Affiliations 

  • 1 Department of Biomedical Sciences, Advanced Medical and Dental Institute, Universiti Sains Malaysia, Bertam, Kepala Batas, Penang 13200, Malaysia. Electronic address: wuyanming@student.usm.my
  • 2 Department of Biomedical Sciences, Advanced Medical and Dental Institute, Universiti Sains Malaysia, Bertam, Kepala Batas, Penang 13200, Malaysia. Electronic address: saudahbadriah@student.usm.my
  • 3 Department of Neurology, School of Clinical Medicine, The First Affiliated Hospital of Yangtze University, Jingzhou, Hubei 434000, China. Electronic address: pengke202403@163.com
  • 4 Department of General Surgery, Anyang People's Hospital, Anyang, Henan 450000, China. Electronic address: linhaitingsha@163.com
  • 5 Department of Social Science, Universiti Sain Malaysia, Gelugor, Penang 11700, Malaysia. Electronic address: chenghao2238@student.usm.my
  • 6 University of Debrecen, Debrecen 4032, Hungary. Electronic address: huangxufeng@mailbox.unideb.hu
  • 7 Shanghai Jiao Tong University School of Medicine, Shanghai 200240, China. Electronic address: lzr_0108@sjtu.edu.cn
Biomed Pharmacother, 2024 Aug 28;179:117348.
PMID: 39208669 DOI: 10.1016/j.biopha.2024.117348

Abstract

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.

* Title and MeSH Headings from MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.