Hao Zhenzhen, Zhao Bo, An Fei, Zhang Wanting, Zhu Xiaoshuang, Meng Shihao, Wang Bing
Institute of Biochemistry and Molecular Biology, College of Life and Health Sciences, Northeastern University, Shenyang 110819, China.
Int J Mol Sci. 2025 Apr 10;26(8):3576. doi: 10.3390/ijms26083576.
The enhancement of stemness in cancer cells is correlated with the malignancy level in human cancers. B cell receptor-associated protein 31 (BAP31) has been implicated in tumor progression; however, its specific role in breast cancer remains unclear. This study aimed to elucidate the biological function and molecular mechanisms of BAP31 in tumorigenesis and cancer stemness. Cancer stemness was assessed through tumor sphere formation and flow cytometry assays. Western blot analysis was employed to examine alterations in core stemness factors in BAP31 knockdown cell lines, in order to explore potential underlying mechanisms. Finally, we explored the role of BAP31 by developing xenograft models using nude mice in vivo. Our findings revealed that BAP31 expression was elevated in breast cancer cells, and its knockdown led to a decrease in both sphere formation and the CD44+CD24- population. Furthermore, the knockdown of BAP31 significantly diminished the expression of core stemness factors, such as Sox2 and c-Myc, in breast cancer cells in vitro. Consistently, the suppression of BAP31 markedly inhibited the tumorigenicity and stemness of breast cancer in vivo. The functional analysis further indicated that the knockdown of BAP31 diminishes stemness by activating the Hippo pathway kinase MST1 and inhibiting the transcription factor YAP. Notably, our study was the first to demonstrate that BAP31 interacts with PCMT1, a direct negative regulator of MST1 kinase. These findings identify BAP31 as a regulator of the Hippo pathway, highlighting its critical role in breast cancer tumorigenesis and stemness. Consequently, BAP31 emerges as a potential therapeutic target for this malignancy.
癌细胞干性的增强与人类癌症的恶性程度相关。B细胞受体相关蛋白31(BAP31)与肿瘤进展有关;然而,其在乳腺癌中的具体作用仍不清楚。本研究旨在阐明BAP31在肿瘤发生和癌症干性中的生物学功能及分子机制。通过肿瘤球形成和流式细胞术检测评估癌症干性。采用蛋白质免疫印迹分析来检测BAP31基因敲低细胞系中核心干性因子的变化,以探索潜在的机制。最后,我们通过在裸鼠体内建立异种移植模型来探究BAP31的作用。我们的研究结果显示,BAP31在乳腺癌细胞中的表达升高,其基因敲低导致球体形成减少以及CD44+CD24-细胞群减少。此外,在体外,BAP31基因敲低显著降低了乳腺癌细胞中核心干性因子如Sox2和c-Myc的表达。同样,抑制BAP31在体内显著抑制了乳腺癌的致瘤性和干性。功能分析进一步表明,BAP31基因敲低通过激活Hippo通路激酶MST1并抑制转录因子YAP来降低干性。值得注意的是,我们的研究首次证明BAP31与MST1激酶的直接负调控因子PCMT1相互作用。这些发现确定BAP31为Hippo通路的调节因子,突出了其在乳腺癌肿瘤发生和干性中的关键作用。因此,BAP31成为这种恶性肿瘤的潜在治疗靶点。