Baltayiannis G, Baltayiannis N, Tsianos E V
First Division of Internal Medicine and Hepatogastroenterology Unit, Medical School, University of Ioannina, Ioannina, Greece.
J BUON. 2008 Apr-Jun;13(2):263-5.
The suppressors of cytokine signaling (SOCS) are inhibitors of cytokine signaling that function via the Janus kinase (JAK)/signal transducers and activators of transcription (STAT) pathway. Eight SOCS (SOCS1-SOCS7 and CIS /cytokine-inducible SH2-domain) proteins with similar structures have been identified. Cytokines bind to specifi c sites on the extracellular domains of their cognitive receptor, causing receptor dimerization. This allows the recruitment of JAKs to the receptors, which then cross-phosphorylate each other before phosphorylating the receptor on key tyrosine residues. STAT molecules bind to these phosphorylated docking sites, are in turn phosphorylated, dimerized, and enter the nucleus where they initiate transcription. Some of the genes transcribed by these factors include the SOCS genes. The SOCS proteins then act to negatively regulate activated receptor complexes by inactivating JAKs or blocking recruitment sites for STATs and also may target signaling complexes for ubiquitination and degradation. Lung cancer and hepatocellular carcinoma (HCC) are associated with abnormalities of the JAK/STAT pathway. In conclusion, determining the importance of SOCS family in health and disease will no doubt aid to the development of novel therapeutic strategies in human carcinogenesis.
细胞因子信号转导抑制因子(SOCS)是细胞因子信号转导的抑制剂,通过Janus激酶(JAK)/信号转导子和转录激活子(STAT)途径发挥作用。已鉴定出8种结构相似的SOCS蛋白(SOCS1 - SOCS7和CIS/细胞因子诱导的SH2结构域)。细胞因子与其相应受体的胞外结构域上的特定位点结合,导致受体二聚化。这使得JAKs被招募到受体上,然后JAKs相互交叉磷酸化,之后再对受体上的关键酪氨酸残基进行磷酸化。STAT分子与这些磷酸化的对接位点结合,依次被磷酸化、二聚化,并进入细胞核,在细胞核中启动转录。这些因子转录的一些基因包括SOCS基因。然后,SOCS蛋白通过使JAKs失活或阻断STATs的招募位点来对活化的受体复合物起负调控作用,并且还可能将信号复合物作为泛素化和降解的靶点。肺癌和肝细胞癌(HCC)与JAK/STAT途径的异常有关。总之,确定SOCS家族在健康和疾病中的重要性无疑将有助于人类致癌作用中新治疗策略的开发。