实用临床医药杂志
實用臨床醫藥雜誌
실용림상의약잡지
JOURNAL OF JIANGSU CLINICAL MEDICINE
2014年
16期
14-17
,共4页
樊玉祥%曾凡业%何文婷%张洪亮
樊玉祥%曾凡業%何文婷%張洪亮
번옥상%증범업%하문정%장홍량
β-咔啉类生物碱%人胃癌 SGC-7901%细胞增殖%细胞凋亡
β-咔啉類生物堿%人胃癌 SGC-7901%細胞增殖%細胞凋亡
β-잡람류생물감%인위암 SGC-7901%세포증식%세포조망
β-Carboline alkaloids%SGC-7901%proliferation%apoptosis
目的:探讨β-咔啉类生物碱对人胃癌细胞 SGC-7901增殖的影响。方法通过体外培养人胃癌细胞株 SGC-7901,将含有不同浓度(5、10、20、40μg/mL)β-咔啉类生物碱的培养液与 SGC-7901细胞共同培养24 h 和48 h。采用 MTT 比色法计算细胞抑制率;在荧光显微镜下用 Hoechst 33258细胞核染色法观察细胞形态学改变;流式细胞仪检测凋亡率及基因组DNA 琼脂凝胶电泳检测凋亡梯状条带。结果β-咔啉类生物碱对 SGC-7901细胞的损伤呈浓度依赖性;β-咔啉类生物碱分别作用24 h 和48 h 后半数抑制浓度(IC50)分别为17.79μg/mL 和12.17μg/mL;荧光染色可观察到有细胞核固缩及核断裂的凋亡现象;流式细胞术显示:阴性对照组(0μg/mL)及β-咔啉类生物碱5、10、20、40μg/mL 浓度组24、48 h 凋亡率为别1.66%、11.27%、20.32%、30.66%、41.42%和3.84%、15.29%、23.34%、34.87%、49.54%,细胞凋亡率伴随给药浓度增加而增加;基因组 DNA 琼脂糖凝胶电泳检测到明显的凋亡梯状条带。结论β-咔啉类生物碱能诱导人胃癌 SGC-7901细胞发生凋亡,抑制细胞增殖。
目的:探討β-咔啉類生物堿對人胃癌細胞 SGC-7901增殖的影響。方法通過體外培養人胃癌細胞株 SGC-7901,將含有不同濃度(5、10、20、40μg/mL)β-咔啉類生物堿的培養液與 SGC-7901細胞共同培養24 h 和48 h。採用 MTT 比色法計算細胞抑製率;在熒光顯微鏡下用 Hoechst 33258細胞覈染色法觀察細胞形態學改變;流式細胞儀檢測凋亡率及基因組DNA 瓊脂凝膠電泳檢測凋亡梯狀條帶。結果β-咔啉類生物堿對 SGC-7901細胞的損傷呈濃度依賴性;β-咔啉類生物堿分彆作用24 h 和48 h 後半數抑製濃度(IC50)分彆為17.79μg/mL 和12.17μg/mL;熒光染色可觀察到有細胞覈固縮及覈斷裂的凋亡現象;流式細胞術顯示:陰性對照組(0μg/mL)及β-咔啉類生物堿5、10、20、40μg/mL 濃度組24、48 h 凋亡率為彆1.66%、11.27%、20.32%、30.66%、41.42%和3.84%、15.29%、23.34%、34.87%、49.54%,細胞凋亡率伴隨給藥濃度增加而增加;基因組 DNA 瓊脂糖凝膠電泳檢測到明顯的凋亡梯狀條帶。結論β-咔啉類生物堿能誘導人胃癌 SGC-7901細胞髮生凋亡,抑製細胞增殖。
목적:탐토β-잡람류생물감대인위암세포 SGC-7901증식적영향。방법통과체외배양인위암세포주 SGC-7901,장함유불동농도(5、10、20、40μg/mL)β-잡람류생물감적배양액여 SGC-7901세포공동배양24 h 화48 h。채용 MTT 비색법계산세포억제솔;재형광현미경하용 Hoechst 33258세포핵염색법관찰세포형태학개변;류식세포의검측조망솔급기인조DNA 경지응효전영검측조망제상조대。결과β-잡람류생물감대 SGC-7901세포적손상정농도의뢰성;β-잡람류생물감분별작용24 h 화48 h 후반수억제농도(IC50)분별위17.79μg/mL 화12.17μg/mL;형광염색가관찰도유세포핵고축급핵단렬적조망현상;류식세포술현시:음성대조조(0μg/mL)급β-잡람류생물감5、10、20、40μg/mL 농도조24、48 h 조망솔위별1.66%、11.27%、20.32%、30.66%、41.42%화3.84%、15.29%、23.34%、34.87%、49.54%,세포조망솔반수급약농도증가이증가;기인조 DNA 경지당응효전영검측도명현적조망제상조대。결론β-잡람류생물감능유도인위암 SGC-7901세포발생조망,억제세포증식。
Objective To investigate the effects of β-Carboline of alkaloids on proliferation of SGC-7901 of human gastric cancer cells.Methods SGC-7901 cells were cultured in vitro initially. After SGC-7901 cells were incubated with β-Carboline alkaloids at different concentrations of 5,10, 20,40 μg/mL for 24,48 hours,the inhibited proliferation rate of SGC-7901 cells were examined by Methtl Thiazolyl Tetrazolium(MTT)assay.Morphological changes of SGC-7901 cells were observed by Hoechst 33258 under fluorescence microscope.Flow cytometry was used to detect cell apoptosis after SGC-7901 cells were incubated with β-Carboline alkaloids for 24 hours.Cell gemonic DNA was detec-ted by agarose electrophoresis.Results β-Carboline of alkaloids induced damage of SGC-7901 cell in a concentration dependent manner .The IC 5 0 of β-Carboline alkaloids at 2 4 ,4 8 hours were 17.79 μg/mL and 12.17 μg/mL respectively.Apoptotic cells were observed and flow cytonetry analy-sis in dicated that the apoptosis rate of cells treated with different concentrations of β-Carboline alka-loids(0,5,10,20,40 μg/mL)for 24 and 48 hours were 1.66%,11.27%,20.32%,30.66%, 41.42%;3.84%,15.29%,23.34%,34.87%,49.54%,respectively.Increasing in apoptosis rate of SGC-7901 cells was associated with drug concentration.Typical DNA Ladder was detected in DNA agarose electrophoresis.Conclusion β-Carboline alkaloids can inhibit the proliferation and in-duce the apoptosis of SGC-7901 cells.