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GIV/Girdin 表达,一种转移相关蛋白,预测结肠癌患者的生存。

Expression of GIV/Girdin, a metastasis-related protein, predicts patient survival in colon cancer.

机构信息

Department of Cellular and Molecular Medicine, George E. Palade Laboratories, University of California, San Diego School of Medicine, La Jolla, CA 92093-0651, USA.

出版信息

FASEB J. 2011 Feb;25(2):590-9. doi: 10.1096/fj.10-167304. Epub 2010 Oct 25.

Abstract

Metastasis accounts for the majority of cancer-related deaths. Accurate prediction of metastatic potential of tumors has been elusive, and the search for clinically useful markers continues. We previously reported that GIV/Girdin triggers tumor cell migration by virtue of a C-terminal guanine-nucleotide exchange factor motif that activates Gαi. Here we identify GIV as a metastasis-related protein whose full-length transcript (GIV-fl) is expressed exclusively in highly invasive colon, breast, and pancreatic carcinoma cells and not in their poorly invasive counterparts. A prospective, exploratory biomarker study conducted on a cohort of 56 patients with stage II colorectal cancer revealed a significant correlation between GIV-fl expression in tumor epithelium and shortened metastasis-free survival. Survival rate for patients with GIV-fl-positive tumors is significantly reduced compared with the patients with GIV-fl-negative tumors [P<0.0001; hazard ratio=0.076; CI=0.052-0.30 (95%)]. At the 5-yr mark, survival is 100% in the GIV-fl-negative group and 62 ± 9% (mean±SE; P=6×10(-5)) in the GIV-fl-positive group. Furthermore, GIV-fl expression predicts a risk of mortality independent of the microsatellite stability status, a well-established prognosticator of colorectal cancers. We conclude that GIV-fl is a novel metastasis-related protein and an independent adverse prognosticator that may serve as a useful adjunct to traditional staging strategies in colorectal carcinoma.

摘要

转移是癌症相关死亡的主要原因。准确预测肿瘤的转移潜力一直难以实现,因此仍在继续寻找临床有用的标志物。我们之前报道过,GIV/Girdin 通过其 C 末端鸟嘌呤核苷酸交换因子基序触发肿瘤细胞迁移,该基序激活 Gαi。在这里,我们确定 GIV 是一种与转移相关的蛋白质,其全长转录本(GIV-fl)仅在高度侵袭性的结肠、乳腺和胰腺癌细胞中表达,而不在其侵袭性较低的对应物中表达。对 56 名 II 期结直肠癌患者进行的一项前瞻性探索性生物标志物研究表明,肿瘤上皮中的 GIV-fl 表达与无转移生存时间缩短之间存在显著相关性。与 GIV-fl 阴性肿瘤患者相比,GIV-fl 阳性肿瘤患者的生存率显著降低[P<0.0001;风险比=0.076;CI=0.052-0.30(95%)]。在 5 年标记时,GIV-fl 阴性组的生存率为 100%,GIV-fl 阳性组为 62±9%(平均值±SE;P=6×10(-5))。此外,GIV-fl 表达可预测死亡率风险,独立于微卫星不稳定性状态,这是结直肠癌的一种既定预后因素。我们得出的结论是,GIV-fl 是一种新的与转移相关的蛋白质和独立的预后不良因素,它可能成为结直肠癌传统分期策略的有用辅助手段。

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