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Journal Article

Citation

Lu S. Tumor 2007; (12): 515-517.

Copyright

(Copyright © 2007)

DOI

unavailable

PMID

unavailable

Abstract

OBJECTIVE: To evaluate the specific killing effects of the adenovirus-mediated transfer of cytosine deaminase gene and uracil phosphoribosyltransferase gene (CD::UPP) directed by the mdrl promoter combined with 5-fluorocytosine (5-FC) on Taxol-resistant ovarian cancer cells in vitro and in vivo.

METHODS: The adenovirus vector carrying the mdrl-CD :: UPP gene was amplified, purified, and transferred into Taxol-resistant A2780/Taxol ovarian cancer cells and A2780 cells. The expression of mdrl and CD :: UPP was detected by RT-PCR. After addition of 5-FC, the cell proliferation was assessed by MTT assay. The female BALB/c nude mice bearing tumor xenografts were injected adenovirus vector containing mdrl-CD :: UPP gene and then administered 5-FC. The growth of transplanted tumors was observed.

RESULTS: Mdrl and CD :: UPP gene were stably expressed in A2780/Taxol cells. The growth speed of A2780/Taxol cells was significantly slower than A2780 cells after transfection. Transfection of CD :: UPP gene combined with administration of 5-FC induced bystander effect of A2780/ Taxol cells on neighbor cells. The tumor growth in test group was significantly inhibited compared with control group (569.10 ± 187.93) mm3 vs (2 111.98 ± 230.82) mm3, P < 0.01.

CONCLUSION: The mdrl promoter in an adenovirus vector regulates the specific expression of CD :: UPP in A2780/Taxol cells. This system specifically kills Taxol-resistant ovarian cancer cells.


Language: zh

Keywords

Suicide; Gene therapy; Cytosine deaminase; Genes; mdr; Ovarian neoplasms; Transgenic; Uracil phosphoribosyltransferase

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