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首页> 外文期刊>Cancer: A Journal of the American Cancer Society >Characterization of the Roles of RHOC and RHOA GTPases in Invasion, Motility, and' Matrix Adhesion in Inflammatory and Aggressive Breast Cancers
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Characterization of the Roles of RHOC and RHOA GTPases in Invasion, Motility, and' Matrix Adhesion in Inflammatory and Aggressive Breast Cancers

机译:RHOC和RHOAGTpases在炎性和侵袭性乳腺癌中的侵袭,运动和“基质粘附”作用的表征。

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BACKGROUND: The 2 closely related small GTPases, RHOC and RHOA, are involved in mammary gland carcinogenesis; however, their specific roles in determining cancer cell adhesion and invasion have not been elucidated. METHODS: RHOA and RHOC are highly homologous, thereby posing a major challenge to study their individual functions in cancer cells. By selectively knocking down these proteins, we have been able to alternatively inhibit RHOC and RHOA, while preserving expression of the other rho protein. Quantitative analyses of the growth patterns and invasion in the aggressive estrogen receptor negative cell lines MDA-231 and SUM149 were carried out on collagen I and Matrigel substrates. RESULTS: RHOC, and not RHOA, modulates surface expression and colocalization of a2 and (31 integrins in MDA-MB-231 on collagen 1. Neither RHOC or RHOA affected integrin expression in the inflammatory breast cancer cell line SUM149, further highlighting the different regulation of adhesion and motility in inflammatory breast cancer. CONCLUSIONS: This work shows that RHOC and RHOA play different roles in cell-matrix adhesion, motility, and invasion of MDA-MB-231 and reaffirms the crucial role of RHOC-GTPase in inflammatory breast cancer cell invasion.
机译:背景:两个紧密相关的小GTP酶RHOC和RHOA与乳腺癌变有关。然而,尚未阐明它们在确定癌细胞粘附和侵袭中的特定作用。方法:RHOA和RHOC高度同源,因此对研究它们在癌细胞中的功能提出了重大挑战。通过选择性地敲低这些蛋白,我们能够选择性地抑制RHOC和RHOA,同时保留其他rho蛋白的表达。在胶原蛋白I和基质胶基质上对侵袭性雌激素受体阴性细胞系MDA-231和SUM149的生长模式和侵袭进行了定量分析。结果:RHOC,而不是RHOA,调节胶原蛋白1的MDA-MB-231中a2和(31个整联蛋白的表面表达和共定位。RHOC或RHOA均不影响炎症性乳腺癌细胞SUM149中整联蛋白的表达,进一步强调了不同的调节结论:这项工作表明RHOC和RHOA在细胞基质粘附,运动和MDA-MB-231的侵袭中发挥不同的作用,并重申了RHOC-GTPase在炎性乳腺癌中的关键作用细胞入侵。

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