SLC and ABC Transporters in Lung Cancer: Orchestrators of Malignancy and Therapeutic Resistance

Ping Li1,2, Minlei Dong3, Binxin Chen3

  • 1Key Laboratory of Clinical Cancer Pharmacology and Toxicology Research of Zhejiang Province, Department of Clinical Pharmacology, School of Medicine, Affiliated Hangzhou First People's Hospital, Westlake University, Hangzhou, China.

Comprehensive Physiology
|February 27, 2026
PubMed
Abstract

Insights

Solute carrier (SLC) and ATP-binding cassette (ABC) transporters drive lung cancer aggressiveness and resistance. Targeting these transporters offers new strategies to overcome drug resistance and improve patient outcomes.

Area of Science:

  • Oncology
  • Molecular Biology
  • Cancer Research

Background:

  • Lung cancer is a major cause of cancer death globally.
  • Therapy resistance significantly limits treatment effectiveness.
  • Solute carrier (SLC) and ATP-binding cassette (ABC) transporters influence lung cancer progression and treatment response.

Purpose of the Study:

  • To systematically review the roles of SLC and ABC transporters in lung cancer.
  • To elucidate their mechanisms in tumor progression and the tumor microenvironment (TME).
  • To identify potential therapeutic targets for overcoming resistance.

Main Methods:

  • Systematic review of pathophysiological roles of key transporters.
  • Emphasis on transporter functions in the TME.
  • Assessment of current knowledge and molecular mechanisms.

Main Results:

  • SLC and ABC transporters promote lung cancer aggressiveness (proliferation, invasion, metastasis).
  • They suppress cell death, sustain cancer stem cells, and modulate chemotherapy resistance.
  • Transporters mediate TME immunosuppression via crosstalk with immune and stromal cells.

Conclusions:

  • SLC and ABC transporters are critical for lung cancer malignancy and therapeutic resistance.
  • They represent actionable targets for novel therapeutic strategies.
  • Targeting these transporters may improve clinical outcomes by overcoming drug resistance.

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