mProX™ Human MAPK14 Stable Cell Line
- Product Category:
- Membrane Protein Stable Cell Lines
- Subcategory:
- Kinase Cell Lines
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Published Data
Fig.1 MAPK14 knockdown reduced the rate of cell division.
The biological function of MAPK14 in ccRCC was further investigated by conducting a cell proliferation test in MAPK14-knockdown cells. It was observed that, following transfection with MAPK14 siRNAs for 72 hours, a significant decrease in proliferation ability was noted in the cells after MAPK14 knockdown (P < .05), as indicated by the results of the EdU test.
Ref: Liu, Junlong, et al. "Knockdown of MAPK14 inhibits the proliferation and migration of clear cell renal cell carcinoma by downregulating the expression of CDC25B." Cancer Medicine 9.3 (2020): 1183-1195.
Pubmed: 31856414
DOI: 10.1002/cam4.2795
Research Highlights
Xia, Yong. et al. "Proteomics, Transcriptomics, and Phosphoproteomics Reveal the Mechanism of Talaroconvolutin-A Suppressing Bladder Cancer via Blocking Cell Cycle and Triggering Ferroptosis." Molecular & cellular proteomics : MCP, 2023.
TalaA, a compound sourced from the endophytic fungus T. convolutispora within the Chinese herbal medicine Panax notoginseng, holds promise as a potential bladder cancer treatment. Through a series of in vitro experiments, including CCK8 assays, EdU staining, crystal violet staining, flow cytometry, living/dead cell staining, and Western blotting, researchers explored its anticancer properties. Additionally, xenograft tumor implantation studies were conducted, assessing antitumor effects via H&E and immunohistochemistry staining. Proteomics, transcriptomics, and phosphoproteomics revealed TalaA's influence on cell proliferation, DNA replication, and colony formation, indicating its potential as a bladder cancer therapy targeting MAPKs, cell cycle regulation, and ferroptosis induction.
Xia, Yong. et al. "Proteomics, Transcriptomics, and Phosphoproteomics Reveal the Mechanism of Talaroconvolutin-A Suppressing Bladder Cancer via Blocking Cell Cycle and Triggering Ferroptosis." Molecular & cellular proteomics : MCP, 2023.
Pubmed:
37866481
DOI:
10.1016/j.mcpro.2023.100672
Wang, ChunPeng. et al. "Network pharmacology-based strategy to investigate the effect and mechanism of α-solanine against glioma." BMC complementary medicine and therapies, 2023.
In this study, α-solanine, a bioactive compound derived from the Chinese herb Solanum nigrum L., was examined for its potential anti-glioma properties and underlying mechanisms. Using network pharmacology, molecular docking, and molecular biology experiments, researchers predicted α-solanine's targets and identified common targets with glioma-related genes. They pinpointed 11 hub genes and explored associated signaling pathways, such as MAP kinase activity and PI3K-Akt. Furthermore, α-solanine demonstrated the ability to hinder glioma cell proliferation and migration while promoting apoptosis. The study suggested STAT1 as a potential mediator of α-solanine's impact on glioma prognosis, paving the way for novel anti-glioma treatments.
Wang, ChunPeng. et al. "Network pharmacology-based strategy to investigate the effect and mechanism of α-solanine against glioma." BMC complementary medicine and therapies, 2023.
Pubmed:
37865727
DOI:
10.1186/s12906-023-04215-1