Department of Cellular and Molecular Medicine, George E. Palade Laboratories, University of California, San Diego School of Medicine, La Jolla, CA 92093-0651, USA.
FASEB J. 2011 Feb;25(2):590-9. doi: 10.1096/fj.10-167304. Epub 2010 Oct 25.
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.
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。