Ad-ING4 inhibits K562 cell growth.
- Author:
Xin YU
1
;
Hai-feng ZHANG
;
Jin-zhi WANG
;
Yu-feng XIE
;
Ji-cheng YANG
;
Jing-cheng MIAO
Author Information
- Publication Type:Journal Article
- MeSH: Adenoviridae; genetics; Animals; Apoptosis; genetics; Base Sequence; Carrier Proteins; genetics; Cell Cycle Proteins; genetics; Cell Proliferation; Genetic Vectors; Homeodomain Proteins; genetics; Humans; K562 Cells; Mice; Molecular Sequence Data; Mutagenesis, Site-Directed; Plasmids; genetics; Transfection; Transformation, Bacterial; Tumor Suppressor Proteins; genetics
- From: Chinese Journal of Hematology 2007;28(6):396-400
- CountryChina
- Language:Chinese
-
Abstract:
OBJECTIVETo observe the effect of recombinant adenovirus Ad-ING4 on K562 cells.
METHODSHuman ING4 recombinant transfer vector pAdTrack-CMV-ING4 was constructed by enzyme digest and ligation of human ING4 gene which was obtained through site specific point mutation of mouse ING4. The vector was co-transduced into BJ5183 E. coli with pAdEasy-1. The new recombinant adenovirus vector pAdEasy-1-pAdTrack-CMV-hING4 was transfected into QBI-293A cells. To obtain the ING4 recombined adenovirus (Ad-ING4). Ad-ING4 was used to infect K562 cells. The effect on K562 cells of ING4 was tested by LSCM FCM and immunohistochemistry.
RESULTSHuman ING4 recombinant adenovirus vector was constructed successfully, and high titre ING4 recombinant adenovirus (Ad-ING4) was obtained. ING4 can down-regulate the expression of bcl-2 and up-regulate expression of bax. The apoptosis of K562 cells induced by ING4 was proved by LSCM FCM and immunohistochemistry. The apoptosis rate was 19.7% (after 72h), which displayed significant difference compared with that of control groups (P < 0.01).
CONCLUSIONAd-ING4 can inhibit the growth of K562 cells and induce the cells apoptosis. The human ING4 recombinant adenoviral vector constructed might provide an approach to the target therapy of tumors.
