Published January 2018 | Version v1
Journal article

Targeting ALDH2 with disulfiram/copper reverses the resistance of cancer cells to microtubule inhibitors

  • 1. Benxi Institute of Pharmaceutical Research, Shenyang Pharmaceutical University, Shenyang (China)
  • 2. Department of Pharmacology, Shenyang Pharmaceutical University, Shenyang (China)
  • 3. Key Laboratory of Medicinal Chemical Biology, College of Pharmacy, Nankai University (China)

Description

Highlights: • DSF/Cu reversed the microtubule inhibitor resistance in cancer cells. • DSF/Cu abolished the CSC characteristics of microtubule inhibitor resistant cancer cells. • ALDH2 played a crucial role in the development of microtubule inhibitor resistance. • DSF/Cu reduced ALDH2 expression in vitro and in vivo. Disulfiram (DSF) in combination with copper (Cu) has been reported to override drug resistance in cancer cells, and DSF combined with chemotherapy based on the microtubule inhibitor vinorelbine appears to prolong survival in non-small cell lung cancer patients. Here, we investigated the mechanisms underlying these findings. DSF/Cu reversed the microtubule inhibitor resistance in A549/Taxol and KB/VCR cells in vitro, and had anti-tumor effects in A549/Taxol and KB/VCR xenograft mice. DSF/Cu and DSF reduced the cancer stem cell (CSC) characteristics of drug-resistant A549/Taxol and KB/VCR cells, including sphere formation, colony generation and migration, and DSF/Cu was more effective than DSF alone. DSF/Cu also decreased the aldehyde dehydrogenase (ALDH) activity and the expression of P-gp and stem cell transcription factors in A549/Taxol and KB/VCR cells. Knockdown of ALDH2 attenuated the CSC characteristics of resistant cancer cells and enhanced their sensitivity to Taxol or VCR. Importantly, DSF/Cu treatment inhibited the expression of ALDH2 in vitro and in vivo. Our findings suggest that DSF/Cu reverses microtubule inhibitor resistance in cancer cells by suppressing ALDH2 expression, and Cu improves the activity of DSF.

Availability note (English)

Available from http://dx.doi.org/10.1016/j.yexcr.2017.11.004

Additional details

Identifiers

DOI
10.1016/j.yexcr.2017.11.004;
PII
S0014482717306006;

Publishing Information

Journal Title
Experimental Cell Research
Journal Volume
362
Journal Issue
1
Journal Page Range
p. 72-82
ISSN
0014-4827
CODEN
ECREAL

INIS

Country of Publication
United States
Country of Input or Organization
International Atomic Energy Agency (IAEA)
INIS RN
52123271
Subject category
S60: APPLIED LIFE SCIENCES;
Descriptors DEI
CHEMOTHERAPY; COPPER; LUNGS; MICE; MICROTUBULES; NEOPLASMS; OXIDOREDUCTASES; STEM CELLS
Descriptors DEC
ANIMAL CELLS; ANIMALS; BODY; CELL CONSTITUENTS; DISEASES; ELEMENTS; ENZYMES; MAMMALS; MEDICINE; METALS; ORGANIC COMPOUNDS; ORGANS; PROTEINS; RESPIRATORY SYSTEM; RODENTS; SOMATIC CELLS; THERAPY; TRANSITION ELEMENTS; VERTEBRATES

Optional Information

Copyright
Copyright (c) 2017 Published by Elsevier Inc.