Mimotope-hormesis and mortalin/grp75/mthsp70: A new hypothesis on how infectious disease-associated epitope mimicry may explain low cancer burden in developing nations
College
College of Science
Department/Unit
Biology
Document Type
Article
Source Title
FEBS Letters
Volume
579
Issue
3
First Page
586
Last Page
590
Publication Date
1-31-2005
Abstract
It is generally observed that countries with heavy infectious burden show lower cancer incidence as compared to more affluent nations. With the emerging paradigm on microbial heat shock proteins (hsps) as molecular link between infections and autoimmune diseases, we posit a new hypothesis, the “mimotope-hormesis”, on the immunologic impact of infections on regional cancer prevention. According to this, assaults of infection during early adulthood could fortify the immune system to evoke more potent defenses against late-onset diseases, such as cancer, via autoimmunity. Interestingly, both experimental and clinical data support the beneficial role of autoimmunity in long-term cancer survivors. We illustrate this by a comprehensive in silico mimotope (epitope mimicry) analysis of human infectious pathogens against mortalin (mthsp70/PB74/GRP75), a type of hsp70 protein involved in control of cell proliferation, immortalization and tumorigenesis.
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Recommended Citation
Deocaris, C. C., Taira, K., Kaul, S. C., & Wadhwa, R. (2005). Mimotope-hormesis and mortalin/grp75/mthsp70: A new hypothesis on how infectious disease-associated epitope mimicry may explain low cancer burden in developing nations. FEBS Letters, 579 (3), 586-590. Retrieved from https://animorepository.dlsu.edu.ph/faculty_research/5462
Disciplines
Biochemistry, Biophysics, and Structural Biology
Keywords
Heat shock proteins; Autoimmunity; Cancer
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