Selective cytotoxic effect of lentivirus-mediated double suicide gene transfer on human gastric adneocarcinoma cells.
- Author:
Heng KONG
1
;
Zong-hai HUANG
;
Hai-jin CHEN
;
Qiang LI
;
Lin-yu TAO
;
Ke QI
Author Information
- Publication Type:Journal Article
- MeSH: Adenocarcinoma; genetics; pathology; Cell Line, Tumor; Cytosine Deaminase; biosynthesis; genetics; Cytotoxins; pharmacology; Genes, Transgenic, Suicide; genetics; Genetic Therapy; Genetic Vectors; genetics; Humans; Lentivirus; genetics; metabolism; Recombinant Fusion Proteins; biosynthesis; genetics; pharmacology; Stomach Neoplasms; genetics; pathology; Thymidine Kinase; biosynthesis; genetics; Vascular Endothelial Growth Factor Receptor-2; genetics; metabolism
- From: Journal of Southern Medical University 2010;30(1):47-50
- CountryChina
- Language:Chinese
-
Abstract:
OBJECTIVETo study the selective cytotoxic effect of lentivirus-mediated double suicide gene (CD/TK) against human gastric carcinoma cells SGC-7901 in vitro.
METHODSSGC-7901 cells were infected with FGW-KDRP-CD/TK vector and the infection efficiency was observed under a fluorescence microscope. The morphological changes of the infected cells were observed by Giemsa staining. Flow cytometry (FCM) was employed for cell cycle analysis, and the expression of CD/TK was detected by RT-PCR. The infected cells were then treated with the prodrugs ganciclovir (GCV) and/or 5-fluorocytosine (5-FC) at different concentrations, and the cytotoxic effects were evaluated using MTT method.
RESULTSThe infection efficiency of the lentiviral vector in SGC-7901 cells increased with the titer of the virus, which produced no significant effect on the cancer cell morphology in vitro or on the percentages of G0-G1, G2-M and S phase cells (P>0.05). RT-PCR demonstrated the expression of CD/TK gene in SGC-7901 cells infected by FGW-KDRP-CD/TK. The infected cells were highly sensitive to the prodrugs with a dose-dependent cytotoxic effect within a specific concentration range of the drugs, whereas the non-infected cells were not sensitive to the prodrugs. Combined use of the two prodrugs produced an obviously stronger inhibitory effect than either of the them (P<0.05). When combined, GCV and 5-FC at the concentration of 0.1+40, 1+80, 10+160, and 100+320 mg/L demonstrated a synergetic effect with a CDI<1.
CONCLUSIONLentivirus-mediated CD/TK fusion gene system can selectively kill gastric cancer cells, and the two prodrugs show a synergistic cytotoxic effect.