2013•Unpublished venueRequires access

The research of human prostate cancer PC3 、LNCaP apoptosis induced by siRNA mediated survivin gene silencing

Jianguang Liu, Yang Jinyi

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Abstract

Objectives To study the influence of siRNA to the expression of survivin and the prostate cancer PC3 、LNCaP cell apoptosis.Methods Design 2 siRNA sequences aim at survivin genes,using siRNA design software; PC3,LNCaP cell culture,take siRNA into PC3 、LNCaP cells,through the liposome; MTT method to detect the proliferation of cells inhibition rate (IR) ; Flow cytometry to detect cell apoptosis; Half quantitative RT-PCR detection survivin mRNA expression level ; Western Blotting detection survivin protein expression strength.Results siRNA 2 groups of PC3 cells of proliferation inhibition rate (IR) after transfection:43.84%,54.31% ; Apoptosis index (AI):22.3%,30.34%; Significantly higher than normal control group PC3 cells of proliferation inhibition rate (IR):2.40% and apoptosis index (AI):3.81% ; LNCaP cell proliferation of inhibition rate (IR):41.78%,53.31% ; Apoptosis index (AI):18.33%,28.44% ;Significantly higher than normal control group LNCaP cell proliferation of inhibition rate (IR):1.97% and apoptosis index (AI):3.43%.Conclusions siRNA can inhibits the expression of survivin in PC3 、LNCaP cells,induce cell apoptosis,provide the trial basis for prostate cancer,especially metastatic castration-resistant prostate cancer. Key words: Prostatic Neoplasms;  Apoptosis

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Objectives To study the influence of siRNA to the expression of survivin and the prostate cancer PC3 、LNCaP cell apoptosis.Methods Design 2 siRNA sequences aim at survivin genes,using siRNA design software; PC3,LNCaP cell culture,take siRNA into PC3 、LNCaP cells,through the liposome; MTT method to detect the proliferation of cells inhibition rate (IR) ; Flow cytometry to detect cell apoptosis; Half quantitative RT-PCR detection survivin mRNA expression level ; Western Blotting detection survivin protein expression strength.Results siRNA 2 groups of PC3 cells of proliferation inhibition rate (IR) after transfection:43.84%,54.31% ; Apoptosis index (AI):22.3%,30.34%; Significantly higher than normal control group PC3 cells of proliferation inhibition rate (IR):2.40% and apoptosis index (AI):3.81% ; LNCaP cell proliferation of inhibition rate (IR):41.78%,53.31% ; Apoptosis index (AI):18.33%,28.44% ;Significantly higher than normal control group LNCaP cell proliferation of inhibition rate (IR):1.97% and apoptosis index (AI):3.43%.Conclusions siRNA can inhibits the expression of survivin in PC3 、LNCaP cells,induce cell apoptosis,provide the trial basis for prostate cancer,especially metastatic castration-resistant prostate cancer. Key words: Prostatic Neoplasms;  Apoptosis

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Available abstract

Objectives To study the influence of siRNA to the expression of survivin and the prostate cancer PC3 、LNCaP cell apoptosis.Methods Design 2 siRNA sequences aim at survivin genes,using siRNA design software; PC3,LNCaP cell culture,take siRNA into PC3 、LNCaP cells,through the liposome; MTT method to detect the proliferation of cells inhibition rate (IR) ; Flow cytometry to detect cell apoptosis; Half quantitative RT-PCR detection survivin mRNA expression level ; Western Blotting detection survivin protein expression strength.Results siRNA 2 groups of PC3 cells of proliferation inhibition rate (IR) after transfection:43.84%,54.31% ; Apoptosis index (AI):22.3%,30.34%; Significantly higher than normal control group PC3 cells of proliferation inhibition rate (IR):2.40% and apoptosis index (AI):3.81% ; LNCaP cell proliferation of inhibition rate (IR):41.78%,53.31% ; Apoptosis index (AI):18.33%,28.44% ;Significantly higher than normal control group LNCaP cell proliferation of inhibition rate (IR):1.97% and apoptosis index (AI):3.43%.Conclusions siRNA can inhibits the expression of survivin in PC3 、LNCaP cells,induce cell apoptosis,provide the trial basis for prostate cancer,especially metastatic castration-resistant prostate cancer. Key words: Prostatic Neoplasms;  Apoptosis

Key concepts: Survivin, LNCaP, Apoptosis, Gene silencing, Cancer research, Cell growth, Prostate cancer, MTT assay

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