Pabcilib is an inhibitor of cyclin dependent kinase (CDK) 4 and 6. Cyclin D1 and CDK4 / 6 are downstream of the signal pathway leading to cell proliferation. In vitro, pabcilib estrogen receptor (ER) - positive breast cancer cell lines reduce cell proliferation by blocking the progression of cells from G1 to S phase of cell cycle. Compared with each drug alone, the combined treatment of pabcilib and anti estrogen resulted in decreased phosphorylation of retinoblastoma protein (RB), decreased E2F expression and signal and prevented increased growth. In vitro treatment of ER positive breast cancer cell lines with pabcilib and anti estrogen resulted in increased cell senescence, which lasted up to 6 days after drug removal.
Synonymous: | Pabcilib |
CAS: | 571190-30-2 |
Molecular Formula: | C24H29N7O2 |
Molecular Weight: | 447.53 |
Appearance: | White to beige powder |
Storage: | Closed storage at room temperature |
Category: | Tumor drugs |