The inhibition of intrinsic expression of GFP in nasopharyngeal carcinoma by RNA interferencing
Yiqin Wang
Abstract
Yiqin Wang
Abstract
Objective:To construct a nasopharyngeal carcinoma cell strain expressing GFP stably and observe the inhibition effect and cytotoxicity of short hairpin RNA targeting the intrinsic GFP.Methods:HNE1 cells transfected with pEGFP-N1 were followed by the screening with G418 to obtain the stable nasopharyngeal carcinoma cell strain expressing GFP(HNE1-GFP);shGFP,a vector expressing short hairpin RNA targeting GFP,was transfected into HNE1-GFP with various levels.The fluorescence was observed by fluorescent microscope.The inhibition ratios and cytotoxicity of shRNA were analyzed by software and MTT,respectively;The protein and mRNA level of GFP were detected by Western Blot and RT-PCR,respectively.Results:The GFP gene was expressed stably within HNE1-GFP cell line;shGFP suppressed the intrinsic expression of GFP with the ratios of 49.7%,84.8% and 86.7%,respectively,without significant cytotoxicity.Conclusion:A nasopharyngeal carcinoma cell strain expressing GFP stably is established successfully;The inhibition effect of RNA interference is demonstrated in nasopharyngeal carcinoma cells and it is characterized by the significant concentration dependence and rare cytotoxicity.
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 construct a nasopharyngeal carcinoma cell strain expressing GFP stably and observe the inhibition effect and cytotoxicity of short hairpin RNA targeting the intrinsic GFP.Methods:HNE1 cells transfected with pEGFP-N1 were followed by the screening with G418 to obtain the stable nasopharyngeal carcinoma cell strain expressing GFP(HNE1-GFP);shGFP,a vector expressing short hairpin RNA targeting GFP,was transfected into HNE1-GFP with various levels.The fluorescence was observed by fluorescent microscope.The inhibition ratios and cytotoxicity of shRNA were analyzed by software and MTT,respectively;The protein and mRNA level of GFP were detected by Western Blot and RT-PCR,respectively.Results:The GFP gene was expressed stably within HNE1-GFP cell line;shGFP suppressed the intrinsic expression of GFP with the ratios of 49.7%,84.8% and 86.7%,respectively,without significant cytotoxicity.Conclusion:A nasopharyngeal carcinoma cell strain expressing GFP stably is established successfully;The inhibition effect of RNA interference is demonstrated in nasopharyngeal carcinoma cells and it is characterized by the significant concentration dependence and rare cytotoxicity.
Key concepts: Green fluorescent protein, Transfection, Cytotoxicity, Nasopharyngeal carcinoma, Molecular biology, Small hairpin RNA, Cell culture, RNA