Overexpression of Bcl-2 partly inhibits apoptosis of human cervical cancer SiHa cells induced by arsenic trioxide.

Abstract

OBJECTIVE:

To study the biological effect of arsenic trioxide (As2O3) on human cervical cancer SiHa cells and SiHa cells overexpressing bcl-2 gene.

METHODS:

SiHa cells with overexpression of Bcl-2 (SiHa-Bcl2 cells) were established by transfecting SiHa cells with Bcl-2 expression vector. The sensitivities of SiHa and SiHa-Bcl2 cells to As2O3 were determined using MTT (Thiazolyl blue) reduction and colony forming ability assay, morphological analysis, flow cytometric analysis, DNA agarose gel electrophoresis, in situ cell death detection (TUNEL), Northern blot, RT-PCR and Western blot.

RESULTS:

As2O3 inhibited the growth of SiHa cells and induced G2/M arrest and apoptosis of the cells. RT-PCR and Western blot analysis revealed that As2O3 induced SiHa cell apoptosis possibly via inhibiting the expression of HPV16 E7 and decreasing the expression of c-myc. However, we found that SiHa-Bcl2 cells partly resisted As2O3 induced apoptosis, which might be related to the prevention of the down-regulation of HPV16 E7 and c-myc gene expression. Nevertheless, As2O3 at a high concentration could still induce apoptosis of SiHa-Bcl2 cells mainly via decreasing Bcl-2 expression and slightly inhibiting viral gene expression.

CONCLUSION:

As2O3 is an inducer of the apoptosis of human cervical carcinoma cells and the cells overexpressing Bcl-2 can partly resist As2O3 induced apoptosis, but the exact mechanism is unclear.

• Authors: Y Deng, C Lin, J Zheng, M Fu, X Liang, J Chen, P Xiao, M Wu
• Journal: Chinese medical journal (Chin Med J (Engl)) Vol. 113 Issue 1 Pg. 84-8 (Jan 2000) ISSN: 0366-6999 [Print] China
• PMID: 11775218 (Publication Type: Journal Article)

Chemical References

• Antineoplastic Agents
• Arsenicals
• DNA, Neoplasm
• Oxides
• Proto-Oncogene Proteins
• Proto-Oncogene Proteins c-bcl-2
• Tumor Suppressor Protein p53
• bcl-2-Associated X Protein
• Arsenic Trioxide

Topics

• Antineoplastic Agents (pharmacology)
• Apoptosis (drug effects)
• Arsenic Trioxide
• Arsenicals (pharmacology)
• Cell Cycle (drug effects)
• Cell Survival (drug effects)
• DNA, Neoplasm (analysis)
• Female
• Humans
• Oxides (pharmacology)
• Proto-Oncogene Proteins (analysis)
• Proto-Oncogene Proteins c-bcl-2 (physiology)
• Tumor Suppressor Protein p53 (analysis)
• Uterine Cervical Neoplasms (pathology)
• bcl-2-Associated X Protein