Role of homeobox gene A5 in multidrug resistance of human small cell lung cancer cells.
- Author:
Faman XIAO
1
;
Zhenzhu CHEN
;
Xiangping ZENG
;
Yifeng BAI
;
Linlang GUO
;
Yufa LI
Author Information
- Publication Type:Journal Article
- MeSH: Antineoplastic Agents; pharmacology; Antineoplastic Agents, Phytogenic; pharmacology; Cell Line, Tumor; Cell Survival; drug effects; Cisplatin; pharmacology; Drug Resistance, Multiple; Drug Resistance, Neoplasm; Etoposide; pharmacology; Homeodomain Proteins; genetics; metabolism; Humans; Immunoblotting; Lung Neoplasms; metabolism; pathology; Plasmids; RNA, Messenger; metabolism; RNA, Small Interfering; genetics; Real-Time Polymerase Chain Reaction; Small Cell Lung Carcinoma; metabolism; pathology; Transfection
- From: Journal of Southern Medical University 2013;33(11):1665-1668
- CountryChina
- Language:Chinese
-
Abstract:
OBJECTIVETo investigate the role of homeobox gene A5 (HOXA5) in multidrug resistance of human small cell lung cancer (SCLC) cells and the possibility of using HOXA5 as the therapeutic targets for SCLC treatment.
METHODSWe examined HOXA5 mRNA and protein expressions in chemosensitive human SCLC cells (H69) and the multidrug-resistant SCLC cells (H69AR) using quantitative real-time PCR and immunoblotting. HOXA5 expression was then enhanced or suppressed by transfection of the cells with HOXA5 expression plasmids or small interference RNA (siRNA), and the chemosensitivity of transfected cells to cisplatin (DDP) and etoposide (VP-16) was evaluated using cell counting kit-8 (CCK8) assay.
RESULTSH69 cells showed a 8.99-fold higher expression of HOXA5 than H69AR cells. HOXA5 knockdown caused obvious reductions in the chemosensitivity of H69 cells to DDP and VP-16 with increased cells in G0/G1 phase; conversely, HOXA5 enhancement resulted in an increased sensitivity of H69AR cells to DDP and VP-16.
CONCLUSIONHOXA5 may play an important role in multidrug resistance of SCLC and can be a potential therapeutic target in clinical treatment of SCLC.
