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D4-GDI是一种Rho GTP酶调节剂,可促进乳腺癌细胞的侵袭性。

D4-GDI, a Rho GTPase regulator, promotes breast cancer cell invasiveness.

作者信息

Zhang Yaqin, Zhang Baolin

机构信息

Division of Therapeutic Proteins, Office of Biotechnology Products, Center for Drug Evaluation and Research, Food and Drug Administration, Bethesda, Maryland, USA.

出版信息

Cancer Res. 2006 Jun 1;66(11):5592-8. doi: 10.1158/0008-5472.CAN-05-4004.

Abstract

D4-GDI is a Rho GDP dissociation inhibitor that is widely expressed in hematopoietic cells. Its possible expression and function in breast cancer cells has not been described. Here, we found that D4-GDI is expressed in a panel of breast cancer cell lines, but not in benign-derived mammary epithelial cells. Knockdown of D4-GDI expression in MDA-MB-231 cells by RNA interference blocks cell motility and invasion. The cells lacking D4-GDI grown on Matrigel revert to a normal breast epithelial phenotype characterized by the formation of cavitary structures. Silencing D4-GDI expression inhibits beta1-integrin expression and cell-matrix adhesion. Reintroduction of D4-GDI fully restored both beta1-integrin expression and cellular invasion. Knockdown of D4-GDI in BT549 cells results in a similar effect. These results show that D4-GDI modulates breast cancer cell invasive activities.

摘要

D4-GDI是一种Rho GDP解离抑制剂,在造血细胞中广泛表达。其在乳腺癌细胞中的可能表达及功能尚未见报道。在此,我们发现D4-GDI在一组乳腺癌细胞系中表达,但在良性来源的乳腺上皮细胞中不表达。通过RNA干扰敲低MDA-MB-231细胞中D4-GDI的表达可阻断细胞迁移和侵袭。在基质胶上生长的缺乏D4-GDI的细胞恢复为以形成空泡状结构为特征的正常乳腺上皮表型。沉默D4-GDI表达可抑制β1整合素表达及细胞与基质的黏附。重新引入D4-GDI可完全恢复β1整合素表达及细胞侵袭能力。在BT549细胞中敲低D4-GDI也产生类似效果。这些结果表明D4-GDI可调节乳腺癌细胞的侵袭活性。

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