PD0332991 Isethionate

Uses

PD 0332991 isethionate has been used:

• to incubate MCF10A cells to verify cyclin D1 inhibition of autophagy involved cyclin-dependent kinase activity
• as a cyclin dependent kinase 4 (CDK4) inhibitor to study its anticonvulsive property in Drosophila
• to mimic the inhibitory effect of 5α-dihydrotestosterone (DHT) on HPr-1AR cell cycle progression and growth

Biological Activity

cyclin-dependent kinases (cdks) are a family of protein kinases first discovered for their role in regulating the cell cycle. they are also involved in regulating transcription, mrna processing, and the differentiation of nerve cells. a cyclin-dependent kinase inhibitor (cki) is a protein that interacts with a cyclin-cdk complex to block kinase activity, usually during g1 or in response to signals from the environment or from damaged dna. palbociclib is an experimental drug for the treatment of breast cancer being developed by pfizer. it is a selective inhibitor of the cyclin-dependent kinases cdk4 and cdk6.

Biochem/physiol Actions

PD 0332991 is a potent selective inhibitor of cyclin dependent kinases CDK4 and CDK6 with in vitro IC50 = 11 nM (CDK4) and 16 nM (CDK6). PD 0332991 induces G1 arrest in retinoblastoma (Rb)-positive tumor cells.

in vitro

half-maximal inhibitory concentrations (ic50) of pd-0332991 were determined with cell line proliferation assays. resutls showed that ic50 values for pd-0332991 ranged from 25.0 nm to 700 nm, and the agent demonstrated g0/g1 cell-cycle arrest, induction of late apoptosis, and blockade of rb phosphorylation. through genotype and expression data p16, p15 and e2f1 were identified as having significant association between loss and sensitivity to pd-0332991: p16 (p=0.021), p15 (p=0.047), and e2f1 (p=0.041) [1].

in vivo

oral administration of pd 0332991 to mice bearing the colo-205 human colon carcinoma produces marked tumor regression. therapeutic doses of pd 0332991 cause elimination of phospho-rb and the proliferative marker ki-67 in tumor tissue and down-regulation of genes under the transcriptional control of e2f. the results indicate that inhibition of cdk4/6 alone is sufficient to cause tumor regression and a net reduction in tumor burden in some tumors [2].

target

CDK4

IC 50

palbociclib is an orally active, potent and highly selective inhibitor of cdk4 and cdk6, with ic50 values for cdk4/cyclind1, cdk4/cyclind3 and cdk6/cyclind2 of 11, 9 and 15 nmol/l, respectively.

storage

Store at RT

References

[1] logan je, mostofizadeh n, desai aj, von euw e, conklin d, konkankit v, hamidi h, eckardt m, anderson l, chen hw, ginther c, taschereau e, bui ph, christensen jg, belldegrun as, slamon dj, kabbinavar ff. pd-0332991, a potent and selective inhibitor of cyclin-dependent kinase 4/6, demonstrates inhibition of proliferation in renal cell carcinoma at nanomolar concentrations and molecular markers predict for sensitivity. anticancer res. 2013;33(8):2997-3004.
[2] fry dw, harvey pj, keller pr, elliott wl, meade m, trachet e, albassam m, zheng x, leopold wr, pryer nk, toogood pl. specific inhibition of cyclin-dependent kinase 4/6 by pd 0332991 and associated antitumor activity in human tumor xenografts. mol cancer ther. 2004;3(11):1427-38.