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Chinese Journal of Clinicians(Electronic Edition) ›› 2022, Vol. 16 ›› Issue (01): 77-83. doi: 10.3877/cma.j.issn.1674-0785.2022.01.014

• Clinical Research • Previous Articles     Next Articles

Relationship of expression of lncRNA TPT1-AS1 and miR-30c-5p with pathological characteristics and prognosis in colon cancer

Zibing Fan1, Jing Shi1, Hongpeng Liu2, Yusong Shi2, Ying Qin2,()   

  1. 1. Department of General Surgery, the First Affiliated Hospital of Shenzhen University (Shenzhen Second People's Hospital), Shenzhen 518029, China
    2. Department of Gastrointestinal Surgery, the First Affiliated Hospital of Shenzhen University (Shenzhen Second People's Hospital), Shenzhen 518029, China
  • Received:2021-05-20 Online:2022-01-15 Published:2022-06-10
  • Contact: Ying Qin

Abstract:

Objective

To detect the expression of the long non-coding RNA (lncRNA) tumor protein translation regulator 1-antisense RNA1 (TPT1-AS1) and microRNA (miR)-30c-5p in colon cancer, and to analyze its relationship with pathological characteristics and prognosis.

Methods

A total of 117 patients with colon cancer who underwent radical or palliative surgery were selected from January 2015 to December 2017 at the First Affiliated Hospital of Shenzhen University. The colon cancer and adjacent tissues were surgically removed, and the expression levels of lncRNA TPT1-AS1 and miR-30c-5p in these tissues were detected by qRT-PCR. The relationship between the expression levels of lncRNA TPT1-AS1 and miR-30C-5p and the pathological features of colon cancer was analyzed, and the correlation between the expression levels of lncRNA TPT1-AS1 and miR-30C-5p in colon cancer tissues was analyzed by Pearson correlation test. Kaplan-Meier curve was used to calculate the 3-year cumulative survival rate of colon cancer patients with different lncRNA TPT1-AS1 and miR-30C-5P expression levels, and Cox regression analysis was performed to analyze the prognostic factors for colon cancer patients.

Results

The expression level of the lncRNA TPT1-AS1 was significantly higher (3.405±0.555 vs 1.766±0.096) and that of miR-30c-5p was significantly lower (0.306±0.146 vs 0.872±0.267) in colon cancer tissues than in adjacent tissues (P<0.05). The expression level of the lncRNA TPT1-AS1 was significantly higher in colon cancer TNM stage Ⅲ-Ⅳ than in stage Ⅰ-Ⅱ (3.651±0.579 vs 3.257±0.486), in T3-T4 colon cancer than in T1-T2 (3.523±0.601 vs 3.301±0.491), and in colon cancer with lymph node metastasis than in that without (3.614±0.585 vs 3.220±0.456) (P<0.05). The expression level of miR-30C-5P was significantly lower in colon cancer TNM stage Ⅲ-Ⅳ than that in stage Ⅰ-Ⅱ (0.251±0.126 vs 0.346±0.145), in T3-T4 colon cancer than in T1-T2 (0.270±0.119 vs 0.338±0.162), and in colon cancer with lymph node metastasis than in that without (0.255±0.125 vs 0.351±0.151) (P<0.05). Pearson correlation analysis showed that the expression of lncRNA1 TPT1-AS1 was negatively correlated with miR-30C-5P expression in colon cancer tissues (r=-0.572, P<0.05). Kaplan-Meier survival analysis showed that the 3-year cumulative survival rate (59.32% vs 87.93%) of the group with high lncRNA TPT1-AS1 expression was significantly lower than that of the group with low lncRNA1 TPT1-AS1 expression. The 3-year cumulative survival rate of the group with high miR-30C-5P expression (85.00% vs 61.40%) was significantly higher than that of the group with low miR-30C-5P expression (P<0.05). Multivariate Cox regression analysis showed that TNM stage Ⅲ-Ⅳ [hazard ratio (HR)=2.387, 95% confidence interval (CI): 1.004-5.671], lymph node metastasis (HR=2.667, 95%CI: 1.021-6.969), and TPT1-AS1≥3.405 (HR=2.023, 95%CI: 1.076-3.803) were independent prognostic risk factors for colon cancer patients, while mir-30C-5p ≥0.306 (HR=0.175, 95%CI: 0.012-0.423) was an independent protective factor (P<0.05).

Conclusion

The expression of lncRNA1 TPT1-AS1 in colon cancer tissue is significantly up-regulated, and the expression of miR-30c-5p is significantly down-regulated, both of which are associated with TNM stage, depth of invasion and lymph node metastasis, are independent prognostic factors for patients, and may become markers for prognostic evaluation of colon cancer.

Key words: Colon cancer, Long non-coding RNA, Tumor protein translation regulator 1, Antisense RNA1, MicroRNA-30c-5p

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