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作 者:潘兵[1] 路璐[1] 陈仲[1] 顾金龙[1] 赵明辉[1] 张春明[1] 韩佩珍[1]
机构地区:[1]中国医学科学院中国协和医科大学放射医学研究所,天津300192
出 处:《中国肿瘤生物治疗杂志》2007年第2期115-119,共5页Chinese Journal of Cancer Biotherapy
基 金:国家自然科学基金资助项目(No.30500135)
摘 要:目的:研究人脂联素重组体对人乳腺癌MDA-MB-231细胞体外侵袭能力的影响。方法:将MDA-MB-231细胞分设对照组和脂联素重组体加药(2.5、5.0、10、20、30μg/ml)组,药物作用一定时间后,分别以MTT法、Transwell小室实验,Chamber小室实验,黏附实验检测脂联素重组体对乳腺癌细胞增殖、侵袭、迁移和黏附能力的影响,以明胶酶谱法检测其对肿瘤细胞分泌MMP-2和MMP-9的影响。结果:脂联素重组体质量浓度高于5.0μg/ml时,对MDA-MB-231细胞生长具有明显的抑制作用(P<0.01);能明显地降低肿瘤细胞体外侵袭能力(P<0.01),侵袭抑制率随脂联素重组体质量浓度的升高而增加,介于22.64%~77.84%之间;脂联素重组体质量浓度高于2.5μg/ml时,明显地抑制肿瘤细胞的迁移能力(P<0.01);脂联素重组体对ECM和FN黏附能力影响的程度不同,对FN的敏感性大于ECM;脂联素重组体质量浓度大于2.5μg/ml时,明显抑制肿瘤细胞MMP-2和MMP-9的分泌(P<0.05或P<0.01),后者的分泌量随质量浓度的升高而下降。结论:脂联素重组体在大于2·5μg/ml时,可能通过保护基底膜不受破坏而抑制人乳腺癌细胞的侵袭能力。Objective: To investigate the effects of recombinant adiponectin (RA) on the invasive ability of human breast cancer cell line MDA-MB-231. Methods: MDA-MB-231 cells were divided into control group and RA(2.5, 5.0, 10, 20, and 30 μg/ml) treatment groups. The effect of RA on proliferation of MDA-MB-231 cells was measured by MrlT assay; the invasive and migration abilities of MDA-MB-231 cell were assayed in Transwell cell culture chamber; cell adhesion assay was carried out in a microcuhure well precoated with fibronectin. Gelatinolytic activities of both MMP-2 and MMP-9 secreted by cancer cells were measured by zymogrophy analysis. Results : The growth and invasive ability of MDA- MB-231 cells were obviously inhibited when the concentration of RA was higher than 5.0 μg/ml ( P 〈 0.01 ) ; the inhibition of migration was in a concentration-dependent manner, with the inhibitory rate ranging from 22.64%-77.84%. When the concentration of RA was higher than 2.5 μg/ml, the migration of tumor and the secretion of MMP-2 and MMP-9 were obviously inhibited (P 〈0.05 ,P 〈0.01 ) ; the secretion of MMP-9 decreased with the increase of RA concentration. RA was more sensitive to FN and than to ECM. Conclusion: These results indicate that adiponectin is effective in suppressing tumor cell invasion when its concentration is 〉 2.5 μg/ml ; the mechanism might be the down-regulation of MMPs.
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