Perspectives on microbes as oncogenic infectious agents and implications for breast cancer

Zeena E Nackerdien1

  • 1Raymond and Beverly Sackler Laboratory of Molecular Genetics and Informatics, Rockefeller University, 1230 York Ave, New York, NY 10021-6399, USA. nackerz@mail.rockefeller.edu

Medical Hypotheses
|May 1, 2008
PubMed

Insights

Emerging research suggests infectious agents, including microbes, may play a role in chronic diseases like breast cancer. Identifying these agents could personalize cancer treatment and reduce recurrence.

Area of Science:

  • Oncology
  • Microbiology
  • Immunology

Background:

  • Cancer risk assessment traditionally focuses on noninfectious agents, genetics, and epigenetics.
  • The role of infectious agents in cancer causation has been historically limited to direct oncogene damage.
  • Recent evidence links various infections to chronic diseases, influencing immune responses and disease development.

Purpose of the Study:

  • To explore the emerging evidence for infectious agents, particularly microbes, in the etiology of various cancers.
  • To address the skepticism surrounding the role of microbes in breast cancer development.
  • To highlight the potential benefits of improved experimental designs and broader definitions of infectious causation.

Main Methods:

  • Review of emerging evidence linking acute, atypical, latent, and chronic infections to disease etiology.
  • Examination of studies in model systems implicating infectious agents in gastrointestinal, liver, and lung cancers.
  • Analysis of existing data on viral associations with breast cancer and the need for further investigation into microbial roles.

Main Results:

  • Infectious agents are increasingly recognized for their influence on immune system function and chronic disease development.
  • Evidence suggests a role for infectious agents in gastrointestinal, liver, and lung cancers.
  • While viruses are associated with breast cancer, the contribution of other microbes remains under investigation.

Conclusions:

  • Improved experimental designs and a flexible definition of infectious causation are crucial for confirming or refuting the microbe-breast cancer link.
  • Identifying specific microbes, their components, or strain variants associated with breast cancer could lead to personalized treatment strategies.
  • Harnessing microbes for immunotherapy and using probiotics to mitigate treatment side effects are potential future applications in cancer management.

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