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Increased expression of SSEA-4 on TKI-resistant non-small cell lung cancer with EGFR-T790M mutation.
Chen, Nai-Yu; Lin, Chih-Wei; Lai, Ting-Yen; Wu, Chung-Yi; Liao, Pei-Chi; Hsu, Tsui-Ling; Wong, Chi-Huey.
Afiliação
  • Chen NY; Genomics Research Center, Academia Sinica, Taipei 11529, Taiwan.
  • Lin CW; Institute of Microbiology and Immunology, National Yang-Ming University, Taipei 11221, Taiwan.
  • Lai TY; Institute of Biochemistry and Molecular Biology, China Medical University, Taichung 406040, Taiwan.
  • Wu CY; Graduate Institute of Biomedical Sciences, China Medical University, Taichung 406040, Taiwan.
  • Liao PC; Genomics Research Center, Academia Sinica, Taipei 11529, Taiwan.
  • Hsu TL; Genomics Research Center, Academia Sinica, Taipei 11529, Taiwan.
  • Wong CH; Institute of Biochemistry and Molecular Biology, China Medical University, Taichung 406040, Taiwan.
Proc Natl Acad Sci U S A ; 121(5): e2313397121, 2024 Jan 30.
Article em En | MEDLINE | ID: mdl-38252815
ABSTRACT
Non-small cell lung cancer (NSCLC), a major life-threatening disease accounting for 85% of all lung cancer cases, has been treated with tyrosine kinase inhibitors (TKIs), but often resulted in drug resistance, and approximately 60% of TKI-resistant cases are due to acquired secondary (epithelial growth factor receptor) EGFR-T790M mutation. To identify alternative targets for TKI-resistant NSCLC with EGFR-T790M mutation, we found that the three globo-series glycosphingolipids are increasingly expressed on this type of NSCLC cell lines, and among them, the increase of stage-specific embryonic antigen-4 (SSEA-4) expression is the most significant. Compared to TKI-sensitive cell lines, SSEA-4 and the key enzyme ß3GalT5 responsible for the synthesis of SSEA3 are more expressed in TKI-resistant NSCLC cell lines with EGFR-T790M mutation, and the expression levels strongly correlate with poor survival in patients with EGFR mutation. In addition, we demonstrated that a SSEA-4 targeted monoclonal antibody, especially the homogeneous glycoform with well-defined Fc glycan designed to improve effective functions, is highly effective against this subpopulation of NSCLC in cell-based and animal studies. These findings provide a direction for the prediction of tumor recurrence and treatment of TKI-resistant NSCLC with EGFR-T790M mutation.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Carcinoma Pulmonar de Células não Pequenas / Antígenos Embrionários Estágio-Específicos / Neoplasias Pulmonares Tipo de estudo: Prognostic_studies Limite: Animals / Humans Idioma: En Revista: Proc Natl Acad Sci U S A Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Taiwan

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Carcinoma Pulmonar de Células não Pequenas / Antígenos Embrionários Estágio-Específicos / Neoplasias Pulmonares Tipo de estudo: Prognostic_studies Limite: Animals / Humans Idioma: En Revista: Proc Natl Acad Sci U S A Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Taiwan