Gao Hongyu, Yao Qiang, Lan Xiuwen, Li Sen, Wu Junlong, Zeng Guangchun, Xue Yingwei
Department of Gastroenterologic Surgery.
Department of Pathology, The Affiliated Tumor Hospital, Harbin Medical University, Harbin, People's Republic of China.
Onco Targets Ther. 2016 Oct 31;9:6711-6718. doi: 10.2147/OTT.S114756. eCollection 2016.
Hyaluronic acid-binding protein 1 (HABP1/gC1qR/p32) has been recently implicated in oncogenesis and cancer progression in various malignancies; however, its clinical role in gastric cancer (GC) is still unclear.
First, HABP1 expression was determined by Western blot analysis and immunohistochemistry. Then, we evaluated the expression of HABP1 and its clinical significance in tumor tissues from 181 patients with GC.
Expression of HABP1 protein in GC tissues was noticeably higher than that in adjacent nonneoplastic tissues (=0.018). Increased HABP1 expression was significantly associated with tumor, node, and metastasis (TNM) stage (=0.006), depth of invasion (=0.001), lymph node metastasis (=0.001), liver metastasis (=0.024), and peritoneum metastasis (=0.009). Patients with high expression of HABP1 had poor overall survival rate (<0.001). In addition, histologic grade (=0.017), TNM stage (<0.001), Borrmann grouping (<0.001), depth of invasion (<0.001), lymph node metastasis (<0.001), liver metastasis (=0.010), and tumor size (<0.001) were independent prognostic factors for overall survival. Multivariate Cox regression analysis revealed that HABP1 (=0.004), histologic grade (=0.047), TNM stage (<0.001), Borrmann grouping (<0.001), and liver metastasis (=0.038) were independent factors for overall survival in patients with GC.
These findings demonstrated that HABP1 was an indicator for GC progression and poor survival, which highlighted its potential role as a therapeutic target for GCs.
透明质酸结合蛋白1(HABP1/gC1qR/p32)最近被认为与多种恶性肿瘤的肿瘤发生和癌症进展有关;然而,其在胃癌(GC)中的临床作用仍不清楚。
首先,通过蛋白质印迹分析和免疫组织化学确定HABP1的表达。然后,我们评估了181例GC患者肿瘤组织中HABP1的表达及其临床意义。
GC组织中HABP1蛋白的表达明显高于相邻的非肿瘤组织(=0.018)。HABP1表达增加与肿瘤、淋巴结和转移(TNM)分期(=0.006)、浸润深度(=0.001)、淋巴结转移(=0.001)、肝转移(=0.024)和腹膜转移(=0.009)显著相关。HABP1高表达的患者总生存率较差(<0.001)。此外,组织学分级(=0.017)、TNM分期(<0.001)、Borrmann分型(<0.001)、浸润深度(<0.001)、淋巴结转移(<0.001)、肝转移(=0.010)和肿瘤大小(<0.001)是总生存的独立预后因素。多变量Cox回归分析显示,HABP1(=0.004)、组织学分级(=0.047)、TNM分期(<0.001)、Borrmann分型(<0.001)和肝转移(=0.038)是GC患者总生存的独立因素。
这些发现表明,HABP1是GC进展和不良生存的指标,突出了其作为GC治疗靶点的潜在作用。