AIM: To explore the feasibility of enhancing apoptosis-inducing effects of chemotherapeutic drugs on human gastric cancer cells by stable transfection of extrinsic Smac gene. METHODS: After Smac gene was transferred i...AIM: To explore the feasibility of enhancing apoptosis-inducing effects of chemotherapeutic drugs on human gastric cancer cells by stable transfection of extrinsic Smac gene. METHODS: After Smac gene was transferred into gastric cancer cell line MKN-45, subclone cells were obtained by persistent G_(418) selection. Cellular Smac gene expression was determined by RT-PCR and Western blotting. After treatment with mitomycin (MMC) as an apoptotic inducer, in vitro cell growth activities were investigated by trypan blue-staining method and MTT colorimetry. Cell apoptosis and its rates were determined by electronic microscopy, annexin V-FTTC and propidium iodide staining flow cytometry. Cellular caspase-3 protein expression and its activities were assayed by Western blotting and colorimetry. RESULTS: When compared with MKN-45 cells, the selected subclone cell line MKN-45/Smac had significantly higher Smac mRNA (3.12±0.21 vs 0.82±0.14, t=7.52, P＜0.01) and protein levels (4.02±0.24 vs0.98±0.11, t=8.32, P＜0.01). After treatment with 10 μg/mL MMC for 6-24 h, growth inhibition rate of MKN-45/Smac (15.8±1.2-54.8±2.9%) was significantly higher than that of MKN-45 (5.8±0.4-24.0±1.5%, t=6.42, P＜0.01). Partial MKN-45/Smac cancer cells presented characteristic morphological changes of apoptosis under the electronic microscope with an apoptosis rate of 36.4±2.1%, which was significantly higher than that of MKN-45 (15.2±0.8%, t=9.25, P＜0.01). Compared with MKN-45, caspase-3 expression levels in MKN-45/Smac were improved significantly (3.39±0.42 vs0.96±0.14, t=8.63, P＜0.01), while its activities were 3.25 times as many as those of MKN-45 (0.364±0.010 vs0.112±0.007, t=6.34, P＜0.01). CONCLUSION: Stable transfection of extrinsic Smac gene and its over-expression in gastric cancer cell line can significantly enhance cellular caspase-3 expression and activities, ameliorate apoptosis-inducing effects of mitomycin C on cancer cells, which is a novel strategy to improve chemotherapeutic effects on gastric cancer.展开更多
To construct an eukaryotic expression vector containing Smac gene and study the expression efficiency and specificity of prostate specific antigen（PSA） enhancer/promoter in a possible targeted gene therapy scheme fo...To construct an eukaryotic expression vector containing Smac gene and study the expression efficiency and specificity of prostate specific antigen（PSA） enhancer/promoter in a possible targeted gene therapy scheme for prostate cancer. Methods： PSA enhancer （PSAE） and promoter （PSAP） sequences were amplified using PCR method. CMV and T7 promoters were deleted from pcDNA3.1-Smac and replaced by the two specific fragments to generate pPSAE-PSAP-Smac. After transfection into different cell lines, the status of cells was observed. And then, we determined the relative concentration of Smac mRNA in RT-PCR. Results： The recombinant plasmid of pPSAE-PSAP-Smac was successfully constructed. And only the prostate cancer cell line PC-3 was suppressed after transfection with pPSAE-PSAP-Smac. However, other nonprostate lines were not. Moreover, the concentration of Smac mRNA regulated by PSA promoter and enhancer was higher in comparison to the CMV promoter-driven control vectors. Conclusion： An expression vector containing the Smac gene （based on elements of the PSA gene regulatory sequences） has been developed and shown to function in prostate cancer cell lines which provides a solid platform for launching clinical studies.展开更多
The second mitochondria-derived activator of caspases (Smac) is a novelproapoptotic gene, which plays an important role in the apoptosis-inducing effects of irradiation ontumor cells. The purpose of this study was to ...The second mitochondria-derived activator of caspases (Smac) is a novelproapoptotic gene, which plays an important role in the apoptosis-inducing effects of irradiation ontumor cells. The purpose of this study was to investigate the effects of extrinsic Smac genetransfer and its over-expression in radiotherapeutic sensitivities of cervical cancer cells. Afterthe Smac gene was transferred into the cervical cancer cell line HeLa, subcloned cells were obtainedby persistent G418 selection. Cellular Smac gene expression was detected by RT-PCR and Westernblot, while in vitro cell viabilities were detected by trypan blue staining assay. After treatmentwith X-ray irradiation, cellular radiotherapeutic sensitivities were investigated by tetrazoliumbromide colorimetry. Cellular apoptosis and its rate were determined by electronic microscopy,annexin V-FITC and propidium iodide staining flow cytometry. The expression and activities ofcellular caspase-3 were assayed by Western blot and colorimetry. Smac mRNA and protein levels inHeLa/Smac cells and the selected subclone cell line of cervical cancer were significantly higherthan those of HeLa (P <0. 01). There was no significant difference in cellular viabilities betweenthem (P > 0. 05 ) . However, after irradiation with 8 Gy X-ray, growth activities of HeLa/ Smac werereduced by 22.42% (P < 0. 01). When compared with those of HeLa, partial HeLa/Smac cells presentedcharacteristic morphological changes of apoptosis under electronic microscope, with higher apoptosisrates (16. 4% vs. 6. 2% , P < 0. 01 ) ; the caspase-3 expression levels in HeLa/Smac cells wereimproved significantly (P <0. 01) , while its activities were increased by 3. 42 times (P <0. 01).Stable transfer of the extrinsic Smac gene and its over-expression in cervical cancer cell linecould significantly enhance the expression and activities of cellular caspase-3 and ameliorateapoptosis-inducing effects of irradiation on cancer cells, which was a novel strategy to improveradiotherapeutic effects on cervical cancer.展开更多
