Department of Pathology, Dadong District, Affiliated Cancer Hospital of Dalian University of Technology (Liaoning Cancer Hospital and Institute, Cancer Hospital of China Medical University), No. 44 of Xiaoheyan Road, Shenyang, 110042, China.
BMC Cancer. 2023 Jun 5;23(1):507. doi: 10.1186/s12885-023-11011-0.
A significant proportion of patients can not benefit from neoadjuvant chemotherapy (NCT) due to drug resistance. Cancer-associated fibroblasts (CAFs) influence many biological behaviours of tumors, including chemo-resistance. This study aims to explore whether CAFs expressing FAP, CD10, and GPR77 affect the efficacy of NCT and the prognosis of patients with gastric cancer, and its mechanism.
One hundred seventy-one patients with locally progressive gastric adenocarcinoma who had undergone NCT and radical surgery were collected. Immunohistochemistry was used to detect the expression of FAP, CD10, and GPR77 in CAFs; the EMT markers (N-cadherin, Snail1, and Twist1) and the CSC markers (ALDH1, CD44, and LGR5) in gastric cancer cells. The χ test was used to analyze the relationship between the expression of CAF, EMT, and CSC markers and the clinicopathological factors, as well as the relationship between CAF markers and EMT, and CSC markers. Logistic regression and Cox risk regression were used to analyze the relationship between the expression of CAF, EMT, and CSC markers and TRG grading and OS; Kaplan-Meier analysis was used for survival analysis and plotting the curves.
The expression of CAF markers FAP, CD10, and GPR77 was closely associated with that of EMT markers; FAP and CD10 were closely related to CSC markers. In the univariate analysis of pathological response, CAF markers (FAP, CD10, GPR77), EMT markers (N-cadherin, Snail1, Twist1), and CSC markers (ALDH1, LGR5, CD44), were all closely associated with pathological response (all p < 0.05). Only Twist1 was an independent factor affecting pathological response in multifactorial analysis (p = 0.001). In a univariate analysis of OS, expression of FAP and CD10 in CAF, as well as expression of EMT biomarkers (N-cadherin, Snail1), were significant factors influencing patient prognosis (all p < 0.05). Multifactorial analysis revealed N-cadherin (p = 0.032) and Snail1 (p = 0.028), as independent prognostic factors affecting OS.
FAP, CD10, and GPR77 labeled CAF subgroup may lead to NCT resistance and poor prognosis by inducing EMT and CSC of gastric cancer cells in locally advanced gastric cancer patients.
由于耐药性,相当一部分患者无法从新辅助化疗(NCT)中获益。癌相关成纤维细胞(CAFs)影响肿瘤的许多生物学行为,包括化疗耐药性。本研究旨在探讨表达 FAP、CD10 和 GPR77 的 CAFs 是否影响胃癌患者 NCT 的疗效和预后及其机制。
收集 171 例局部进展期胃腺癌患者,均行 NCT 及根治性手术。采用免疫组织化学法检测 CAFs 中 FAP、CD10 和 GPR77 的表达;检测胃癌细胞中 EMT 标志物(N-钙黏蛋白、Snail1 和 Twist1)和 CSC 标志物(ALDH1、CD44 和 LGR5)。卡方检验分析 CAF、EMT 和 CSC 标志物的表达与临床病理因素的关系,以及 CAF 标志物与 EMT 和 CSC 标志物的关系。采用 logistic 回归和 Cox 风险回归分析 CAF、EMT 和 CSC 标志物的表达与 TRG 分级和 OS 的关系;采用 Kaplan-Meier 分析进行生存分析并绘制曲线。
CAF 标志物 FAP、CD10 和 GPR77 的表达与 EMT 标志物密切相关;FAP 和 CD10 与 CSC 标志物密切相关。在病理反应的单因素分析中,CAF 标志物(FAP、CD10、GPR77)、EMT 标志物(N-钙黏蛋白、Snail1、Twist1)和 CSC 标志物(ALDH1、LGR5、CD44)均与病理反应密切相关(均 p<0.05)。多因素分析仅发现 Twist1 是影响病理反应的独立因素(p=0.001)。在 OS 的单因素分析中,CAF 中 FAP 和 CD10 的表达以及 EMT 生物标志物(N-钙黏蛋白、Snail1)的表达是影响患者预后的显著因素(均 p<0.05)。多因素分析显示 N-钙黏蛋白(p=0.032)和 Snail1(p=0.028)是影响 OS 的独立预后因素。
在局部进展期胃癌患者中,FAP、CD10 和 GPR77 标记的 CAF 亚群可能通过诱导胃癌细胞 EMT 和 CSC 导致 NCT 耐药和预后不良。