mProX™ Human PTGER3 Stable Cell Line
- Product Category:
- Membrane Protein Stable Cell Lines
- Subcategory:
- GPCR Cell Lines
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Published Data
Fig.1 PTGER3 overexpression in human tumors is associated.
Real-time PCR and Western blot analyses for PTGER3 were performed on a panel of OC and normal ovarian cell lines as stated in the Methods section. The loading control used was beta-actin.
Ref: Rodriguez-Aguayo, Cristian, et al. "PTGER3 induces ovary tumorigenesis and confers resistance to cisplatin therapy through up-regulation Ras-MAPK/Erk-ETS1-ELK1/CFTR1 axis." EBioMedicine 40 (2019): 290-304.
Pubmed: 30655206
DOI: 10.1016/j.ebiom.2018.11.045
Research Highlights
For tumor-related angiogenesis, tumor development, and chemoresistance, prostaglandin E2-prostaglandin E2 receptor EP3 (PTGER3) signaling is essential. However, it is unknown what causes these effects in ovarian cancer.
Rodriguez-Aguayo, Cristian, et al. "PTGER3 induces ovary tumorigenesis and confers resistance to cisplatin therapy through up-regulation Ras-MAPK/Erk-ETS1-ELK1/CFTR1 axis." EBioMedicine 40 (2019): 290-304.
Pubmed:
30655206
DOI:
10.1016/j.ebiom.2018.11.045
This study not only revealed a portion of the molecular mechanism of CKI in GC therapy, but it also offered a cutting-edge systems pharmacology approach to investigate the mechanisms of formulations of traditional Chinese medicine.
Zhou, Wei, et al. "An advanced systems pharmacology strategy reveals AKR1B1, MMP2, PTGER3 as key genes in the competing endogenous RNA network of compound kushen injection treating gastric carcinoma by integrated bioinformatics and experimental verification." Frontiers in Cell and Developmental Biology 9 (2021): 742421.
Pubmed:
34646828
DOI:
10.3389/fcell.2021.742421