The effect of DHA compound on Bcl-2 and Bax mRNA transcription in U251 glioma
Sun Ken-ren
Abstract
Sun Ken-ren
Abstract
Objective To study the anticancer mechanism of DHA compound.Methods The in vitro effect was assessed by cell-culture.RT-PCR was used to investigate the effects of DHA compound on Bcl-2 and Bax mRNA transcription in U251 glioma cell.Results The IC50 of DHA compound on U251 glioma cell was 0.3746 μg/ml(0.3324~0.4168 μg/ml);Compared with control,the content of Bcl-2 mRNA was decreasd significantly and content of Bax mRNA was increased significantly in U251 glioma cell after treated with DHA compound.Conclusion The proliferation of the U251 glioma cell was inhibited by DHA compound.The transcrisption of Bcl-2 was decreased and the transcrisption of Bax mRNA was increased in U251 glioma cell after treated with DHA compound and thus the apoptosis of the cancer cell was promoted.
A significance statement is not available in the OpenAlex record.
A contribution statement is not available in the OpenAlex record.
Method details are not available in the OpenAlex metadata.
Findings are not separately available in the OpenAlex metadata.
Limitations are not available in the OpenAlex metadata.
Application details are not available in the OpenAlex metadata.
Objective To study the anticancer mechanism of DHA compound.Methods The in vitro effect was assessed by cell-culture.RT-PCR was used to investigate the effects of DHA compound on Bcl-2 and Bax mRNA transcription in U251 glioma cell.Results The IC50 of DHA compound on U251 glioma cell was 0.3746 μg/ml(0.3324~0.4168 μg/ml);Compared with control,the content of Bcl-2 mRNA was decreasd significantly and content of Bax mRNA was increased significantly in U251 glioma cell after treated with DHA compound.Conclusion The proliferation of the U251 glioma cell was inhibited by DHA compound.The transcrisption of Bcl-2 was decreased and the transcrisption of Bax mRNA was increased in U251 glioma cell after treated with DHA compound and thus the apoptosis of the cancer cell was promoted.
Key concepts: Glioma, Apoptosis, Messenger RNA, Cell, Chemistry, Transcription (linguistics), Cell culture, In vitro