Department of Colorectal Surgery, the Second Hospital of Tianjin Medical University, Tianjin 300211, China.
Cell Mol Biol (Noisy-le-grand). 2022 May 22;68(1):192-200. doi: 10.14715/cmb/2022.68.1.23.
The current study aimed to explore the correlation between Mir-34A-3p, Mir-31, PLEK2 and the occurrence, development and prognosis of colorectal cancer. For this paper, 120 patients with colorectal cancer were selected as the study group, and their adjacent normal tissues were selected as the control group. The quantitative real-time PCR (QRT-PCR) method was used to detect miR-34a-3p and miR-31 in tissues, and the immunohistochemistry EnVision two-step method was used to detect PLEK2 positive expression. The expressions of miR -34a-3p, miR -31, and PLEK2 in colon cancer tissues and normal cancer tissues were compared, and the correlation between miR -34a-3p, miR -31, and PLEK2 and clinic-pathological characteristics of colorectal cancer patients were analyzed. The results showed that expression of miR -34a-3p, miR -31 and positive expression rate of PLEK2 in colorectal cancer tissues were higher than those in normal adjacent tissues (P<0.05). The expression of miR -34a-3p was related to tumor size, degree of tissue differentiation, lymph node metastasis and TNM stage (P < 0.05). The 3-year survival rate of miR -34a-3p with low expression was lower than miR -34a-3p with high expression, which was a protective factor affecting the poor prognosis of colorectal cancer (P < 0.05). The expression of miR -31 was related to tumor size and TNM stage. The 3-year survival rate of the group with high expression of miR -31 was lower than the group with low expression of miR -31, which was a risk factor affecting the poor prognosis of colorectal cancer (P < 0.05). PLEK2 positive expression was associated with lymph node metastasis, and the 3-year survival rate of the PLEK2 positive group was lower than the PLEK2 low expression group, which was a risk factor for poor prognosis of colorectal cancer (P < 0.05). In general, miR -34a-3p, miR -31, and PLEK2 are closely associated with the occurrence and development of colorectal cancer, and they are all influential factors affecting the prognosis of patients with colorectal cancer, which can provide a basis for the evaluation and treatment of patients, and are worthy of widespread clinical application.
本研究旨在探讨 Mir-34A-3p、Mir-31、PLEK2 与结直肠癌发生、发展和预后的相关性。为此,本文选取 120 例结直肠癌患者作为研究组,选取其相邻正常组织作为对照组。采用实时荧光定量 PCR(QRT-PCR)法检测组织中 miR-34a-3p 和 miR-31 的表达,采用免疫组化 EnVision 二步法检测 PLEK2 阳性表达。比较结直肠癌组织和正常癌组织中 miR-34a-3p、miR-31 和 PLEK2 的表达,并分析 miR-34a-3p、miR-31 和 PLEK2 与结直肠癌患者临床病理特征的关系。结果显示,结直肠癌组织中 miR-34a-3p、miR-31 和 PLEK2 的表达均高于正常相邻组织(P<0.05)。miR-34a-3p 的表达与肿瘤大小、组织分化程度、淋巴结转移及 TNM 分期有关(P<0.05)。miR-34a-3p 低表达患者的 3 年生存率低于 miR-34a-3p 高表达患者,是影响结直肠癌预后不良的保护因素(P<0.05)。miR-31 的表达与肿瘤大小及 TNM 分期有关。miR-31 高表达组的 3 年生存率低于 miR-31 低表达组,是影响结直肠癌预后不良的危险因素(P<0.05)。PLEK2 阳性表达与淋巴结转移有关,PLEK2 阳性组的 3 年生存率低于 PLEK2 低表达组,是影响结直肠癌预后不良的危险因素(P<0.05)。综上所述,miR-34a-3p、miR-31、PLEK2 与结直肠癌的发生发展密切相关,均是影响结直肠癌患者预后的影响因素,可为患者的评估和治疗提供依据,值得临床广泛应用。