山西医药杂志
山西醫藥雜誌
산서의약잡지
SHANXI MEDICAL JOURNAL
2013年
23期
1342-1344
,共3页
张博威%张叶飞%黄江波%董尚波
張博威%張葉飛%黃江波%董尚波
장박위%장협비%황강파%동상파
膀胱肿瘤%微小RNAs%转染%细胞凋亡
膀胱腫瘤%微小RNAs%轉染%細胞凋亡
방광종류%미소RNAs%전염%세포조망
Bladder neoplasms%Micro RNAs%Transfection%Apoptosis
目的探讨和研究hsa-miR-340表达上调对人膀胱癌T24细胞增殖、凋亡能力的影响。方法化学合成hsa-miR-340模拟物,瞬时转染膀胱癌T24细胞,以实时荧光定量聚合酶链反应(RT-PCR)检测hsa-miR-340在膀胱癌T24细胞中相对表达量,确定能够转染成功并有较高的转染率后,分别通过四甲基偶氮唑蓝(MTT)法和流式细胞计数仪,分析转染hsa-miR-340模拟物前后对膀胱癌T24细胞的增殖及凋亡能力的影响。结果①hsa-miR-340模拟物可在膀胱癌T24细胞中表达,并以RT-PCR验证相对含量较高,差异有统计学意义(P<0.05)。②增殖实验中分别在48h和72h时把实验组与阴性对照组和空白对照组相对比,膀胱癌T24细胞生长增殖明显受抑制且差异有统计学意义(P<0.05),说明hsa-miR-340过表达后,能使T24细胞增殖能力受到有效抑制。③hsa-miR-340模拟物转染T24细胞48h后,以流式细胞仪检测T24细胞凋亡率,分别为实验组(11.37±0.41)%、阴性对照组(6.72±0.32)%、空白对照组(6.62±0.23)%,比较后差异有统计学意义(P<0.05),说明hsa-miR-340过表达使T24细胞的凋亡显著增加。结论hsa-miR-340可能参与膀胱癌的进展。
目的探討和研究hsa-miR-340錶達上調對人膀胱癌T24細胞增殖、凋亡能力的影響。方法化學閤成hsa-miR-340模擬物,瞬時轉染膀胱癌T24細胞,以實時熒光定量聚閤酶鏈反應(RT-PCR)檢測hsa-miR-340在膀胱癌T24細胞中相對錶達量,確定能夠轉染成功併有較高的轉染率後,分彆通過四甲基偶氮唑藍(MTT)法和流式細胞計數儀,分析轉染hsa-miR-340模擬物前後對膀胱癌T24細胞的增殖及凋亡能力的影響。結果①hsa-miR-340模擬物可在膀胱癌T24細胞中錶達,併以RT-PCR驗證相對含量較高,差異有統計學意義(P<0.05)。②增殖實驗中分彆在48h和72h時把實驗組與陰性對照組和空白對照組相對比,膀胱癌T24細胞生長增殖明顯受抑製且差異有統計學意義(P<0.05),說明hsa-miR-340過錶達後,能使T24細胞增殖能力受到有效抑製。③hsa-miR-340模擬物轉染T24細胞48h後,以流式細胞儀檢測T24細胞凋亡率,分彆為實驗組(11.37±0.41)%、陰性對照組(6.72±0.32)%、空白對照組(6.62±0.23)%,比較後差異有統計學意義(P<0.05),說明hsa-miR-340過錶達使T24細胞的凋亡顯著增加。結論hsa-miR-340可能參與膀胱癌的進展。
목적탐토화연구hsa-miR-340표체상조대인방광암T24세포증식、조망능력적영향。방법화학합성hsa-miR-340모의물,순시전염방광암T24세포,이실시형광정량취합매련반응(RT-PCR)검측hsa-miR-340재방광암T24세포중상대표체량,학정능구전염성공병유교고적전염솔후,분별통과사갑기우담서람(MTT)법화류식세포계수의,분석전염hsa-miR-340모의물전후대방광암T24세포적증식급조망능력적영향。결과①hsa-miR-340모의물가재방광암T24세포중표체,병이RT-PCR험증상대함량교고,차이유통계학의의(P<0.05)。②증식실험중분별재48h화72h시파실험조여음성대조조화공백대조조상대비,방광암T24세포생장증식명현수억제차차이유통계학의의(P<0.05),설명hsa-miR-340과표체후,능사T24세포증식능력수도유효억제。③hsa-miR-340모의물전염T24세포48h후,이류식세포의검측T24세포조망솔,분별위실험조(11.37±0.41)%、음성대조조(6.72±0.32)%、공백대조조(6.62±0.23)%,비교후차이유통계학의의(P<0.05),설명hsa-miR-340과표체사T24세포적조망현저증가。결론hsa-miR-340가능삼여방광암적진전。
Objective To investigate effects of upregulated hsa-miR-340 on the proliferation and apoptosis of bladder cancer T24 cells .Methods Hsa-miR-340 mimics were chemically synthetized and transiently transfect-ed into bladder cancer T24 cells .The expression of hsa-miR-340 in T24 cells was determined using quantitative polymerase chain reaction (RT-PCR) .Make sure that the T24 cells had been successfully transfected and on a high rate .Proliferation and apoptosis of the T24 cells were respectively evaluated using flow cytometry (FCM ) and MTT assay .Results ① The bladder cancer T24 cells could be transfected by hsa-miR-340 mimics and hsa-miR-340 quantification showed high expression in T24 cells (P<0.05) .②Compared with the control group and the blank group ,the experimental group could significantly inhibit proliferation of T 24 cells (P<0.05) .③In the FCM test ,we put each group into the flow cytometric and found that the apoptosis rates of the experimental group ,the control group and the blank group were (11.37 ± 0.41)% ,(6.72 ± 0.32)% and (6.62 ± 0.23)% ,re-spectively .The apoptosis of T24 cells was obviously increased (P<0.05) .Conclusion The relative high expres-sion of hsa-miR-340 may be involved in the progression of bladder cancer .