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PMID: 8988055 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Interleukin-6 as a paracrine and autocrine growth factor in human prostatic carcinoma cells in vitro.

Cancer research ·Vol. 57 ·No. 1 ·1997-01-01 ·Pages 141-6

Okamoto M, Lee C, Oyasu R

Abstract

Interleukin (IL)-6 plays a significant role in genitourinary carcinomas. The present study was conducted to define the role of IL-6 in the growth of prostatic carcinoma and benign prostatic hyperplasia (BPH). An in vitro experiment was carried out using human prostatic carcinoma cell lines (LNCaP, which is androgen sensitive and slow growing, and DU145 and PC3, which are androgen insensitive and fast growing), and primary human epithelial and stromal cells derived from BPH. Cells were treated with recombinant human IL-6 or conditioned medium (CM) derived from the above cultured cells to identify possible paracrine and autocrine pathways. LNCaP was clearly responsive to exogenous IL-6 and to the CM derived from stromal cells, but not to the CM from LNCaP cells (P < 0.001). DU145 and PC3 were slightly stimulated to grow by exogenous IL-6 and the CM derived from both stromal and respective homologous cells (P < 0.01). In contrast, BPH-derived epithelial cells showed little or no response to IL-6. The stimulatory effect of CM on prostatic carcinoma cells was significantly reduced by the addition of anti-IL-6 antibody to the culture medium. Furthermore, the growth of DU145 and PC3 in serum-free medium was also inhibited by anti-IL-6 antibody (P < 0.001). All cell lines tested, except for LNCaP, secreted IL-6 into the culture medium. Results of reverse transcriptase-PCR analysis indicated that IL-6 receptor mRNA was present in all carcinoma cell lines but not in epithelial cells or stromal cells derived from BPH. These results suggest that IL-6 functions as a paracrine growth factor for LNCaP and as an autocrine growth factor for DU145 and PC3, but it has no stimulatory effect on epithelial cells derived from BPH.

MeSH Terms
Antibodies, Anti-Idiotypic/pharmacology Antigens, CD/metabolism Cell Division/drug effects Culture Media, Conditioned/pharmacology Cytokine Receptor gp130 Humans Interleukin-6/immunology,metabolism,pharmacology Lipopolysaccharides/pharmacology Male Membrane Glycoproteins/metabolism Neoplasm Proteins/metabolism Prostatic Hyperplasia/metabolism,pathology Prostatic Neoplasms/metabolism,pathology RNA, Messenger/metabolism Receptors, Interleukin/metabolism Receptors, Interleukin-6 Tumor Cells, Cultured/drug effects
Chemicals
Antibodies, Anti-Idiotypic Antigens, CD Culture Media, Conditioned IL6ST protein, human Interleukin-6 Lipopolysaccharides Membrane Glycoproteins Neoplasm Proteins RNA, Messenger Receptors, Interleukin Receptors, Interleukin-6 Cytokine Receptor gp130
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Okamoto M
Department of Pathology, Northwestern University Medical School, Chicago, Illinois 60611-3008, USA.
Lee C
Oyasu R
Article Info
Journal
Cancer research
Abbr.
Cancer Res
ISSN
0008-5472
Published
1997-01-01
Pages
141-6
Language
English
Region
United States
NLM ID
2984705R
Subset
IM
Grants
NCI NIH HHS · CA 14649 · United States
NCI NIH HHS · CA33511 · United States
NCI NIH HHS · CA69851 · United States
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