核转染
妊娠期
TSG101型
反射减退
关节软骨损伤
蛋白质基因组学
液化
渗滤
食欲不振
借口
易熔合金
三醋酸甘油酯
心包积血
降职
肾小管病变
作者
Huanyan Peng,Man Liu,S. Liu,Chun Ning,Dongye Yang
标识
DOI:10.1080/17520363.2025.2521254
摘要
Sulf-2, a key member of the sulfatase family, regulated tumor progression, invasion, and metastasis through various mechanisms including genetic alterations, epigenetic modifications, transcriptional regulation, and microenvironmental influences. The dysregulation of Sulf-2 has been implicated as a pivotal driver in the development of numerous tumors. The lack of a comprehensive understanding of Sulf-2 enzymatic activities has limited the advancement of research progress, largely due to the intricate modulation of heparan sulfate (HS) biology by this enzyme. In this review, we will comprehensively discuss the structure, function, and regulatory mechanisms of Sulf-2, elucidated the mechanisms of Sulf-2 in different human-type tumors. Furthermore, we would summarize the potential applications and limitations of Sulf-2 as a target in combining therapies for human tumors, providing insights that could be instrumental in advancing targeted cancer treatments. Our comprehensive review will shed light on the multifaceted role and therapeutic potential of Sulf-2 in human tumor biology.
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