The molecular biology of prostate cancer morbidity and mortality: Accelerated death from ejaculate poisoning?

E Chou1, J W Simons

  • 1From the Johns Hopkins Oncology Center and the James Buchanan Brady Urological Institute, NIH Special Program of Research Excellence in Prostate Cancer, The Johns Hopkins Hospital, Baltimore, Maryland, USA.

Urologic Oncology
|January 14, 2011
PubMed

Insights

Prostate cancer

Area of Science:

  • Oncology
  • Molecular Biology
  • Cancer Research

Background:

  • Prostate cancer's molecular biology and host-tumor interactions causing morbidity remain poorly understood.
  • The role of prostate-specific exocrine gene products in advanced prostate cancer symptoms like bone pain and cachexia is unclear.

Purpose of the Study:

  • To explore the poorly understood molecular mechanisms of host-tumor interactions in prostate cancer.
  • To investigate the role of prostate-specific exocrine gene products in mediating cancer morbidity.

Main Methods:

  • Literature review and hypothesis discussion.
  • Analysis of existing evidence on androgen-regulated exocrine gene products.

Main Results:

  • Growing evidence suggests androgen-regulated exocrine gene products may independently drive prostate cancer morbidity.
  • Prostate-specific exocrine genes are implicated in symptoms of advanced disease.

Conclusions:

  • Prostate-specific exocrine genes are hypothesized to be key mediators of prostate cancer patient morbidity.
  • Understanding these genes has significant experimental and clinical implications for managing advanced prostate cancer.

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