Chloroquine and hydroxychloroquine in antitumor therapies based on autophagy-related mechanisms

Pharmacol Res. 2021 Jun:168:105582. doi: 10.1016/j.phrs.2021.105582. Epub 2021 Mar 26.

Abstract

Chloroquine (CQ) and hydroxychloroquine (HCQ) are the most common drugs used to relieve acute and chronic inflammatory diseases. In this article, we present a review about the use of CQ and HCQ in antitumor therapies based on autophagy mechanisms. These molecules break/discontinue autophagosome-lysosome fusions in initial phases and enhance antiproliferative action of chemotherapeutics. Their sensitizing effects of chemotherapy when used as an adjuvant option in clinical trials against cancer. However, human related-MDR genes are also under risk to develop chemo or radioresistance because cancer cells have ability to throw 4-aminoquinolines out from digestive vacuoles well. Additionally, they also have antitumor mechanism unrelated to autophagy, including cell death from apoptosis and necroptosis and immunomodulatory/anti-inflammatory properties. However, the link between some anticancer mechanisms, clinical efficacy and pharmacological safety has not yet been fully defined.

Keywords: Cell death; Chemoresistance; Clinical option; Immunomodulatory properties.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Antineoplastic Agents / pharmacology
  • Autophagy / drug effects*
  • Chloroquine / pharmacology*
  • Chloroquine / therapeutic use
  • Clinical Trials as Topic
  • Drug Resistance, Neoplasm
  • Humans
  • Hydroxychloroquine / pharmacology*
  • Hydroxychloroquine / therapeutic use
  • Immunomodulating Agents / pharmacology
  • Neoplasms / drug therapy*

Substances

  • Antineoplastic Agents
  • Immunomodulating Agents
  • Hydroxychloroquine
  • Chloroquine