Zhang Jian, Liu Shu-Qiang, Xiong Xiang-Yu, Zhou Ya-Qing, Wei Pan-Pan, Guan Xin-Yuan, Bei Jin-Xin, Luo Chun-Ling, Cui Qian
The Eighth Affiliated Hospital, Sun Yat-sen University, Shenzhen, China.
State Key Laboratory of Oncology in South China, Guangdong Key Laboratory of Nasopharyngeal Carcinoma Diagnosis and Therapy, Guangdong Provincial Clinical Research Center for Cancer, Collaborative Innovation Center for Cancer Medicine, Sun Yat-sen University Cancer Center, Guangzhou, China.
Cell Death Dis. 2025 Jun 23;16(1):464. doi: 10.1038/s41419-025-07635-8.
CLPTM1L has been identified as a susceptibility gene associated with nasopharyngeal carcinoma (NPC) risk, but its biological function and underlying mechanisms remain unclear. Here, we demonstrate that CLPTM1L is highly expressed in NPC patients and is associated with poor prognosis. Functional assays reveal that CLPTM1L overexpression significantly enhances NPC cell proliferation, migration and invasion, whereas its knockdown induces apoptosis and suppresses tumor growth. We further uncover that the transcription factor KLF1 directly binds to the promoter of CLPTM1L, driving its transcriptional activation. Transcriptome analysis indicates that CLPTM1L regulates various lipid metabolic pathways, notably upregulating SREBP1, a key metabolic regulator, thereby increasing intracellular free fatty acid levels in NPC cells. Mechanically, CLPTM1L interacts with the lipid raft-associated protein ERLIN2 to cooperatively stabilize SREBP1 protein levels by inhibiting its ubiquitination. Furthermore, knockdown of either ERLIN2 or SREBP1 remarkably inhibits the proliferation and migration capabilities of NPC cells, synergizing with CLPTM1L depletion. Importantly, SREBP1 overexpression markedly restored the inhibitory effects mediated by CLPTM1L and ERLIN2 knockdown, underscoring SREBP1 as a critical mediator in CLPTM1L's oncogenic role. These findings delineate a novel pathogenic mechanism in NPC, highlighting the KLF1/CLPTM1L/ERLIN2/SREBP1 regulatory cascade as a promising therapeutic target for NPC treatment.
CLPTM1L已被确定为与鼻咽癌(NPC)风险相关的易感基因,但其生物学功能和潜在机制仍不清楚。在此,我们证明CLPTM1L在NPC患者中高表达,并与不良预后相关。功能试验表明,CLPTM1L过表达显著增强NPC细胞的增殖、迁移和侵袭能力,而其敲低则诱导细胞凋亡并抑制肿瘤生长。我们进一步发现转录因子KLF1直接结合CLPTM1L的启动子,驱动其转录激活。转录组分析表明,CLPTM1L调节多种脂质代谢途径,特别是上调关键代谢调节因子SREBP1,从而增加NPC细胞内游离脂肪酸水平。机制上,CLPTM1L与脂筏相关蛋白ERLIN2相互作用,通过抑制SREBP1的泛素化来协同稳定其蛋白水平。此外,敲低ERLIN2或SREBP1均可显著抑制NPC细胞的增殖和迁移能力,与CLPTM1L缺失协同作用。重要的是,SREBP1过表达显著恢复了CLPTM1L和ERLIN2敲低介导的抑制作用,强调SREBP1是CLPTM1L致癌作用的关键介质。这些发现描绘了NPC中的一种新的致病机制,突出了KLF1/CLPTM1L/ERLIN2/SREBP1调节级联作为NPC治疗的一个有前景的治疗靶点。