Julia Brenmoehl
Journal:  Front Endocrinol (Lausanne)       Date:  2014-04-07       Impact factor: 5.555

9.  The role of high cell density in the promotion of neuroendocrine transdifferentiation of prostate cancer cells.

Authors:  Zuzana Pernicová; Eva Slabáková; Radek Fedr; Šárka Šimečková; Josef Jaroš; Tereza Suchánková; Jan Bouchal; Gvantsa Kharaishvili; Milan Král; Alois Kozubík; Karel Souček
Journal:  Mol Cancer       Date:  2014-05-20       Impact factor: 27.401

10.  Duodenal gangliocytic paraganglioma, a rare entity among GEP-NET: a case report with immunohistochemical and molecular study.

Authors:  Fabiana Tatangelo; Monica Cantile; Alessia Pelella; Nunzia Simona Losito; Giosuè Scognamiglio; Franco Bianco; Andrea Belli; Gerardo Botti
Journal:  Diagn Pathol       Date:  2014-03-12       Impact factor: 2.644

  10 in total

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