Gómez del Pulgar Teresa, Bandrés Eva, Espina Carolina, Valdés-Mora Fátima, Pérez-Palacios Rosa, García-Amigot Fermín, García-Foncillas Jesús, Lacal Juan Carlos
Translational Oncology Unit CSIC-UAM-La Paz, Centro Nacional de Biotecnología, Madrid, Spain.
Int J Biochem Cell Biol. 2007;39(12):2289-302. doi: 10.1016/j.biocel.2007.06.014. Epub 2007 Jul 4.
The small GTPase Rac1 is involved in the regulation of critical cellular functions, such as transcription control, cell cycle, and organization of actin cytoskeleton. Rac1 signalling modulates cancer progression since its overexpression leads to an increased tumour growth of xenografts of human colorectal tumour cells, while a drastic reduction of Rac1 expression by siRNA interferes with cancer progression (Espina et al., unpublished results). We aimed to study the molecular basis for the specific contribution of Rac1 in the progression of colorectal cancer. Comparative microarray analysis of a human colorectal carcinoma cell line genetically engineered to display different levels of Rac1 identified novel target genes for this GTPase. These results suggest that Rac1 plays a critical role in signalling transduction pathways relevant to human colorectal tumour progression, such as activation of Wnt signalling, inhibition of TGF-beta signalling, and enhancement of metastasis-inducing genes.
小GTP酶Rac1参与关键细胞功能的调节,如转录控制、细胞周期以及肌动蛋白细胞骨架的组织。Rac1信号传导调节癌症进展,因为其过表达导致人结肠肿瘤细胞异种移植瘤的肿瘤生长增加,而通过siRNA大幅降低Rac1表达则会干扰癌症进展(埃斯皮纳等人,未发表结果)。我们旨在研究Rac1在结直肠癌进展中特定作用的分子基础。对经过基因工程改造以显示不同水平Rac1的人结肠癌细胞系进行比较微阵列分析,确定了这种GTP酶的新靶基因。这些结果表明,Rac1在与人类结肠肿瘤进展相关的信号转导途径中起关键作用,如Wnt信号的激活、TGF-β信号的抑制以及转移诱导基因的增强。