Thoracic Cancer (Oct 2024)

Anti‐Müllerian hormone type II receptor protein expression in non‐small cell lung cancer and the effect of AMH/AMHR2 signaling on cancer cell proliferation

  • Yoshika Koinuma,
  • Yoichiro Mitsuishi,
  • Wira Winardi,
  • Moulid Hidayat,
  • Aditya Wirawan,
  • Daisuke Hayakawa,
  • Koichiro Kanamori,
  • Naohisa Matsumoto,
  • Takuo Hayashi,
  • Naoko Shimada,
  • Ken Tajima,
  • Kazuya Takamochi,
  • Fumiyuki Takahashi,
  • Kenji Suzuki,
  • Kazuhisa Takahashi

DOI
https://doi.org/10.1111/1759-7714.15309
Journal volume & issue
Vol. 15, no. 29
pp. 2090 – 2099

Abstract

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Abstract Background Non‐small cell lung cancer (NSCLC) is the leading cause of cancer‐related deaths worldwide despite advances in cancer therapeutics. In several gynecological cancers, anti‐Müllerian hormone receptor type 2 (AMHR2) mediates AMH‐induced growth inhibition and is expressed at high levels. Furthermore, 5%–8% of NSCLCs exhibit high AMHR2 expression, suggesting that AMH may inhibit the progression of some lung cancers. However, the clinical relevance of AMHR2 expression and its role in lung cancer is not fully clarified. Methods Immunostaining was performed on 79 surgical specimens of NSCLC. The Cancer Genome Atlas RNA‐seq data for lung adenocarcinoma were analyzed, and gene ontology and gene set enrichment analyses were performed. In cellular experiments, AMHR2‐overexpressing NSCLC cell lines were established, and the role of the AMH‐AMHR2 pathway in cell proliferation with recombinant human AMH protein treatment was examined. Results A total of 13 cases (16.5%) were positive for immunostaining in lung adenocarcinoma tissues; no positive signals were detected in lung squamous carcinoma tissues. Gene expression variation analysis using The Cancer Genome Atlas data showed that the expression of genes related to the cell cycle was downregulated in the AMHR2‐high group. Cellular experiments showed that activation of the AMH‐AMHR2 pathway suppressed cell proliferation. Conclusion In lung adenocarcinoma tissues with high expression of AMHR2, activation of the AMH‐AMHR2 pathway may suppress cell proliferation.

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