中华实验外科杂志
中華實驗外科雜誌
중화실험외과잡지
CHINESE JOURNAL OF EXPERIMENTAL SURGERY
2014年
9期
1954-1956
,共3页
孙烈%陈国卫%尹杰%朱静%田孝东%杨尹默%万远廉%刘玉村
孫烈%陳國衛%尹傑%硃靜%田孝東%楊尹默%萬遠廉%劉玉村
손렬%진국위%윤걸%주정%전효동%양윤묵%만원렴%류옥촌
富含半胱氨酸的酸性分泌蛋白%细胞外基质%胰腺癌
富含半胱氨痠的痠性分泌蛋白%細胞外基質%胰腺癌
부함반광안산적산성분비단백%세포외기질%이선암
Secreted protein acidic and rich in cysteine%Extrcelluar matrix%Pancreatic cancer
目的 观察外源性富含半胱氨酸的酸性分泌蛋白(SPARC)对胰腺癌细胞增殖、迁移和侵袭力等生物学行为的影响.方法 将胰腺癌细胞Mia PaCa-2和PANC-1中加入不同浓度的外源性SPARC(0、0.5、1.0、3.0、5.0、10.0 mg/L)作为实验组,以空白组作对照,采用噻唑蓝(MTT)实验分析胰腺癌细胞增殖能力的变化;将胰腺癌细胞Mia PaCa-2和PANC-1中加入5 mg/L外源性SPARC,以空白组为对照,培养24 h,采用单个细胞移动实验分析胰腺癌细胞迁移能力的变化,采用Matrigel侵袭力实验分析胰腺癌细胞侵袭能力的变化.结果 外源性SPARC能够抑制胰腺癌细胞的增殖,且抑制作用具有浓度依赖性,10.0 mg/L外源性SPARC可使Mia PaCa-2和PANC-1细胞的增殖能力分别下降(32.8±7.4)%和(32.5±1.8)%.5.0 mg/L外源性SPARC能够使Mia PaCa-2和PANC-1细胞在24 h的移动距离分别下降26%和39%,细胞侵袭转移数目分别下降30%和56%.结论 外源性SPARC可抑制胰腺癌细胞的增殖、迁移和侵袭能力,细胞外基质成分对恶性肿瘤的生物学行为可产生影响.
目的 觀察外源性富含半胱氨痠的痠性分泌蛋白(SPARC)對胰腺癌細胞增殖、遷移和侵襲力等生物學行為的影響.方法 將胰腺癌細胞Mia PaCa-2和PANC-1中加入不同濃度的外源性SPARC(0、0.5、1.0、3.0、5.0、10.0 mg/L)作為實驗組,以空白組作對照,採用噻唑藍(MTT)實驗分析胰腺癌細胞增殖能力的變化;將胰腺癌細胞Mia PaCa-2和PANC-1中加入5 mg/L外源性SPARC,以空白組為對照,培養24 h,採用單箇細胞移動實驗分析胰腺癌細胞遷移能力的變化,採用Matrigel侵襲力實驗分析胰腺癌細胞侵襲能力的變化.結果 外源性SPARC能夠抑製胰腺癌細胞的增殖,且抑製作用具有濃度依賴性,10.0 mg/L外源性SPARC可使Mia PaCa-2和PANC-1細胞的增殖能力分彆下降(32.8±7.4)%和(32.5±1.8)%.5.0 mg/L外源性SPARC能夠使Mia PaCa-2和PANC-1細胞在24 h的移動距離分彆下降26%和39%,細胞侵襲轉移數目分彆下降30%和56%.結論 外源性SPARC可抑製胰腺癌細胞的增殖、遷移和侵襲能力,細胞外基質成分對噁性腫瘤的生物學行為可產生影響.
목적 관찰외원성부함반광안산적산성분비단백(SPARC)대이선암세포증식、천이화침습력등생물학행위적영향.방법 장이선암세포Mia PaCa-2화PANC-1중가입불동농도적외원성SPARC(0、0.5、1.0、3.0、5.0、10.0 mg/L)작위실험조,이공백조작대조,채용새서람(MTT)실험분석이선암세포증식능력적변화;장이선암세포Mia PaCa-2화PANC-1중가입5 mg/L외원성SPARC,이공백조위대조,배양24 h,채용단개세포이동실험분석이선암세포천이능력적변화,채용Matrigel침습력실험분석이선암세포침습능력적변화.결과 외원성SPARC능구억제이선암세포적증식,차억제작용구유농도의뢰성,10.0 mg/L외원성SPARC가사Mia PaCa-2화PANC-1세포적증식능력분별하강(32.8±7.4)%화(32.5±1.8)%.5.0 mg/L외원성SPARC능구사Mia PaCa-2화PANC-1세포재24 h적이동거리분별하강26%화39%,세포침습전이수목분별하강30%화56%.결론 외원성SPARC가억제이선암세포적증식、천이화침습능력,세포외기질성분대악성종류적생물학행위가산생영향.
Objective To investigate the effects of exogenous secreted protein acidic and rich in cysteine (SPARC) on proliferation,migration and invasion ability of human pancreatic cancer cell lines.Methods The cuhured Mia PaCa-2 and PANC-1 pancreatic cancer cells were established in the presence of different concentrations (0,0.5,1.0,3.0,5.0,10.0 mg/L) or absence of exogenous SPARC as experimental and control groups.The change of proliferation was measured by methyl thiazol tetrazolium (MTT) assay.The 24 h cultured Mia PaCa-2 and PANC-1 pancreatic cancer cells were established in the presence (5 mg/L) or absence of exogenous SPARC as experimental and control groups,and the change of migration ability was detected by single cell migration assay and the change of invasion ability by Matrigel invasion assay respectively.Results Exogenous SPARC could inhibit the proliferation of cells in a concentration-dependent manner.Cell proliferation was inhibited in the presence of 10.0 mg/L exogenous SPARC by (32.8 ± 7.4) % and (32.5 ± 1.8) % in Mia PaCa-2 and PANC-1,respectively.5.0 mg/L SPARC reduced the distance covered within 24 h by 26% and 39%,and in the presence of 5.0 mg/L SPARC the number of invasive cells was inhibited by 30% and 56% in 24 h,respectively.Conclusion Exogenous SPARC could inhibit the proliferation,migration and invasion ability in pancreatic cancer cells,suggesting extracelluar matrix may affect biological functions of malignant tumors.