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Curr Pathobiol Rep. 2013 Dec 01;1(4):239-245. doi: 10.1007/s40139-013-0032-9.

Autophagy Modulation in Disease Therapy: Where Do We Stand?.

Current pathobiology reports

Michael P Nelson, John J Shacka

Affiliations

  1. Department of Pathology, Neuropathology Division, University of Alabama at Birmingham, Sparks Clinics Room SC 930B, 1720 7 Ave S., Birmingham, AL 35294, USA.
  2. Department of Pathology, Neuropathology Division, University of Alabama at Birmingham, Birmingham VA Medical Center, Sparks Clinics Room SC 930B, 1720 7 Ave S., Birmingham, AL 35294, USA.

PMID: 24470989 PMCID: PMC3901121 DOI: 10.1007/s40139-013-0032-9

Abstract

Since it was first described more than 50 years ago autophagy has been examined in many contexts, from cell survival to pathogen sequestration and removal. In more recent years our understanding of autophagy has developed sufficiently to allow effective targeted therapeutics to be developed against various diseases. The field of autophagy research is expanding rapidly, demonstrated by increases in both numbers of investigators in the field and the breadth of topics being addressed. Some diseases, such as the many cancers, have come to the fore in autophagy therapeutics research as a better understanding of their underlying mechanisms has surfaced. Numerous treatments are being developed and explored, from creative applications of the classic autophagy modulators chloroquine and rapamycin, to repurposing drugs approved for other treatments, such as astemizole, which is currently in use as an antimalarial and chronic rhinitis treatment. The landscape of autophagy modulation in disease therapy is rapidly changing and this review hopes to provide a cross-section of the current state of the field.

Keywords: Alzheimer's disease; Parkinson's disease; autophagy; cancer; disease treatment; ischemia; neurodegeneration; neuropathology; pathobiology; pharmacological therapy; reperfusion; stroke

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