文摘AIM: To explore the feasibility of enhancing apoptosis-inducing effects of chemotherapeutic drugs on human gastric cancer cells by stable transfection of extrinsic Smac gene. METHODS: After Smac gene was transferred into gastric cancer cell line MKN-45, subclone cells were obtained by persistent G_(418) selection. Cellular Smac gene expression was determined by RT-PCR and Western blotting. After treatment with mitomycin (MMC) as an apoptotic inducer, in vitro cell growth activities were investigated by trypan blue-staining method and MTT colorimetry. Cell apoptosis and its rates were determined by electronic microscopy, annexin V-FTTC and propidium iodide staining flow cytometry. Cellular caspase-3 protein expression and its activities were assayed by Western blotting and colorimetry. RESULTS: When compared with MKN-45 cells, the selected subclone cell line MKN-45/Smac had significantly higher Smac mRNA (3.12±0.21 vs 0.82±0.14, t=7.52, P＜0.01) and protein levels (4.02±0.24 vs0.98±0.11, t=8.32, P＜0.01). After treatment with 10 μg/mL MMC for 6-24 h, growth inhibition rate of MKN-45/Smac (15.8±1.2-54.8±2.9%) was significantly higher than that of MKN-45 (5.8±0.4-24.0±1.5%, t=6.42, P＜0.01). Partial MKN-45/Smac cancer cells presented characteristic morphological changes of apoptosis under the electronic microscope with an apoptosis rate of 36.4±2.1%, which was significantly higher than that of MKN-45 (15.2±0.8%, t=9.25, P＜0.01). Compared with MKN-45, caspase-3 expression levels in MKN-45/Smac were improved significantly (3.39±0.42 vs0.96±0.14, t=8.63, P＜0.01), while its activities were 3.25 times as many as those of MKN-45 (0.364±0.010 vs0.112±0.007, t=6.34, P＜0.01). CONCLUSION: Stable transfection of extrinsic Smac gene and its over-expression in gastric cancer cell line can significantly enhance cellular caspase-3 expression and activities, ameliorate apoptosis-inducing effects of mitomycin C on cancer cells, which is a novel strategy to improve chemotherapeutic effects on gastric cancer.
基金This work was supported by National Natural Science Foundation of China(30271301)
文摘To construct an eukaryotic expression vector containing Smac gene and study the expression efficiency and specificity of prostate specific antigen（PSA） enhancer/promoter in a possible targeted gene therapy scheme for prostate cancer. Methods： PSA enhancer （PSAE） and promoter （PSAP） sequences were amplified using PCR method. CMV and T7 promoters were deleted from pcDNA3.1-Smac and replaced by the two specific fragments to generate pPSAE-PSAP-Smac. After transfection into different cell lines, the status of cells was observed. And then, we determined the relative concentration of Smac mRNA in RT-PCR. Results： The recombinant plasmid of pPSAE-PSAP-Smac was successfully constructed. And only the prostate cancer cell line PC-3 was suppressed after transfection with pPSAE-PSAP-Smac. However, other nonprostate lines were not. Moreover, the concentration of Smac mRNA regulated by PSA promoter and enhancer was higher in comparison to the CMV promoter-driven control vectors. Conclusion： An expression vector containing the Smac gene （based on elements of the PSA gene regulatory sequences） has been developed and shown to function in prostate cancer cell lines which provides a solid platform for launching clinical studies.
文摘The second mitochondria-derived activator of caspases (Smac) is a novelproapoptotic gene, which plays an important role in the apoptosis-inducing effects of irradiation ontumor cells. The purpose of this study was to investigate the effects of extrinsic Smac genetransfer and its over-expression in radiotherapeutic sensitivities of cervical cancer cells. Afterthe Smac gene was transferred into the cervical cancer cell line HeLa, subcloned cells were obtainedby persistent G418 selection. Cellular Smac gene expression was detected by RT-PCR and Westernblot, while in vitro cell viabilities were detected by trypan blue staining assay. After treatmentwith X-ray irradiation, cellular radiotherapeutic sensitivities were investigated by tetrazoliumbromide colorimetry. Cellular apoptosis and its rate were determined by electronic microscopy,annexin V-FITC and propidium iodide staining flow cytometry. The expression and activities ofcellular caspase-3 were assayed by Western blot and colorimetry. Smac mRNA and protein levels inHeLa/Smac cells and the selected subclone cell line of cervical cancer were significantly higherthan those of HeLa (P <0. 01). There was no significant difference in cellular viabilities betweenthem (P > 0. 05 ) . However, after irradiation with 8 Gy X-ray, growth activities of HeLa/ Smac werereduced by 22.42% (P < 0. 01). When compared with those of HeLa, partial HeLa/Smac cells presentedcharacteristic morphological changes of apoptosis under electronic microscope, with higher apoptosisrates (16. 4% vs. 6. 2% , P < 0. 01 ) ; the caspase-3 expression levels in HeLa/Smac cells wereimproved significantly (P <0. 01) , while its activities were increased by 3. 42 times (P <0. 01).Stable transfer of the extrinsic Smac gene and its over-expression in cervical cancer cell linecould significantly enhance the expression and activities of cellular caspase-3 and ameliorateapoptosis-inducing effects of irradiation on cancer cells, which was a novel strategy to improveradiotherapeutic effects on cervical cancer.
