The deubiquitinase USP15 drives malignant progression of gastric cancer through glucose metabolism remodeling

期刊论文
出版模式：

开放获取
发表日期：

2024年8月20日

查看全文

Longtao Huangfu,
Huanbo Zhu,
Gangjian Wang,
Junbing Chen,
Yongqi Wang,
Biao Fan,
Xiaoyang Wang,
Qian Yao,
Ting Guo,
Jing Han,
Ying Hu,
Hong Du,
Xiaomei Li,
Jiafu Ji,
Xiaofang Xing

摘要

Background

Ubiquitin-specific protease 15 (USP15) exhibits amplifications in various tumors, including gastric cancer (GC), yet its biological function and mechanisms in GC progression remain elusive.

Methods

Here, we established stable USP15 knockdown or overexpression GC cell lines and explored the potential mechanism of USP15 in GC. Besides, we also identified interacting targets of USP15.

Results

USP15 knockdown significantly impeded cell proliferation, invasion, epithelial-mesenchymal transition, and distal colonization in xenograft models, while enhancing oxaliplatin's antitumor effect. USP15 was involved in ubiquitination modification of glycolytic regulators. Silencing of USP15 suppressed glycolytic activity and impaired mitochondrial functions. Interference with USP15 expression reversed tumor progression and distal colonization in vivo. HKDC1 and IGF2BP3 were found as core interacting targets of USP15, and HKDC1 was identified as a substrate for ubiquitination modification by USP15, whereby USP15 regulated glucose metabolism activity by inhibiting the ubiquitination degradation of HKDC1.

Conclusions

Our study unveiled aberrantly high expression of USP15 in GC tissues, correlating with malignant progression and nonresponse to neoadjuvant therapy. USP15 inhibitors, if developed, could be effective in promoting chemotherapy through glucose metabolism remodeling.