mProX™ Human FGFR4 Stable Cell Line
- Product Category:
- Membrane Protein Stable Cell Lines
- Subcategory:
- Kinase Cell Lines
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Published Data
Fig.1 FGFR4 expression levels in 6 HCC cell lines.
By using RT-PCR and western blot analysis to measure the FGFR4 protein and mRNA levels in six HCC cells, it was discovered that HUH7, HEP3B, and HEPG2 cells had overexpressed FGFR4.
Ref: Nam, Yunju, et al. "Anti-cancer effects of 3, 4-dihydropyrimido [4, 5-d] pyrimidin-2 (1H)-one derivatives on hepatocellular carcinoma harboring FGFR4 activation." Neoplasia 24.1 (2022): 34-49.
Pubmed: 34864570
DOI: 10.1016/j.neo.2021.11.011
Research Highlights
An FGFR4 inhibitor may be effective in treating about one-third of HCC patients whose tumors produce FGF19 in addition to FGFR4 and its coreceptor klotho β (KLB). These results represent the first instance of a treatment approach that specifically targets a subset of HCC patients.
Hagel, Margit, et al. "First selective small molecule inhibitor of FGFR4 for the treatment of hepatocellular carcinomas with an activated FGFR4 signaling pathway." Cancer discovery 5.4 (2015): 424-437.
Pubmed:
25776529
DOI:
10.1158/2159-8290.CD-14-1029
An increasing body of research suggests that FGFR4 plays a significant and distinct role in the development of tumors, their ability to resist anti-tumor therapy, and the oncogenesis of various cancer types.
Levine, Kevin M., et al. "FGFR4: A promising therapeutic target for breast cancer and other solid tumors." Pharmacology & therapeutics 214 (2020): 107590.
Pubmed:
32492514
DOI:
10.1016/j.pharmthera.2020.107590