AI Article Synopsis

  • Chemotherapy is often the last resort for advanced cancer patients when other treatments are not possible, but its success can be limited due to chemoresistance mechanisms.
  • The review analyzes data from The Cancer Genome Atlas (TCGA) to investigate how major ATP-binding cassette (ABC) proteins, which contribute to drug resistance in cancer, affect the efficacy of common chemotherapy drugs.
  • ABC proteins like MDR1, MRPs, and BCRP help cancer cells expel chemotherapy drugs, thus reducing their effectiveness and allowing tumors to thrive even during treatment.

Article Abstract

: Chemotherapy remains the only option for advanced cancer patients when other alternatives are not feasible. Nevertheless, the success rate of this type of therapy is often low due to intrinsic or acquired mechanisms of chemoresistance. Among them, drug extrusion from cancer cells through ATP-binding cassette (ABC) proteins plays an important role. ABC pumps are primary active transporters involved in the barrier and secretory functions of many healthy cells. : In this review, we have used The Cancer Genome Atlas (TCGA) database to explore the relationship between the expression of the major ABC proteins involved in cancer chemoresistance in the most common types of cancer, and the drugs used in the treatment of these tumors that are substrates of these pumps. : From unicellular organisms to humans, several ABC proteins play a major role in detoxification processes. Cancer cells exploit this ability to protect themselves from cytostatic drugs. Among the ABC pumps, MDR1, MRPs and BCRP are able to export many antitumor drugs and are expressed in several types of cancer, and further up-regulated during treatment. This event results in the enhanced ability of tumor cells to reduce intracellular drug concentrations and hence the pharmacological effect of chemotherapy.

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http://dx.doi.org/10.1080/17425255.2019.1631285DOI Listing

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