Overcoming osimertinib resistance in NSCLC: The role of Notch1 pathway inhibition by berberine.
3/5 보강
OpenAlex 토픽 ·
Berberine and alkaloids research
Lung Cancer Treatments and Mutations
Synthesis and Biological Activity
[BACKGROUND] Resistance acquired during treatment with third-generation EGFR-TKIs, including osimertinib, continues to pose a significant obstacle in the management of advanced non-small cell lung can
APA
Xiaozhen Jiang, Wen Xia, Jiajia Fu (2026). Overcoming osimertinib resistance in NSCLC: The role of Notch1 pathway inhibition by berberine.. Tissue & cell, 100, 103365. https://doi.org/10.1016/j.tice.2026.103365
MLA
Xiaozhen Jiang, et al.. "Overcoming osimertinib resistance in NSCLC: The role of Notch1 pathway inhibition by berberine.." Tissue & cell, vol. 100, 2026, pp. 103365.
PMID
41687187 ↗
Abstract 한글 요약
[BACKGROUND] Resistance acquired during treatment with third-generation EGFR-TKIs, including osimertinib, continues to pose a significant obstacle in the management of advanced non-small cell lung cancer (NSCLC). Dysregulation of the Notch1 signaling pathway plays a critical role in tumor development as well as therapeutic resistance. Berberine (BER), a naturally derived bioactive compound, has been reported to exert diverse antitumor effects across multiple cancer types.
[METHODS] We investigated Notch1 signaling in osimertinib-resistant NSCLC cells and assessed the effects of combined berberine and osimertinib treatment on epithelial-mesenchymal transition (EMT) and drug sensitivity.
[RESULTS] Aberrant Notch1 activation promoted EMT and contributed to osimertinib resistance. Berberine inhibited Notch1 signaling, reversed EMT in resistant cells, and restored sensitivity to osimertinib with minimal toxicity.
[CONCLUSION] Berberine overcomes osimertinib resistance by targeting the Notch1 pathway and reversing EMT, providing a novel strategy to enhance EGFR-TKI efficacy in NSCLC and supporting integration of traditional Chinese medicine with targeted therapies.
[METHODS] We investigated Notch1 signaling in osimertinib-resistant NSCLC cells and assessed the effects of combined berberine and osimertinib treatment on epithelial-mesenchymal transition (EMT) and drug sensitivity.
[RESULTS] Aberrant Notch1 activation promoted EMT and contributed to osimertinib resistance. Berberine inhibited Notch1 signaling, reversed EMT in resistant cells, and restored sensitivity to osimertinib with minimal toxicity.
[CONCLUSION] Berberine overcomes osimertinib resistance by targeting the Notch1 pathway and reversing EMT, providing a novel strategy to enhance EGFR-TKI efficacy in NSCLC and supporting integration of traditional Chinese medicine with targeted therapies.
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