亚科
肝细胞癌
癌变
癌症研究
生物
卵巢癌
泛素
脱氮酶
癌症
入射(几何)
卵巢癌
转化研究
癌
肿瘤科
内科学
医学
基因
遗传学
生物技术
物理
光学
作者
Yanming Wu,Sa’udah Badriah Mohd Sani,Ke Peng,Tao Lin,Chenghao Tan,Xufeng Huang,Zhengrui Li
标识
DOI:10.1016/j.biopha.2024.117348
摘要
In cancer research, oncogenesis can be affected by modulating the deubiquitination pathway. Ubiquitination regulates proteins post-translationally in variety of physiological processes. The Otubain Subfamily includes OTUB1 (ovarian tumor-associated proteinase B1) and OTUB2(ovarian tumor-associated proteinase B2). They are deubiquitinating enzymes, which are research hotspots in tumor immunotherapy, with their implications extending across the spectrum of tumor development. Understanding their important role in tumorigenesis, includ-ing hepatocellular carcinoma (HCC) is crucial. HCC has alarming global incidence rates and mortality statistics, ranking among the top five prevalent cancers in Malaysia1. Numerous studies have consistently indicated significant expression of OTUB1 and OTUB2 in HCC cells. In addition, OTUB1 has important biological functions in cancer, suggesting its important role in tumorigenesis. However, the mechanism underlying the action of OTUB1 and OTUB2 in liver cancer remains inadequately explored. Therefore, Otubain Subfamily, as potential molecular target, holds promise for advancing HCC treatments. However, further clinical studies are required to verify its efficacy and application prospects.
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