Natural medicinal compounds target signal transduction pathways to overcome ABC drug efflux transporter-mediated multidrug resistance in cancer

Drug Resist Updat. 2023 Nov:71:101004. doi: 10.1016/j.drup.2023.101004. Epub 2023 Aug 21.

Abstract

ATP-binding cassette (ABC) transporters such as ABCB1, ABCG2, and ABCC1 are the major players in drug efflux-mediated multidrug resistance (MDR), which severely affects the efficacy of chemotherapy. Several synthetic compounds block the drug transport by ABC transporters; however, they exhibit a narrow therapeutic window, and produce side effects in non-target normal tissues. Conversely, the downregulation of the expression of ABC drug transporters seems to be a promising strategy to reverse MDR in cancer cells. Several signaling pathways, such as NF-κB, STAT3, Gli, NICD, YAP/TAZ, and Nrf2 upregulate the expression of ABC drug transporters in drug-resistant cancers. Recently, natural medicinal compounds have gained importance to overcome the ABC drug-efflux pump-mediated MDR in cancer. These compounds target transcription factors and the associated signal transduction pathways, thereby downregulating the expression of ABC transporters in drug-resistant cancer cells. Several potent natural compounds have been identified as lead candidates to synergistically enhance chemotherapeutic efficacy, and a few of them are already in clinical trials. Therefore, modulation of signal transduction pathways using natural medicinal compounds for the reversal of ABC drug transporter-mediated MDR in cancer is a novel approach for improving the efficiency of the existing chemotherapeutics. In this review, we discuss the modulatory role of natural medicinal compounds on cellular signaling pathways that regulate the expression of ABC transporters in drug-resistant cancer cells.

Keywords: ABC transporters; ABCB1, ABCG2, ABCC1; Multidrug resistance; Phytochemicals; Signaling pathway; Transcription factors.

Publication types

  • Review

MeSH terms

  • ATP-Binding Cassette Transporters* / genetics
  • Drug Resistance, Multiple
  • Humans
  • NF-kappa B
  • Neoplasms* / drug therapy
  • Neoplasms* / genetics
  • Signal Transduction

Substances

  • ATP-Binding Cassette Transporters
  • NF-kappa B