车站3
癌症研究
信号转导
STAT蛋白
计算生物学
医学
受体酪氨酸激酶
生物
生物信息学
细胞生物学
作者
Taiwo Adesoye,Debasish Tripathy,Kelly K. Hunt,Khandan Keyomarsi
出处
期刊:Cancers
[MDPI AG]
日期:2024-01-24
卷期号:16 (3): 492-492
被引量:5
标识
DOI:10.3390/cancers16030492
摘要
Signal Transducer and Activator of Transcription 3 (STAT3) plays a significant role in diverse physiologic processes, including cell proliferation, differentiation, angiogenesis, and survival. STAT3 activation via phosphorylation of tyrosine and serine residues is a complex and tightly regulated process initiated by upstream signaling pathways with ligand binding to receptor and non-receptor-linked kinases. Through downstream deregulation of target genes, aberrations in STAT3 activation are implicated in tumorigenesis, metastasis, and recurrence in multiple cancers. While there have been extensive efforts to develop direct and indirect STAT3 inhibitors using novel drugs as a therapeutic strategy, direct clinical application remains in evolution. In this review, we outline the mechanisms of STAT3 activation, the resulting downstream effects in physiologic and malignant settings, and therapeutic strategies for targeting STAT3. We also summarize the pre-clinical and clinical evidence of novel drug therapies targeting STAT3 and discuss the challenges of establishing their therapeutic efficacy in the current clinical landscape.
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