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<p>Corydaline (COR), a natural isoquinoline alkaloid, was evaluated for its anticancer potential against doxorubicin-resistant Cal27 (Dox-Cal27) oral squamous carcinoma cells. Cells treated with increasing concentrations of COR (0–5&#xa0;µM) were assessed by Annexin V/PI staining, cell-cycle profiling, migration/invasion assays, and RT-qPCR. COR induced a concentration-dependent increase in apoptosis and a pronounced G<sub>2</sub>/M phase arrest, accompanied by significant inhibition of migration and invasion. At the transcriptional level, COR downregulated the anti-apoptotic gene Bcl-2 and metastasis-associated MMP-9 and MMP-13, while upregulating pro-apoptotic and mitochondrial pathway genes (Bax, p53, caspase-3, caspase-9, and cytochrome c), indicating activation of intrinsic apoptotic signaling. Furthermore, the in vivo antitumor efficacy of COR was validated in xenograft mouse models, where COR treatment significantly inhibited tumor growth in a dose-dependent manner while exhibiting favorable tolerability. Molecular docking analysis further revealed a stable binding of COR within the active pocket of Bcl-2 (binding affinity, − 7.6&#xa0;kcal/mol), involving hydrogen bonds with Arg105 and Glu95 and hydrophobic interactions with Leu96, Phe63, and Phe112, suggesting direct inhibition of Bcl-2’s anti-apoptotic function. Collectively, these findings demonstrate that COR exerts potent pro-apoptotic and anti-metastatic effects through mitochondrial pathway activation and Bcl-2 targeting, highlighting its promise as a candidate for overcoming chemoresistance in oral cancer.</p>

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Corydaline overcomes doxorubicin resistance in oral cancer by activating the p53–Bax–caspase axis and inhibiting MMP-driven invasion: an in vitro, in vivo, and in silico study

  • 期刊论文

  • 发表日期：

    2026年5月12日

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  • Siwei Zhou,
  • Xin Fu,
  • Xu Wang

摘要

Corydaline (COR), a natural isoquinoline alkaloid, was evaluated for its anticancer potential against doxorubicin-resistant Cal27 (Dox-Cal27) oral squamous carcinoma cells. Cells treated with increasing concentrations of COR (0–5 µM) were assessed by Annexin V/PI staining, cell-cycle profiling, migration/invasion assays, and RT-qPCR. COR induced a concentration-dependent increase in apoptosis and a pronounced G2/M phase arrest, accompanied by significant inhibition of migration and invasion. At the transcriptional level, COR downregulated the anti-apoptotic gene Bcl-2 and metastasis-associated MMP-9 and MMP-13, while upregulating pro-apoptotic and mitochondrial pathway genes (Bax, p53, caspase-3, caspase-9, and cytochrome c), indicating activation of intrinsic apoptotic signaling. Furthermore, the in vivo antitumor efficacy of COR was validated in xenograft mouse models, where COR treatment significantly inhibited tumor growth in a dose-dependent manner while exhibiting favorable tolerability. Molecular docking analysis further revealed a stable binding of COR within the active pocket of Bcl-2 (binding affinity, − 7.6 kcal/mol), involving hydrogen bonds with Arg105 and Glu95 and hydrophobic interactions with Leu96, Phe63, and Phe112, suggesting direct inhibition of Bcl-2’s anti-apoptotic function. Collectively, these findings demonstrate that COR exerts potent pro-apoptotic and anti-metastatic effects through mitochondrial pathway activation and Bcl-2 targeting, highlighting its promise as a candidate for overcoming chemoresistance in oral cancer.