identified as a PKC inhibitor which targets the conserved ATP binding domain but the drug inhibits many other kinases. Staurosporine derivatives such Rifapentine as PKC412 and UCN01 have been developed with improved specificity and are in use in clinical trials for solid tumors and hematologic malignancies The Lilly compound enzastaurin was found to be fairly specific for PKC b and was originally developed as an anti angiogenesis agent based on the role of PKC b in that process. At higher concentrations, the drug can inhibit other PKC isoforms including PKC a. Enzastaurin has shown promise in a recent Phase II clinical trial for diffuse large B cell lymphoma. Since lung cancer cells exhibit elevated expression of both PKC a and PKC b, and enzastaurin can effectively inhibit both kinases at concentrations used in therapy, the drug is being used in clinical trials for lung cancer.
Considering that PKC plays a key role in leukemia cell survival, a strategy using enzastaurin for the therapy of AML is appealing. A recent study has shown that enzastaurin promotes death ligand induced apoptosis in leukemia cells. However, at present it is unclear how enzastaurin affects AML cells. In the present study, PKC Inhibitors we have found that PKC a and PKC b gene expression levels are significantly elevated in blast cells derived from AML patients compared to counterpart CD34þ cells Vismodegib 879085-55-9 derived from normal donors. Enzastaurin was found to be effective at promoting apoptosis in AML cell lines and leukemic blast cells from AML patients.
While suppression of PKC b does not appear to be required for enzastaurin induced cell death of the AML cells, the drug was effective buy Temozolomide at suppressing PKC a phosphorylation and membrane localization, inhibiting ERK phosphorylation, blocking BCL2 phosphorylation, and altering phosphorylation status of a distinct set of proteins. These results suggest that enzastaurin may be an effective agent in the therapy of AML.All reagents used were purchased from commercial sources unless otherwise stated. Enzastaurin was kindly provided by Eli Lilly and Company or purchased from LC Laboratories. CELL LINES AND PATIENT SAMPLES OCI AML2 and OCI AML3 cells were kindly provided by M. D. Minden. U937, KG1, K562, THP 1, and HL60 cells were obtained from the American Type Culture Collection. Cells were maintained in RPMI medium 1640 supplemented with 5% fetal bovine serum and 5% calf serum at 378C in 5%CO2.
Samples of peripheral blood were obtained for in vitro studies from patients structure with newly diagnosed or recurrent AML with high blast count. Informed consent was obtained following institutional guidelines. Clinical data for AML patient samples used in the in vitro assays are presented in Table I.Patient karyotypes were obtained by conventional methods as part of the standard diagnostic workup, typically on samples derived from bone marrow. Samples were obtained from all patients prior to treatment. Mononuclear cells were isolated by centrifugation through Ficoll Hypaque density gradients. Samples from healthy bone marrow donors were selected for CD34þ cells using a Mini Macs magnetic antibody separation column as directed by the manufacturer. GENE EXPRESSION ANALYSIS Leukemia derived cell lines, blast cells from 75 AML patients, and CD34þ cells from six normal donors .
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