Xi Yu-Ning, Xue Jun, Wu Xue-Liang, Qu Ming, Sun Guang-Yuan, Han Lei, Guo Fei, Zhang Chun-Ze, Wang Yi-Fei, Liang Wei-Zheng
Department of General Surgery, The First Affiliated Hospital of Hebei North University, Zhangjiakou, Hebei 075000,China.
Institute of Tumor, The First Affiliated Hospital of Hebei North University, Zhangjiakou, Hebei 075000,China.
Zhongguo Yi Xue Ke Xue Yuan Xue Bao. 2024 Aug;46(4):528-538. doi: 10.3881/j.issn.1000-503X.15899.
Objective To analyze the sensitivity of ARHGAP8 in predicting the efficacy of neoadjuvant chemotherapy in the patients with locally advanced mid-low colorectal cancer and provide accurate evidence for the treatment of advanced colorectal cancer. Methods The differentially expressed gene ARHGAP8 was screened out by bioinformatics analysis.Cancer tissue and rectal tissue of 68 patients with primary rectal cancer were selected.The rectal cancer tissue samples and the rectal tissue samples were collected for clinical validation of ARHGAP8 expression by quantitative real-time PCR,Western blotting,and immunohistochemistry.The clinical and pathological features such as gender,age,tumor stage,differentiation degree,and pathological type of the patients were collected for functional validation.Forty-four patients with locally advanced mid-low rectal cancer who received neoadjuvant chemotherapy were selected for immunohistochemical examination of ARHGAP8 expression.The expression level of ARHGAP8 was compared between before and after chemotherapy and among different efficacy groups. Results The bioinformatics analysis revealed differences in the expression level of ARHGAP8 between the cancer tissue and rectal tissue (<0.001).The expression level of ARHGAP8 was correlated with tumor stage (=0.024),lymph node metastasis (=0.007),and age (=0.005).Quantitative real-time PCR results showed that the mRNA level of ARHGAP8 in the cancer tissue was higher than that in the rectal tissue (<0.001).Western blotting and immunohistochemistry results demonstrated that the protein level of ARHGAP8 in the cancer tissue was higher than that in the rectal tissue (=0.011).The expression of ARHGAP8 was correlated with tumor size (=0.010) and pathological stage (=0.005),while it showed no significant association with tumor differentiation degree,lymph node metastasis,liver metastasis,Ki-67,or microsatellite instability expression level.The 44 patients receiving neoadjuvant chemotherapy included 13,8,8,and 15 patients of tumor regression grades 0,1,2,and 3,respectively.Among them,65.91% (29/44) patients showed responses to the treatment.After neoadjuvant chemotherapy,the expression of ARHGAP8 in the cancer tissue was down-regulated in the patients who responded to the chemotherapy (<0.001).The response rate in the patients with low protein level of ARHGAP8 was 92.86%,which was higher than that (53.33%) in the patients with high protein level of ARHGAP8 (=0.033). Conclusion ARHGAP8 is highly expressed in the rectal cancer tissue.The patients with locally advanced mid-low rectal cancer and low ARHGAP8 expression are more sensitive to neoadjuvant chemotherapy with the XELOX protocol.ARHGAP8 can serve as a potential biomarker for the occurrence and development of rectal cancer and an important index for evaluating the efficacy of neoadjuvant chemotherapy with the XELOX protocol in the patients with locally advanced mid-low rectal cancer.
目的 分析ARHGAP8在预测局部进展期结直肠癌患者新辅助化疗疗效中的敏感性,为晚期结直肠癌的治疗提供准确依据。方法 通过生物信息学分析筛选出差异表达基因ARHGAP8。选取68例原发性直肠癌患者的癌组织和直肠组织。收集直肠癌组织样本和直肠组织样本,采用定量实时荧光定量PCR、蛋白质印迹法及免疫组织化学法对ARHGAP8表达进行临床验证。收集患者的性别、年龄、肿瘤分期、分化程度及病理类型等临床病理特征进行功能验证。选取44例接受新辅助化疗的局部进展期低位直肠癌患者进行ARHGAP8表达的免疫组织化学检测。比较化疗前后及不同疗效组间ARHGAP8的表达水平。结果 生物信息学分析显示癌组织与直肠组织中ARHGAP8表达水平存在差异(<0.001)。ARHGAP8表达水平与肿瘤分期(=0.024)、淋巴结转移(=0.007)及年龄(=0.005)相关。定量实时荧光定量PCR结果显示癌组织中ARHGAP8的mRNA水平高于直肠组织(<0.001)。蛋白质印迹法及免疫组织化学结果表明癌组织中ARHGAP8的蛋白水平高于直肠组织(=0.011)。ARHGAP8的表达与肿瘤大小(=0.010)及病理分期(=0.005)相关,而与肿瘤分化程度、淋巴结转移、肝转移、Ki-67或微卫星不稳定性表达水平无显著关联。44例接受新辅助化疗的患者中,肿瘤退缩分级0、1、2、3级的患者分别为13、8、8、15例。其中,65.91%(29/44)的患者对治疗有反应。新辅助化疗后,化疗有效患者癌组织中ARHGAP8表达下调(<0.001)。ARHGAP蛋白水平低的患者反应率为92.86%,高于ARHGAP蛋白水平高的患者(53.33%)(=0.033)。结论 ARHGAP8在直肠癌组织中高表达。局部进展期低位直肠癌且ARHGAP8表达低的患者对XELOX方案新辅助化疗更敏感。ARHGAP8可作为直肠癌发生发展的潜在生物标志物及评估局部进展期低位直肠癌患者XELOX方案新辅助化疗疗效的重要指标。