Quantitative analysis of gene expression for vascular endothelial growth factor and its application.
- Author:
Xia BAI
1
;
Jian-Xin FU
;
Kai-Yang DING
;
Jian-Nong CEN
;
Wei WANG
;
Chang-Geng RUAN
Author Information
1. Jiangsu Institute of Hematology, The First Affiliated Hospital of Suzhou University, Suzhou 215006, China.
- Publication Type:Journal Article
- MeSH:
Antineoplastic Agents;
pharmacology;
CD11b Antigen;
genetics;
Cell Differentiation;
drug effects;
genetics;
Cell Line, Tumor;
Gene Expression Regulation, Neoplastic;
drug effects;
Humans;
Leukemia, Promyelocytic, Acute;
genetics;
pathology;
Molecular Sequence Data;
Reverse Transcriptase Polymerase Chain Reaction;
methods;
Tretinoin;
pharmacology;
Vascular Endothelial Growth Factor A;
genetics
- From:
Journal of Experimental Hematology
2005;13(4):548-552
- CountryChina
- Language:Chinese
-
Abstract:
Vascular endothelial growth factor (VEGF), a central mediator of angiogenesis, not only plays an important role in the pathogenesis of leukemia, but also is an independent prognostic factor in patients with hematologic malignancies, like those in solid tumors. However, the importance of VEGF during differentiation or apoptosis of leukemia cells remains to be elucidated. In order to assess the alternation of VEGF gene expression in the process of all-trans retinoic acid (ATRA)-induced differentiation of NB4 acute promyelocytic leukemia cell line, and a competitor DNA fragment, VEGF gene competative template (T-VEGFDelta) was constructed by using gene recombinant technologies, and a competitive quantitative reverse transcriptase-polymerase chain reaction (cQRT-PCR) method was developed. A standard curve was obtained by co-amplification of serial dilutions of the target nulecules with constant amount of competitive template and this curve was used to detect molecular number of target gene in measuring sample. The surface expression of CD11b antigen and nitroblue tetrazolium (NBT) reduction rate of NB4 cells were also assayed at different time points. The results showed that cQRT-PCR was a sensitive, reliable tool for analysis of VEGF gene expression with a detectable range from 1 x 10(4) to 2 x 10(5) molecules. The number of VEGF gene transcripts detected by means of cQRT-PCR assay was 42.3 x 10(5), 12.6 x 10(5), 3.6 x 10(5), and less than 1.0 x 10(5)/microg total RNA at 0, 12, 24 and 48 hours after ATRA treatment, respectively. This rapid down-regulation of VEGF gene expression, during ATRA-induced NB4 cell differentiation, was accompanied by the up-regulation of CD11b expression and an increased NBT reduction rate. In conclusion, cQRT-PCR method was successtully constructed, confirming that ATRA efficiently repressed VEGF, at the same time, the ATRA might exert an antileukemic effect, other than induction of differentiation via inhibition of angiogenesis.
