Sun De-Cong, Shi Yan, Wang Ling-Xiong, Lv Yao, Han Quan-Li, Wang Zhi-Kuan, Dai Guang-Hai
The Second Department of Oncology, Chinese PLA General Hospital, Beijing, China.
Current Adress: Cancer Center Key Laboratory, Chinese PLA General Hospital, Beijing, China.
Oncotarget. 2017 Mar 16;8(39):66550-66558. doi: 10.18632/oncotarget.16289. eCollection 2017 Sep 12.
Leucine-rich alpha-2-glycoprotein-1 (encoded by ) has been shown to be involved in multiple cancer progression and angiogenesis. LRG1 has been shown to be one of the five plasma proteins that can be used for colorectal cancer (CRC) diagnosis. The objective of the current study was to explore relationship between LRG1 protein expression and microvessel density (MVD) in stage III CRC.
A single-center retrospective analysis of all stage III CRC who underwent surgery and adjuvant chemotherapy was carried out. LRG1 and CD34 were tested in tumor tissues by immunohistochemistry (IHC).
LRG1 protein expression was significantly associated with MVD ( <0.001) and other clinicopathological parameters, including T stage (=0.028), differentiation (=0.035) and vascular invasion (=0.007). Cox multivariate regression analysis showed that LRG1 protein expression was an independent poor predictive factor for both disease-free and overall survival.
LRG1 protein expression can be used as a prognostic marker for stage III CRC along with its use as a diagnostic marker for CRC in general.
富含亮氨酸的α-2-糖蛋白-1(由[此处基因名称缺失]编码)已被证明参与多种癌症进展和血管生成。LRG1已被证明是可用于结直肠癌(CRC)诊断的五种血浆蛋白之一。本研究的目的是探讨III期CRC中LRG1蛋白表达与微血管密度(MVD)之间的关系。
对所有接受手术和辅助化疗的III期CRC患者进行单中心回顾性分析。通过免疫组织化学(IHC)检测肿瘤组织中的LRG1和CD34。
LRG1蛋白表达与MVD显著相关(<0.001),并与其他临床病理参数相关,包括T分期(=0.028)、分化程度(=0.035)和血管侵犯(=0.007)。Cox多因素回归分析表明,LRG1蛋白表达是无病生存期和总生存期的独立不良预测因素。
LRG1蛋白表达不仅可作为CRC的一般诊断标志物,还可作为III期CRC的预后标志物。