Cheng Li, Guo Mingyue, Farooqi Ammad Ahmad, Wang Linlin, Zhang Yuxi, Ye Hanlin, Qiao Gan, Lin Xiukun
Drug Clinical Trial Institution Office, Suining Central Hospital, Suining, 629000, Sichuan, China.
Department of Pharmacology, Southwest Medical University, Luzhou, 646000, Sichuan, China.
Discov Oncol. 2025 Jun 12;16(1):1069. doi: 10.1007/s12672-025-02786-8.
Maslinic acid (MA), a pentacyclic triterpenoid, displays broad biological activity including anti-inflammatory, antihyperlipidemic, anti-tumor, cardiovascular protection etc. Our previous study has shown that MA inhibits the proliferation of pancreatic cancer cells via heat shock protein HSPA8-mediated autophagy pathway, but the detailed mechanism is still unclear. In the present study, we confirmed that MA downregulated the protein expression of the transcription factor of heat shock protein 1(HSF1), and knockdown of HSF1 was able to enhance the inhibitory effect of MA in pancreatic cancer cells. In contrast, high HSF1 expression was capable of partially reversing the MA-induced inhibitory effect and the ability of MA-induced autophagy in pancreatic cancer cells. Real-time quantitative PCR and Western blotting analysis indicated that MA reduced the protein expression of HSF1 but did not downregulate mRNA levels. Molecular docking and SPR analysis revealed that there was an specific interaction between MA and HSF1; MA was able to form hydrogen bonds with the amino acid residues, HIS-63 and GLN-72 on HSF1 molecules. Co-immunoprecipitation experiments confirmed that MA promoted the ubiquitination-mediated degradation of HSF1. Further study confirmed that the mutant of His-63 and Gln-72 amino acid residues of HSF1 partially reversed the inhibitory effect of MA on the autophagy and the growth of pancreatic cancer cells. Our study provides solid evidence that there is a specific interaction between MA and HSF1, and the interaction increases the ubiquitination-mediated degradation of HSF1, contributing to the inhibitory effect of pancreatic cancer cell growth. The study also suggests that targeting the binding sites of MA on HSF1 could be developed as a novel strategy for developing anticancer agents on the treatment of pancreatic cancer.
齐墩果酸(MA)是一种五环三萜类化合物,具有广泛的生物学活性,包括抗炎、抗高血脂、抗肿瘤、心血管保护等。我们之前的研究表明,MA通过热休克蛋白HSPA8介导的自噬途径抑制胰腺癌细胞的增殖,但其详细机制仍不清楚。在本研究中,我们证实MA下调了热休克蛋白1(HSF1)转录因子的蛋白表达,敲低HSF1能够增强MA对胰腺癌细胞的抑制作用。相反,高HSF1表达能够部分逆转MA诱导的抑制作用以及MA诱导胰腺癌细胞自噬的能力。实时定量PCR和蛋白质印迹分析表明,MA降低了HSF1的蛋白表达,但未下调mRNA水平。分子对接和表面等离子体共振分析表明,MA与HSF1之间存在特异性相互作用;MA能够与HSF1分子上的氨基酸残基HIS-63和GLN-72形成氢键。免疫共沉淀实验证实,MA促进了HSF1的泛素化介导的降解。进一步研究证实,HSF1的His-63和Gln-72氨基酸残基突变体部分逆转了MA对自噬和胰腺癌细胞生长的抑制作用。我们的研究提供了确凿的证据,证明MA与HSF1之间存在特异性相互作用,这种相互作用增加了HSF1的泛素化介导的降解,有助于抑制胰腺癌细胞的生长。该研究还表明,靶向MA在HSF1上的结合位点可能被开发为一种治疗胰腺癌的新型抗癌药物策略。