HE Xinyu, FU Jiarui, LYU Wenyu, HUANG Muyang, MO Jianshan, CHENG Yaxin, XU Yulian, ZHENG Lijun, ZHANG Xiaolei, QI Lu, ZHANG Lele, ZHENG Ying, HUANG Mingqing, NI Lin, LU Jinjian. Identification of Bulbocodin D and C as novel STAT3 inhibitors and their anticancer activities in lung cancer cells [J].Chin J Nat Med, 2023, 21(11): 842-851. doi: 10.1016/S1875-5364(23)60521-7
Citation: HE Xinyu, FU Jiarui, LYU Wenyu, HUANG Muyang, MO Jianshan, CHENG Yaxin, XU Yulian, ZHENG Lijun, ZHANG Xiaolei, QI Lu, ZHANG Lele, ZHENG Ying, HUANG Mingqing, NI Lin, LU Jinjian. Identification of Bulbocodin D and C as novel STAT3 inhibitors and their anticancer activities in lung cancer cells [J].Chin J Nat Med, 2023, 21(11): 842-851. doi: 10.1016/S1875-5364(23)60521-7

Identification of Bulbocodin D and C as novel STAT3 inhibitors and their anticancer activities in lung cancer cells

  • Cancer stands as one of the predominant causes of mortality globally, necessitating ongoing efforts to develop innovative therapeutics. Historically, natural products have been foundational in the quest for anticancer agents. Bulbocodin D (BD) and Bulbocodin C (BC), two bibenzyls derived from Pleione bulbocodioides (Franch.) Rolfe, have demonstrated notable in vitro anticancer activity. In human lung cancer A549 cells, the IC50s for BD and BC were 11.63 and 11.71 μmol·L−1, respectively. BD triggered apoptosis, as evidenced by an upsurge in Annexin V-positive cells and elevated protein expression of cleaved-PARP in cancer cells. Furthermore, BD and BC markedly inhibited the migratory and invasive potentials of A549 cells. The altered genes identified through RNA-sequencing analysis were integrated into the CMap dataset, suggesting BD’s role as a potential signal transducer and activator of transcription 3 (STAT3) inhibitor. SwissDock and MOE analyses further revealed that both BD and BC exhibited a commendable binding affinity with STAT3. Additionally, a surface plasmon resonance assay confirmed the direct binding affinity between these compounds and STAT3. Notably, treatment with either BD or BC led to a significant reduction in p-STAT3 (Tyr 705) protein levels, regardless of interleukin-6 stimulation in A549 cells. In addition, the extracellular signal-regulated kinase (ERK) was activated after BD or BC treatment. An enhancement in cancer cell mortality was observed upon combined treatment of BD and U0126, the MEK1/2 inhibitor. In conclusion, BD and BC emerge as promising novel STAT3 inhibitors with potential implications in cancer therapy.
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