Abstract | BACKGROUND: MATERIALS AND METHODS: Cell growth inhibition was studied using the Propidium iodide (PI) assay. Cell cycle analysis and recovery were detected by flow cytometry. The expression levels of various proteins were detected by western blot. Inhibition of colony formation in H460 was checked in vitro. In vivo efficacy was studied in H460 xenograft model. RESULTS: The combination of P276-00 and VPA showed synergistic effect on p53+ and p53- NSCLC cell lines in antiproliferative assay at both constant and non-constant ratio with marked decrease in colony forming potential. Flow cytometric analysis confirmed a significant time dependent increase in apoptosis with 64% apoptotic population at 96 h compared to VPA (1%) and P276-00 (28%) alone (p < 0.0001). Incubation of the cells after treatment, in fresh medium without drugs, led to the recovery of cells treated with P276-00 alone but not the cells treated with the combination of both the drugs. The combination treatment up-regulated tumor suppressor proteins like p53, p21 and p27 along with down-regulation of proliferation and survival proteins viz. cyclin D1 and Bcl-2. This was also associated with the upregulation of the pro-apoptotic protein Bax and significant accumulation of hyperacetylated histones in the combination treatment. Interestingly, VPA in combination with P276-00 was much more effective as an antitumor agent than alone, in the H460 xenograft tumor model in SCID mice. CONCLUSIONS: This study indicates that the combination of HDAC inhibitor VPA with CDK inhibitor P276-00 is promising novel molecularly targeted therapeutic approach for NSCLC treatment.
|
Authors | Nitesh Shirsath, Maggie Rathos, Umesh Chaudhari, H Sivaramakrishnan, Kalpana Joshi |
Journal | Lung cancer (Amsterdam, Netherlands)
(Lung Cancer)
Vol. 82
Issue 2
Pg. 214-21
(Nov 2013)
ISSN: 1872-8332 [Electronic] Ireland |
PMID | 24051085
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
|
Copyright | Copyright © 2013. Published by Elsevier Ireland Ltd. |
Chemical References |
- Antineoplastic Agents
- Cell Cycle Proteins
- Flavones
- Histone Deacetylase Inhibitors
- Histones
- P276-00
- Protein Kinase Inhibitors
- Valproic Acid
- Cyclin-Dependent Kinases
|
Topics |
- Acetylation
- Animals
- Antineoplastic Agents
(pharmacology, toxicity)
- Apoptosis
(drug effects)
- Carcinoma, Non-Small-Cell Lung
(drug therapy, metabolism)
- Cell Cycle
(drug effects)
- Cell Cycle Proteins
(metabolism)
- Cell Line, Tumor
- Cyclin-Dependent Kinases
(antagonists & inhibitors, metabolism)
- Flavones
(pharmacology)
- Histone Deacetylase Inhibitors
(pharmacology, toxicity)
- Histones
(metabolism)
- Humans
- Lung Neoplasms
(drug therapy, metabolism)
- Mice
- Protein Kinase Inhibitors
(pharmacology)
- Tumor Stem Cell Assay
- Valproic Acid
(pharmacology, toxicity)
- Xenograft Model Antitumor Assays
|