Department of General Surgery, Affiliated Anhui Provincial Hospital, Hefei, Anhui, China.
Anhui Province Key Laboratory of Hepatopancreatobiliary Surgery, Hefei, Anhui, China.
Cancer Biomark. 2018;23(3):353-361. doi: 10.3233/CBM-181358.
Free fatty acid receptor 4 (FFAR4) is associated with the epithelial mesenchymal transition (EMT) and is involved in the progression of several types of cancer. However, the role of FFAR4 in cholangiocarcinoma (CCA) remains unclear.
The present study evaluated the diagnosis and prognosis of CCA using FFAR4 as a biomarker.
Immunohistochemistry was employed to detect expression of FFAR4 in 98 samples of CCA tissues and adjacent tissues. In addition, expression of E-cadherin, vimentin, Snail-1, CK7 and CK19 in the 98 samples of CCA tissues was detected, and relationships with FFAR4 were analyzed. Correlation between FFAR4 and clinical pathological factors and prognosis was also analyzed.
FFAR4 was highly expressed in 72.4% (71/98) of CCA tissues and 29.6% (29/98) of adjacent tissues, with a statistically significant difference between the two tissue types (P< 0.05). A negative correlation between high expression FFAR4 and E-cadherin expression in CCA tissues was also observed (r=-0.445, P< 0.001), and high expression of FFAR4 was positively correlated with vimentin (r= 0.354, P< 0.001), Snail-1(r= 0.496, P< 0.001), CK7(r= 0.494, P< 0.001) and CK19 (r= 0.532, P< 0.001). Moreover, the degree of FFAR4 expression was associated with aggressive clinicopathological characteristics, such as histological grade, perineural invasion (PNI), lymph node metastasis (LNM), advanced TNM stage and preoperative serum CA19-9 level (P< 0.05). In terms of prognosis, CCA patients with high FFAR4 expression showed shorter disease-free survival (DFS) (P< 0.05) and overall survival (OS) (P< 0.05) than did patients with low FFAR4 expression.
FFAR4 overexpression may mediate the process of CCA EMT. In addition, FFAR4 is promising as a new diagnostic molecule and therapeutic target for CCA.
游离脂肪酸受体 4(FFAR4)与上皮间质转化(EMT)有关,并且参与了多种类型癌症的进展。然而,FFAR4 在胆管癌(CCA)中的作用尚不清楚。
本研究使用 FFAR4 作为生物标志物来评估 CCA 的诊断和预后。
采用免疫组织化学法检测 98 例 CCA 组织及其相邻组织中 FFAR4 的表达情况。此外,检测 98 例 CCA 组织中 E-钙黏蛋白、波形蛋白、Snail-1、CK7 和 CK19 的表达情况,并分析与 FFAR4 的关系。还分析了 FFAR4 与临床病理因素和预后的相关性。
FFAR4 在 72.4%(71/98)的 CCA 组织和 29.6%(29/98)的相邻组织中高表达,两种组织类型之间存在统计学差异(P<0.05)。还观察到 CCA 组织中高表达 FFAR4 与 E-钙黏蛋白表达呈负相关(r=-0.445,P<0.001),并且高表达 FFAR4 与波形蛋白(r=0.354,P<0.001)、Snail-1(r=0.496,P<0.001)、CK7(r=0.494,P<0.001)和 CK19(r=0.532,P<0.001)呈正相关。此外,FFAR4 表达程度与侵袭性临床病理特征相关,如组织学分级、神经周围侵犯(PNI)、淋巴结转移(LNM)、晚期 TNM 分期和术前血清 CA19-9 水平(P<0.05)。就预后而言,高 FFAR4 表达的 CCA 患者无疾病生存(DFS)(P<0.05)和总生存(OS)(P<0.05)均短于低 FFAR4 表达的患者。
FFAR4 过表达可能介导 CCA EMT 的过程。此外,FFAR4 有望成为 CCA 的一种新的诊断分子和治疗靶点。