首页> 美国卫生研究院文献>Journal of Experimental Clinical Cancer Research : CR >Correction to: Short hairpin RNA- mediated gene knockdown of FOXM1 inhibits the proliferation and metastasis of human colon cancer cells through reversal of epithelial-to-mesenchymal transformation
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Correction to: Short hairpin RNA- mediated gene knockdown of FOXM1 inhibits the proliferation and metastasis of human colon cancer cells through reversal of epithelial-to-mesenchymal transformation

机译:校正至:短发夹RNA介导的FOXM1的基因敲低通过上皮对间充质转化的逆转抑制人结肠癌细胞的增殖和转移

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摘要

Effect of altered FOXM1 expression on colorectal cancer cell migration and invasion in vitro. a: Wound healing assays were carried out at 24 h after transfection in 24-well plates, when cell confluence rate reached above 90% and a linear wound across the monolayer was done. The wound gap was photographed every 24 h, the gap width was measured (μm) using Open Lab software. b: The wound rate was calculated and displayed graphically as described in the Materials and Methods. c-d: SW620 cells of three groups were digested and resuspended in serum-free culture medium and allowed to migrate toward the lower chamber with coated or uncoated matrigel for 24 h. Invading cells were stained with 0.1% crystal violet and counted manually. C-Left: transwell migration assay, Right: transwell invasion assay. d: The number of invading SW620 cells by cell migration (upper) and invasion (lower) assay was counted manually. Each experiment was repeated thrice independently. Scale bar = 200 μm in those figures
机译:改变FoxM1表达对成直肠癌细胞迁移和体外侵袭的影响。答:在24孔板转染后24小时在24孔板中进行伤口愈合测定,当达到90%以上的电池汇合率并进行整体层穿过单层的线性突起后。每24小时拍摄伤口间隙,使用开放式实验室软件测量间隙宽度(μm)。 B:如材料和方法中所述计算伤口率并以图形方式显示。 C-D:在无血清培养基中消化并重新悬浮三组的SW620细胞,并迁移到下腔室,涂覆或未涂覆的Matrigel 24小时。入侵细胞用0.1%晶体紫色染色并手动计数。 C左:Transwell迁移测定,右:Transwell入侵测定。 D:手动计算通过细胞迁移(上)和侵袭(上)测定的侵入SW620细胞的数量。每个实验都独立地重复。这些数字中的秤条=200μm

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