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Wang L, Liu X, Kreis W, et al. Involvement of prostate specific antigen in the stimulation of LNCaP cell growth. Oncol Rep. 1996;3(5):911-7doi: 10.3892/or.3.5.911.
Wang, L., Liu, X., Kreis, W., & Budman, D. (1996). Involvement of prostate specific antigen in the stimulation of LNCaP cell growth. Oncology reports, 3(5), 911-7. https://doi.org/10.3892/or.3.5.911
Wang, L, et al. "Involvement of prostate specific antigen in the stimulation of LNCaP cell growth." Oncology reports vol. 3,5 (1996): 911-7. doi: https://doi.org/10.3892/or.3.5.911
Wang L, Liu X, Kreis W, Budman D. Involvement of prostate specific antigen in the stimulation of LNCaP cell growth. Oncol Rep. 1996 Sep;3(5):911-7. doi: 10.3892/or.3.5.911. PMID: 21594481.
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Oncol Rep. 1996 Sep;3(5):911-7. doi: 10.3892/or.3.5.911.

Involvement of prostate specific antigen in the stimulation of LNCaP cell growth.

Oncology reports

L Wang, X Liu, W Kreis, D Budman

Affiliations

  1. N SHORE UNIV HOSP,CORNELL UNIV MED COLL,DEPT MED,MANHASSET,NY 11030.

PMID: 21594481 DOI: 10.3892/or.3.5.911

Abstract

Since its identification in 1979, prostatic specific antigen (PSA) has been used extensively as a serum marker for diagnosis and prognosis of prostate cancer. In addition, PSA is an immunohistochemical marker for the identification of prostatic tissues and cells in histological specimens. PSA is found in normal prostate, benign prostatic hypertrophy (BPH) tissue, in cancer of the prostate, and its metastases as well as in other hormone dependent cancers, such as breast and ovarian carcinoma. However, the importance of PSA as a regulator of cell growth generally has not been appreciated. The role of PSA in the development of prostate or other hormone-dependent cancers has remained unclear. We therefore examined the role of PSA in the control of cell growth using both the PSA positive cell line, LNCaP cells and the PSA negative cell line PC-3 and DU145. LNCaP cell growth was stimulated by the conditioned medium (CM) from LNCaP cells, but not by CM from PC-3 or DU145 cells. No such stimulation was observed when PC-3 or DU145 cells were exposed to CM from LNCaP cells nor from CM produced by their own lines. The stimulation of LNCaP cell growth by its own CM could not be attributed to the high level of insulin-like growth factor binding protein-2 (IGFBP-2) present in the CM since even higher level of IGFBP-2 was also found to be present in CM from both PC-3 and DU145 CMs. High level of PSA and 66 kDa epidermal growth factor (EGF) were present in LNCaP CM as measured by Western blotting. The stimulation of LNCaP cell growth by its own CM was eliminated partially by PSA or EGF antibody. Stimulation of DNA biosynthesis in LNCaP cells by LNCaP CM or pure PSA was also observed. These data indicate that PSA and EGF are involved in the growth regulation of PSA positive LNCaP cell line.

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