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Human renal cell cancer proliferation in tissue culture is tonically inhibited by opioid growth factor
G J Bisignani1, P J McLaughlin, S D Ordille
1Department of Surgery, The Pennsylvania State University College of Medicine, Hershey 17033, USA.
Purpose:
Peptide growth factors alter cellular events by binding to specific receptors. One group of peptides, the endogenous opioids, is important in the growth of normal and neoplastic tissue. [Met5]enkephalin, also termed opioid growth factor (OGF), is a tonically active inhibitory factor that interacts with the OGF receptor, OGFr, formerly identified as Greek zeta (zeta) and appears to be autocrine produced by human cancer cells. This study examined the hypothesis that OGF directly inhibits proliferation of renal cell carcinoma in tissue culture.
Materials And Methods:
Human renal cancer cells (Caki-2) were grown using routine tissue culture techniques. A variety of natural and synthetic opioids including OGF, opioid antagonists, and opioid antibodies were added to renal cancer cell cultures to determine role of these peptides in renal cell carcinoma. The experiments were repeated in serum-free media, and with 4 other human renal cancer cell lines: Caki-2, A498, SN12C, and ACHN. Immunocytochemistry was performed to examine the presence of OGF and its receptor.
Results:
OGF was the most potent opioid peptide to influence human renal cell carcinoma. OGF depressed growth within 12 hours of treatment, with cell numbers subnormal by up to 48% of control levels. OGF action was receptor mediated, reversible, not cytotoxic, neutralized by antibodies to the peptide, and detected in the human renal cell carcinoma lines examined. OGF appeared to be autocrine produced and secreted, and was constitutively expressed. Both OGF and its receptor were detected in these cells.
Conclusion:
OGF tonically inhibits renal cancer cell proliferation in tissue culture, and may play a role in the pathogenesis and management of human renal cell cancer.
Insights
Opioid growth factor (OGF) significantly inhibits renal cancer cell proliferation in tissue culture. This peptide receptor-mediated effect suggests OGF plays a role in renal cell carcinoma pathogenesis and treatment.
Area of Science:
- Oncology
- Molecular Biology
- Endocrinology
Background:
- Peptide growth factors regulate cellular events via specific receptors.
- Endogenous opioids, including [Met5]enkephalin (opioid growth factor, OGF), are implicated in normal and neoplastic tissue growth.
- OGF interacts with its receptor (OGFr) and is autocrine-produced by human cancer cells.
Purpose of the Study:
- To investigate the hypothesis that OGF directly inhibits the proliferation of renal cell carcinoma (RCC) in vitro.
- To elucidate the role of OGF and its receptor in RCC cell growth.
Main Methods:
- Human RCC cell lines (Caki-2, A498, SN12C, ACHN) were cultured using standard techniques.
- Treatment with OGF, opioid antagonists, and antibodies was performed to assess OGF's role.
- Immunocytochemistry was utilized to detect OGF and OGFr expression within the cancer cells.
Main Results:
- OGF demonstrated potent inhibition of RCC cell growth, reducing cell numbers by up to 48% within 12 hours.
- OGF's inhibitory effect was receptor-mediated, reversible, non-cytotoxic, and neutralized by specific antibodies.
- Both OGF and its receptor (OGFr) were constitutively expressed and detected in the examined human RCC cell lines, indicating autocrine signaling.
Conclusions:
- OGF exerts tonic inhibition on renal cancer cell proliferation in tissue culture.
- These findings suggest OGF may be a significant factor in the pathogenesis and potential management of human renal cell cancer.
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