mProX™ Human STK26 Stable Cell Line
- Product Category:
- Membrane Protein Stable Cell Lines
- Subcategory:
- Kinase Cell Lines
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Published Data
Fig.1 Silencing STK26 MST4) in MEF cells.
In MEFs, control shRNA transduction with a scrambled sequence was employed, resulting in the induction of apparent IκBα degradation and downstream kinase activation (IKKβ, Jnk, and Erk) along with a reduction in MST4 protein abundance upon acute LPS challenge. Nevertheless, MST4 knockdown induced by shRNA further facilitated LPS-mediated signal transduction, characterized by an intensified IκBα degradation and enhanced phosphorylation of downstream kinases (IKKβ and Erk).
Ref: Jiao, Shi, et al. "The kinase MST4 limits inflammatory responses through direct phosphorylation of the adaptor TRAF6." Nature immunology 16.3 (2015): 246-257.
Pubmed: 25642822
DOI: 10.1038/ni.3097
Research Highlights
Wan, Cheng. et al. "Identification of m6A methylation-related genes in cerebral ischaemia‒reperfusion of Breviscapus therapy based on bioinformatics methods." BMC medical genomics, 2023.
In this study, researchers investigated the effects of breviscapine on cerebral ischaemia‒reperfusion (I/R)-induced neuronal damage using transcriptome sequencing in mice. They identified 2250 differentially expressed genes (DEGs) between the OGD/R and control groups and 757 DEGs between the Therapy and OGD/R groups. Moreover, seven m6A-related DEGs were pinpointed, and four key genes (Tfcp2l1, Kcns3, Olfml2a, and Arl4d) were identified, highlighting their involvement in DNA repair, e2f targets, and the g2m checkpoint. Tfcp2l1 was found to be crucial in human embryonic stem cell pluripotency. The study also revealed a circRNA-miRNA‒mRNA network regulating Tfcp2l1. These findings offer valuable insights into breviscapine's potential for OGD/R treatment, with implications for future clinical trials.
Wan, Cheng. et al. "Identification of m6A methylation-related genes in cerebral ischaemia‒reperfusion of Breviscapus therapy based on bioinformatics methods." BMC medical genomics, 2023.
Pubmed:
37670341
DOI:
10.1186/s12920-023-01651-3
Caputo, Mara. et al. "STE20-type kinases MST3 and MST4 promote the progression of hepatocellular carcinoma: Evidence from human cell culture and expression profiling of liver biopsies." FASEB journal : official publication of the Federation of American Societies for Experimental Biology, 2023.
Hepatocellular carcinoma (HCC) is a highly deadly and rapidly spreading form of cancer. Recently, the role of nonalcoholic steatohepatitis (NASH) in promoting HCC has been recognized. This study focuses on the contribution of two protein molecules, MST3 and MST4, in the development of HCC. Through analysis of various datasets and patient samples, the researchers found a positive correlation between the expression of MST3 and MST4 and the incidence and severity of HCC. Their experiments also showed that inhibiting these proteins significantly reduced the growth and invasiveness of HCC cells. Further investigations revealed that MST3 and MST4 interact with GOLGA2 and the STRIPAK complex to activate the STAT3 signaling pathway, which plays a crucial role in HCC progression. These findings suggest that targeting MST3 and MST4 may provide a promising therapeutic approach for HCC treatment.
Caputo, Mara. et al. "STE20-type kinases MST3 and MST4 promote the progression of hepatocellular carcinoma: Evidence from human cell culture and expression profiling of liver biopsies." FASEB journal : official publication of the Federation of American Societies for Experimental Biology, 2023.
Pubmed:
37490000
DOI:
10.1096/fj.202300397RR