Cui Ao, Yu Ying-Xue, Xiong Mei-Xue, Wang Ji-Yang, Zou Ye-Qing, Zhu Ya-Qiong, Ran Long-Jian, Zhang Yu, Liu Rui-Xiang, Dong Ming-Yi, Wang Hui, Fang Lu, Fu Xiao-Wei
Department of General Surgery, The Second Affiliated Hospital of Nanchang University, Nanchang, China.
Jiangxi Province Key Laboratory of Molecular Medicine, Nanchang, China.
J Cell Mol Med. 2025 Aug;29(16):e70767. doi: 10.1111/jcmm.70767.
Pancreatic cancer (PC) is a highly lethal tumour of the gastrointestinal tract. New molecular targets are urgently needed for its treatment. Kinesin family member C1 (KIFC1) is implicated in the development and progression of several types of cancer. Previous studies from our group demonstrated that KIFC1 overexpression in hepatocellular carcinoma promotes malignant behaviours via the PI3K/AKT pathway. However, the molecular and functional mechanisms of KIFC1 in PC are not yet fully elaborated. In this study, KIFC1 and BUB1B were significantly upregulated in PC patient samples, and high KIFC1 expression was closely associated with the malignant phenotype and poorer overall survival (OS) in PC patients. Functional experiments showed that KIFC1 knockdown inhibited PC cell growth in vivo and in vitro, blocked cell cycle progression and hindered cell migration and invasion. In addition, rescue experiments showed that KIFC1 induced PC cell malignant behaviours dependent on BUB1B. Mechanistically, KIFC1 regulates BUB1B expression by competitively binding to BUB1B and reducing its ubiquitination and degradation. We have shown for the first time the molecular regulatory mechanism between KIFC1 and BUB1B on PC. Therefore, KIFC1 shows promise as an attractive therapeutic target for PC in the future.
胰腺癌(PC)是一种胃肠道高致死性肿瘤。其治疗迫切需要新的分子靶点。驱动蛋白家族成员C1(KIFC1)与多种癌症的发生和发展有关。我们团队之前的研究表明,肝细胞癌中KIFC1的过表达通过PI3K/AKT途径促进恶性行为。然而,KIFC1在胰腺癌中的分子和功能机制尚未完全阐明。在本研究中,KIFC1和BUB1B在胰腺癌患者样本中显著上调,且KIFC1高表达与胰腺癌患者的恶性表型及较差的总生存期(OS)密切相关。功能实验表明,敲低KIFC1可在体内和体外抑制胰腺癌细胞生长,阻断细胞周期进程,阻碍细胞迁移和侵袭。此外,挽救实验表明,KIFC1诱导胰腺癌细胞的恶性行为依赖于BUB1B。机制上,KIFC1通过竞争性结合BUB1B并减少其泛素化和降解来调节BUB1B的表达。我们首次揭示了KIFC1和BUB1B在胰腺癌中的分子调控机制。因此,KIFC1有望成为未来胰腺癌有吸引力的治疗靶点。