ATAD2 is a potential immunotherapy target for patients with small cell lung cancer harboring HLA-A0201

Li Yuan1, Sini Li2, Yixiang Zhu1

  • 1State Key Laboratory of Molecular Oncology, CAMS Key Laboratory of Translational Research on Lung Cancer, Department of Medical Oncology, National Cancer Centre/National Clinical Research Centre for Cancer/Cancer Hospital, Chinese Academy of Medical Sciences Peking Union Medical College, Beijing, 100021, China.

Ebiomedicine
|January 14, 2025
PubMed
Abstract

Insights

This study identifies the ATAD2 YSDDDVPSV immunopeptide as a promising target for small cell lung cancer (SCLC) immunotherapy. This discovery offers a new strategy for developing adoptive T cell therapies for SCLC patients.

Area of Science:

  • Oncology
  • Immunology
  • Biochemistry

Background:

  • Small cell lung cancer (SCLC) is an aggressive neuroendocrine tumor with poor prognosis.
  • Effective immune-based therapies for SCLC are limited by the lack of identified tumor antigens.

Purpose of the Study:

  • To identify novel tumor antigens for SCLC immunotherapy.
  • To investigate the expression and potential of ATPase family AAA domain-containing protein 2 (ATAD2) as a therapeutic target.

Main Methods:

  • Liquid chromatography-tandem mass spectrometry (LC-MS/MS) was used to analyze cancer/testis antigens (CTAs) in SCLC.
  • Immunohistochemistry and RNA sequencing were employed to assess ATAD2 expression in SCLC and other lung cancers.
  • Immunopeptidomics identified specific ATAD2-derived epitopes for T cell recognition.

Main Results:

  • ATAD2 was significantly overexpressed in SCLC compared to normal tissues and non-small cell lung cancer (NSCLC).
  • The ATAD2-derived peptide YSDDDVPSV (HLA-A*02:01 restricted) was identified as a promising tumor antigen.
  • HLA-A*02:01 T cells showed a robust response to the YSDDDVPSV immunopeptide.

Conclusions:

  • The ATAD2 YSDDDVPSV immunopeptide represents a potential target for SCLC immunotherapy.
  • This finding supports the development of adoptive T cell therapies for ASCL1-positive or NEUROD1-positive SCLC with HLA-A*02:01.

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