Targeting TIM-3 to halt lung precancer progression

Kostas A Papavassiliou1, Alice G Vassiliou2, Athanasios G Papavassiliou3

  • 1First University Department of Respiratory Medicine, 'Sotiria' Chest Hospital, Medical School, National and Kapodistrian University of Athens, Athens 11527, Greece.

Trends in Cancer
|July 17, 2025
PubMed

Insights

Researchers studied lung adenocarcinoma precursors and found T cell immunoglobulin and mucin domain 3 (TIM-3) may be a target. Blocking TIM-3 in mice delayed precancer progression, showing potential for high-risk individuals.

Area of Science:

  • Oncology
  • Immunology
  • Preclinical Research

Background:

  • Lung adenocarcinoma (LUAD) precancer progression remains poorly understood.
  • Early immune responses in LUAD precursors are critical for understanding disease development.

Purpose of the Study:

  • To investigate the early immunologic landscape of lung adenocarcinoma (LUAD) precursors.
  • To identify potential immune checkpoint targets for precancer interception in LUAD.

Main Methods:

  • Exploration of the immunologic microenvironment in LUAD precursors.
  • In vivo studies involving TIM-3 blockade in mice with premalignant lung lesions.

Main Results:

  • T cell immunoglobulin and mucin domain 3 (TIM-3) was identified as a potential immune checkpoint target.
  • TIM-3 blockade significantly delayed the progression from premalignant lesions to invasive adenocarcinoma in a mouse model.

Conclusions:

  • TIM-3 represents a promising therapeutic target for intercepting LUAD precancer.
  • Targeting TIM-3 may offer clinical utility for individuals at high risk for lung adenocarcinoma.