Abstract | OBJECTIVE: To study the effects of recombinant adenovirus with RA538 or antisense c-myc insert on cervical cancer cell lines with high expression of bcl-2 gene. METHODS:
Cervical cancer cell lines HeLa and SiHa were transduced with full length bcl-2 cDNA by lipofectin and cell clones with stable expression of bcl-2 were selected. They were then transfected with recombinant adenovirus containing RA538 (Ad-RA538), antisense c-myc (Ad-ASc-myc) or LacZ (Ad-LacZ) gene. Morphologic and molecular changes of the transfected cancer cells were examined by light microscopy, MTT, RT-PCR and Northern blot. RESULTS: The bcl-2 cDNA was successfully transferred into HeLa and SiHa cells. Two cell lines, called HeLa-bcl2 and SiHa-bcl2 with high expression of bcl-2 gene were generated. Ad-RA538 and Ad-ASc-myc transfection both could inhibit cell growth and induce apoptosis of HeLa and SiHa cells, and inhibit their expression of c-myc and bcl-2 genes. However, although Ad-RA538 and Ad-ASc-myc had some inhibitory effect on bcl-2 and c-myc gene expression by HeLa-bcl2 and SiHa-bcl2 cells, they could only slightly inhibit cell growth and weakly induce apoptosis. CONCLUSION: Ad-RA538 and Ad-ASc-myc can to certain extent inhibit cell growth and induce apoptosis of two cervical cancer cell lines. They have little such effect when these cell lines have over-expressed bcl-2 by transduction of exogenous bcl-2 gene.
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Authors | J Chen, C Lin, Y Deng |
Journal | Zhonghua zhong liu za zhi [Chinese journal of oncology]
(Zhonghua Zhong Liu Za Zhi)
Vol. 22
Issue 4
Pg. 279-82
(Jul 2000)
ISSN: 0253-3766 [Print] China |
PMID | 11778549
(Publication Type: English Abstract, Journal Article)
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Chemical References |
- Antineoplastic Agents
- DNA, Antisense
- Proto-Oncogene Proteins c-bcl-2
- Proto-Oncogene Proteins c-myc
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Topics |
- Antineoplastic Agents
(pharmacology)
- Antineoplastic Combined Chemotherapy Protocols
(pharmacology)
- Apoptosis
- Cell Division
(drug effects)
- DNA, Antisense
(pharmacology)
- Female
- HeLa Cells
- Humans
- Proto-Oncogene Proteins c-bcl-2
(drug effects, metabolism)
- Proto-Oncogene Proteins c-myc
(antagonists & inhibitors, genetics, metabolism)
- Tumor Cells, Cultured
- Uterine Cervical Neoplasms
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