[Expression of CDC25A in non-small cell lung cancer and its relationship with let-7 gene]

Nan Fang Yi Ke Da Xue Xue Bao. 2020 Nov 30;40(11):1622-1627. doi: 10.12122/j.issn.1673-4254.2020.11.13.
[Article in Chinese]

Abstract

Objective: To investigate the expression of CDC25A in non- small cell lung cancer (NSCLC) tissues and explore its correlation with the clinicpathological features of the patients and the expressions of let-7a1 and let-7c.

Methods: We collected surgical specimens of pathologically confirmed NSCLC tissues and paired adjacent lung tissues from 44 patients and tissues of benign lung lesions from 9 patients. The expressions of CDC25A protein and mRNA in the tissues were detected by immunohistochemistry and fluorescence quantitative RT-PCR, respectively; the expressions of let-7a1 and let-7c mRNA were detected using tail-adding fluorescence quantitative RT-PCR.

Results: The positivity rate of CDC25A protein expression was significantly higher in NSCLC tissues than in the adjacent tissues and benign pulmonary lesions (P < 0.05). CDC25A protein expression in NSCLC was not correlated with the patients' age, gender, pathological type, degree of tumor differentiation, or clinical stages (P > 0.05), and was significantly correlated with smoking and lymph node metastasis (P < 0.05). CDC25A mRNA expression was also significantly higher in NSCLC tissues than in the adjacent tissues and benign pulmonary lesions (F=6.33, P < 0.05), and was similar between the latter two tissues (P > 0.05). Pearson correlation analysis showed that CDC25A expression had a significant negative correlation with let-7c expression in both NSCLC tissues (r=-0.42) and adjacent lung tissues (r=-0.40) but was not correlated with let-7a1 expression.

Conclusions: The expression level of CDC25A is significantly increased in NSCLC with a negative correlation with Let-7c expression, which identifies CDC25A as a possible downstream target gene of Let-7c.

目的: 明确细胞周期蛋白25A(CDC25A)在NSCLC组织中的表达及与临床病理特征的关系,并探讨其与miRNA let-7a1、let-7c表达的相关性。

方法: 收集53例肺组织手术标本,其中包括NSCLC组织44例,收集其癌组织和癌旁正常组织(病理证实),和良性肺疾病组织9例。免疫组化Elivision法检测CDC25A蛋白的表达;用Trizol法提取总RNA,采用荧光定量RT-PCR检测CDC25A mRNA的表达,加尾法荧光定量RT-PCR检测let-7a1和let-7c mRNA的表达。

结果: CDC25A蛋白表达的阳性率在NSCLC组织明显高于癌旁正常组织和良性肺疾病组织(P < 0.05)。NSCLC组织中CDC25A蛋白的表达与年龄、性别、病理类型、肿瘤分化程度、临床分期无关(P > 0.05),与吸烟、淋巴结转移相关(P < 0.05)。CDC25A mRNA在NSCLC组织中的表达量明显高于癌旁正常组织和良性肺疾病组织(F=6.33,P < 0.05),在癌旁正常组织和良性肺疾病组织中表达无明显差异(P > 0.05)。Pearson相关分析显示CDC25A与let-7c在NSCLC组织和癌旁正常组织中表达均呈明显负相关(r癌组织=-0.42,r癌旁正常组织=-0.40),与let-7a1之间无明显相关。

结论: CDC25A在NSCLC组织表达水平明显增高,且与let-7c表达呈明显负相关,推测CDC25A可能是let-7c的下游靶基因。

Keywords: CDC25A; let-7; microRNA; non-small cell lung cancer.

MeSH terms

  • Carcinoma, Non-Small-Cell Lung* / genetics
  • Gene Expression Regulation, Neoplastic
  • Humans
  • Lung
  • Lung Neoplasms* / genetics
  • Lymphatic Metastasis
  • MicroRNAs
  • RNA, Messenger / genetics
  • cdc25 Phosphatases

Substances

  • MicroRNAs
  • RNA, Messenger
  • mirnlet7 microRNA, human
  • CDC25A protein, human
  • cdc25 Phosphatases

Grants and funding

安徽省教育厅自然科学研究资助重点项目(KJ2018A0997);安徽省教育厅自然科学研究资助项目(KJ2010B113)