Source:http://linkedlifedata.com/resource/pubmed/id/20473330
Switch to
Predicate | Object |
---|---|
rdf:type | |
lifeskim:mentions | |
pubmed:issue |
28
|
pubmed:dateCreated |
2010-7-15
|
pubmed:abstractText |
A hallmark of cancer is the deregulation of cell-cycle machinery, ultimately facilitating aberrant proliferation that fuels tumorigenesis and disease progression. Particularly, in breast cancers, cyclin D1 has a crucial role in the development of disease. Recently, a highly specific inhibitor of CDK4/6 activity (PD-0332991) has been developed that may have efficacy in the treatment of breast cancer. To interrogate the utility of PD-0332991 in treating breast cancers, therapeutic response was evaluated on a panel of breast cancer cell lines. These analyses showed that the chronic loss of Rb is specifically associated with evolution to a CDK4/6-independent state and, ultimately, resistance to PD-0332991. However, to interrogate the functional consequence of Rb directly, knockdown experiments were performed in models that represent immortalized mammary epithelia and multiple subtypes of breast cancer. These studies showed a highly specific role for Rb in mediating the response to CDK4/6 inhibition that was dependent on transcriptional repression manifest through E2F, and the ability to attenuate CDK2 activity. Acquired resistance to PD-03322991 was specifically associated with attenuation of CDK2 inhibitors, indicating that redundancy in CDK functions represents a determinant of therapeutic failure. Despite these caveats, in specific models, PD-0332991 was a particularly effective therapy, which induced Rb-dependent cytostasis. Combined, these findings indicate the critical importance of fully understanding cell-cycle regulatory pathways in directing the utilization of CDK inhibitors in the clinic.
|
pubmed:language |
eng
|
pubmed:journal | |
pubmed:citationSubset |
IM
|
pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/6-acetyl-8-cyclopentyl-5-methyl-2-(5...,
http://linkedlifedata.com/resource/pubmed/chemical/Cyclin-Dependent Kinase 4,
http://linkedlifedata.com/resource/pubmed/chemical/Cyclin-Dependent Kinase 6,
http://linkedlifedata.com/resource/pubmed/chemical/Piperazines,
http://linkedlifedata.com/resource/pubmed/chemical/Protein Kinase Inhibitors,
http://linkedlifedata.com/resource/pubmed/chemical/Pyridines
|
pubmed:status |
MEDLINE
|
pubmed:month |
Jul
|
pubmed:issn |
1476-5594
|
pubmed:author | |
pubmed:issnType |
Electronic
|
pubmed:day |
15
|
pubmed:volume |
29
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
4018-32
|
pubmed:meshHeading |
pubmed-meshheading:20473330-Breast Neoplasms,
pubmed-meshheading:20473330-Cell Line, Tumor,
pubmed-meshheading:20473330-Cyclin-Dependent Kinase 4,
pubmed-meshheading:20473330-Cyclin-Dependent Kinase 6,
pubmed-meshheading:20473330-Female,
pubmed-meshheading:20473330-Humans,
pubmed-meshheading:20473330-Piperazines,
pubmed-meshheading:20473330-Protein Kinase Inhibitors,
pubmed-meshheading:20473330-Pyridines
|
pubmed:year |
2010
|
pubmed:articleTitle |
Therapeutic CDK4/6 inhibition in breast cancer: key mechanisms of response and failure.
|
pubmed:affiliation |
Kimmel Cancer Center, Philadelphia, PA, USA.
|
pubmed:publicationType |
Journal Article
|