Overcoming Acquired Drug Resistance to Cancer Therapies through Targeted STAT3 Inhibition

Author:

Singh Sunanda1,Gomez Hector J.1,Thakkar Shreya2,Singh Samara P.3ORCID,Parihar Ashutosh S.1ORCID

Affiliation:

1. Singh Biotechnology, 1547 Fox Grape Loop, Lutz, FL 33558, USA

2. Department of Cell Biology, Microbiology and Molecular Biology, University of South Florida, Tampa, FL 33620, USA

3. Department of Surgery, Division of Surgical Oncology, University of Miami Miller School of Medicine, Miami, FL 33136, USA

Abstract

Anti-neoplastic agents for cancer treatment utilize many different mechanisms of action and, when combined, can result in potent inhibition of cancer growth. Combination therapies can result in long-term, durable remission or even cure; however, too many times, these anti-neoplastic agents lose their efficacy due to the development of acquired drug resistance (ADR). In this review, we evaluate the scientific and medical literature that elucidate STAT3-mediated mechanisms of resistance to cancer therapeutics. Herein, we have found that at least 24 different anti-neoplastic agents—standard toxic chemotherapeutic agents, targeted kinase inhibitors, anti-hormonal agents, and monoclonal antibodies—that utilize the STAT3 signaling pathway as one mechanism of developing therapeutic resistance. Targeting STAT3, in combination with existing anti-neoplastic agents, may prove to be a successful therapeutic strategy to either prevent or even overcome ADR to standard and novel cancer therapies.

Publisher

MDPI AG

Subject

Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Computer Science Applications,Spectroscopy,Molecular Biology,General Medicine,Catalysis

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