Yu-Ra Choi , Mihwa Hwang , Jaemin Kim , Seog-Yun Park , Sunshin Kim , Jae J. Song , Youngjoo Lee
{"title":"极光激酶B抑制克服met扩增肺癌中met靶向耐药","authors":"Yu-Ra Choi , Mihwa Hwang , Jaemin Kim , Seog-Yun Park , Sunshin Kim , Jae J. Song , Youngjoo Lee","doi":"10.1016/j.bbamcr.2025.120001","DOIUrl":null,"url":null,"abstract":"<div><div>MET-targeted therapies are the most effective treatment for patients with <em>MET</em>-amplified lung cancer. However, acquired drug resistance is a significant challenge in <em>MET</em>-amplified lung cancer treatment. This study aimed to discover an effective treatment strategy for overcoming MET-targeted drug resistance. We first established a lung cancer cell line resistant to MET tyrosine kinase inhibitor (MET-TKI) (H1993 PR-S2) from <em>MET</em>-amplified lung cancer cells (H1993). High-throughput screening using an anti-cancer compound library identified Aurora Kinase B (AURKB) inhibitor as a potent agent suppressing H1993 PR-S2 cell viability. In these resistant cells, p-MET expression was markedly decreased, while p-AURKB was significantly increased. Furthermore, STAT3-activated gene signatures were enriched in H1993 PR-S2 cells, and p-STAT3 expression was closely linked to AURKB. The AURKB overexpression induced p-STAT3 activation in the parental cells, whereas the AURKB knockdown reduced p-STAT3 expression in the H1993 PR-S2 cells. The resistant cells showed increased BCL2 gene expression, and STAT3-BCL2 expression was highly suppressed by AURKB inhibitor. However, MET-TKI sensitivity was not enhanced by STAT3 or BCL2 knockdown in H1993 PR-S2 cells. Additionally, the elevated expression of cleavage-caspase3 and the G2/M phase arrest were observed at lower concentrations of AURKB inhibitor in the H1993 PR-S2 cells. AURKB inhibitor also showed potent anti-tumor activity against the H1993 PR-S2 tumor xenografts. Finally, we confirmed the upregulated AURKB and p-STAT3 expression in post-treatment tumors of advanced <em>MET</em>-amplified lung cancer patient who experienced acquired resistance to MET-targeted drugs. These findings suggest AURKB is a potential druggable target for MET-TKI-resistant <em>MET</em>-amplified lung cancer treatment.</div></div>","PeriodicalId":8754,"journal":{"name":"Biochimica et biophysica acta. Molecular cell research","volume":"1872 7","pages":"Article 120001"},"PeriodicalIF":3.7000,"publicationDate":"2025-06-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Overcoming MET-targeted drug resistance in MET-amplified lung cancer by aurora kinase B inhibition\",\"authors\":\"Yu-Ra Choi , Mihwa Hwang , Jaemin Kim , Seog-Yun Park , Sunshin Kim , Jae J. Song , Youngjoo Lee\",\"doi\":\"10.1016/j.bbamcr.2025.120001\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>MET-targeted therapies are the most effective treatment for patients with <em>MET</em>-amplified lung cancer. However, acquired drug resistance is a significant challenge in <em>MET</em>-amplified lung cancer treatment. This study aimed to discover an effective treatment strategy for overcoming MET-targeted drug resistance. We first established a lung cancer cell line resistant to MET tyrosine kinase inhibitor (MET-TKI) (H1993 PR-S2) from <em>MET</em>-amplified lung cancer cells (H1993). High-throughput screening using an anti-cancer compound library identified Aurora Kinase B (AURKB) inhibitor as a potent agent suppressing H1993 PR-S2 cell viability. In these resistant cells, p-MET expression was markedly decreased, while p-AURKB was significantly increased. Furthermore, STAT3-activated gene signatures were enriched in H1993 PR-S2 cells, and p-STAT3 expression was closely linked to AURKB. The AURKB overexpression induced p-STAT3 activation in the parental cells, whereas the AURKB knockdown reduced p-STAT3 expression in the H1993 PR-S2 cells. The resistant cells showed increased BCL2 gene expression, and STAT3-BCL2 expression was highly suppressed by AURKB inhibitor. However, MET-TKI sensitivity was not enhanced by STAT3 or BCL2 knockdown in H1993 PR-S2 cells. Additionally, the elevated expression of cleavage-caspase3 and the G2/M phase arrest were observed at lower concentrations of AURKB inhibitor in the H1993 PR-S2 cells. AURKB inhibitor also showed potent anti-tumor activity against the H1993 PR-S2 tumor xenografts. Finally, we confirmed the upregulated AURKB and p-STAT3 expression in post-treatment tumors of advanced <em>MET</em>-amplified lung cancer patient who experienced acquired resistance to MET-targeted drugs. These findings suggest AURKB is a potential druggable target for MET-TKI-resistant <em>MET</em>-amplified lung cancer treatment.</div></div>\",\"PeriodicalId\":8754,\"journal\":{\"name\":\"Biochimica et biophysica acta. 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Overcoming MET-targeted drug resistance in MET-amplified lung cancer by aurora kinase B inhibition
MET-targeted therapies are the most effective treatment for patients with MET-amplified lung cancer. However, acquired drug resistance is a significant challenge in MET-amplified lung cancer treatment. This study aimed to discover an effective treatment strategy for overcoming MET-targeted drug resistance. We first established a lung cancer cell line resistant to MET tyrosine kinase inhibitor (MET-TKI) (H1993 PR-S2) from MET-amplified lung cancer cells (H1993). High-throughput screening using an anti-cancer compound library identified Aurora Kinase B (AURKB) inhibitor as a potent agent suppressing H1993 PR-S2 cell viability. In these resistant cells, p-MET expression was markedly decreased, while p-AURKB was significantly increased. Furthermore, STAT3-activated gene signatures were enriched in H1993 PR-S2 cells, and p-STAT3 expression was closely linked to AURKB. The AURKB overexpression induced p-STAT3 activation in the parental cells, whereas the AURKB knockdown reduced p-STAT3 expression in the H1993 PR-S2 cells. The resistant cells showed increased BCL2 gene expression, and STAT3-BCL2 expression was highly suppressed by AURKB inhibitor. However, MET-TKI sensitivity was not enhanced by STAT3 or BCL2 knockdown in H1993 PR-S2 cells. Additionally, the elevated expression of cleavage-caspase3 and the G2/M phase arrest were observed at lower concentrations of AURKB inhibitor in the H1993 PR-S2 cells. AURKB inhibitor also showed potent anti-tumor activity against the H1993 PR-S2 tumor xenografts. Finally, we confirmed the upregulated AURKB and p-STAT3 expression in post-treatment tumors of advanced MET-amplified lung cancer patient who experienced acquired resistance to MET-targeted drugs. These findings suggest AURKB is a potential druggable target for MET-TKI-resistant MET-amplified lung cancer treatment.
期刊介绍:
BBA Molecular Cell Research focuses on understanding the mechanisms of cellular processes at the molecular level. These include aspects of cellular signaling, signal transduction, cell cycle, apoptosis, intracellular trafficking, secretory and endocytic pathways, biogenesis of cell organelles, cytoskeletal structures, cellular interactions, cell/tissue differentiation and cellular enzymology. Also included are studies at the interface between Cell Biology and Biophysics which apply for example novel imaging methods for characterizing cellular processes.