SOCS3
斯达
磷酸化
JAK-STAT信号通路
细胞生物学
信号转导
细胞生长
癌症研究
细胞因子信号抑制因子
细胞因子信号抑制因子1
化学
细胞
车站3
生物
基因
生物化学
抑制器
受体酪氨酸激酶
作者
Xiaoqing Li,F.F. Peng,Ying Xu,L. R. Chen,Keng‐Hsin Lan,Feinan Hu,Long Yu,S. H. Wang,LU De-xun,X. Y. Huang,Zhijian Huang,L. L. Chen,Xiaoxiao Qin,Mei-Jing Qin
标识
DOI:10.1134/s002689332570030x
摘要
Liver cancer represents the third leading cause of cancer-related mortality globally, with hepatocellular carcinoma (HCC) accounting for the majority of cases. Despite a range of treatment options, the prognosis for advanced HCC remains poor, underscoring the need for further investigation into its pathogenic mechanisms and identification of potential therapeutic targets. Interferon γ (IFNγ) plays a crucial and multifaceted role in the occurrence and development of tumors. During tumorigenesis, alterations in miRNA expression occur, leading to subsequent changes in the expression of downstream target genes. However, the precise mechanism through which IFNγ exerts its effect via miRNA remains incompletely understood. In this study, high-throughput sequencing was employed to explore the miRNAs regulated by IFNγ in an HCC cell line. The results revealed that IFNγ regulates 17 uncharacterized miRNAs and 30 named miRNAs identified in the miRNA database. Among the miRNAs regulated by IFNγ, miR-1291 emerged as a prominent candidate. This study observed that miR-1291, along with KANSL2 mRNA and protein, is significantly upregulated in HepG2 and Huh7 cells. To investigate the role of miR-1291, HepG2 cells with both overexpression and inhibition of miR-1291 were established. High-throughput sequencing was then performed to examine the functional impact of miR-1291. The sequencing results revealed that genes regulated by miR-1291 are involved in cell cycle regulation and DNA replication. These findings were validated through qRT-PCR, cell proliferation assays, and colony formation assays, all of which confirmed that miR-1291 promotes HepG2 cell proliferation. Further analysis using a luciferase reporter assay and Western blot confirmed that SOCS3 is a direct target of miR-1291. Additionally, Western blot experiments demonstrated that miR-1291 promotes phosphorylation of the JAK/STAT signaling pathway by targeting SOCS3. These observations provide compelling evidence that IFNγ exerts its effects through the coordinated regulation of gene transcription and miRNA expression, shedding new light on the immune regulation of HCC. Furthermore, miR-1291 holds promise as a novel therapeutic target for liver cancer treatment.
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