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Autocrine regulation of human prostate carcinoma cell proliferation by somatostatin through the modulation of the SH2 domain containing protein tyrosine phosphatase (SHP)-1.

Abstract
The present study was intended to gain additional information on the growth regulation of prostate by somatostatin (SRIF) and the intracellular events involved. The human prostate adenocarcinoma cell lines PC-3 and LNCaP produce SRIF and express subtypes 2 and 5 of SRIF receptors. The secretion of SRIF is related to the proliferative status of these cells; an inverse relationship exists between cell proliferation and the amount of secreted SRIF. Moreover, the growth of PC-3 cells is inhibited by SRIF overexpression and increased by blockage of endogenous SRIF. Coincident with the increase in SRIF secretion, the activity and levels of the SH2 domain containing protein tyrosine phosphatase (SHP)-1, present in PC-3 cells are augmented, but the effect can be partially prevented by neutralization of secreted endogenously SRIF. The activity of SHP-1 is also stimulated by the SRIF analog RC160. Overexpression of SHP-1 induces inhibition of PC-3 cell growth. SHP-1 is also present in normal prostate, benign prostatic hyperplasia, prostatic intraepithelial neoplasia, and well differentiated adenocarcinoma. In contrast, no signal is detected in poorly differentiated prostate cancer. These findings demonstrate that SRIF inhibits PC-3 and LNCaP cell proliferation through an autocrine/paracrine SRIF loop. This effect could be mediated by activation of the tyrosine phosphatase SHP-1 detected in these cells as well as in human prostate and prostate cancer.
AuthorsPedro Darío Zapata, Rosa María Ropero, Ana Montserrat Valencia, Louis Buscail, Jose Ignacio López, Rosa María Martín-Orozco, Juan Carlos Prieto, Javier Angulo, Christiane Susini, Pilar López-Ruiz, Begoña Colás
JournalThe Journal of clinical endocrinology and metabolism (J Clin Endocrinol Metab) Vol. 87 Issue 2 Pg. 915-26 (Feb 2002) ISSN: 0021-972X [Print] United States
PMID11836342 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • Intracellular Signaling Peptides and Proteins
  • Receptors, Somatostatin
  • Somatostatin
  • PTPN11 protein, human
  • PTPN6 protein, human
  • Protein Tyrosine Phosphatase, Non-Receptor Type 11
  • Protein Tyrosine Phosphatase, Non-Receptor Type 6
  • Protein Tyrosine Phosphatases
  • SH2 Domain-Containing Protein Tyrosine Phosphatases
Topics
  • Autocrine Communication (physiology)
  • Carcinoma (pathology)
  • Cell Division (physiology)
  • Humans
  • Intracellular Signaling Peptides and Proteins
  • Male
  • Prostate (enzymology)
  • Prostatic Neoplasms (pathology)
  • Protein Tyrosine Phosphatase, Non-Receptor Type 11
  • Protein Tyrosine Phosphatase, Non-Receptor Type 6
  • Protein Tyrosine Phosphatases (chemistry, physiology)
  • Receptors, Somatostatin (metabolism)
  • SH2 Domain-Containing Protein Tyrosine Phosphatases
  • Somatostatin (metabolism, physiology)
  • Tumor Cells, Cultured
  • src Homology Domains (physiology)

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