PRACTICAL ONCOLOGY JOURNAL ›› 2018, Vol. 32 ›› Issue (6): 538-544.doi: 10.11904/j.issn.1002-3070.2018.06.011

• Clinical Research • Previous Articles     Next Articles

Expression of miR-320a and CYLD in gastric cancer and its relationship with clinicopathological characteristics and prognosis

TANG Shuli, HE Kuangbang, ZHANG Chunhui, CHENG Jianan, ZHANG Yanqiao   

  1. Harbin Medical University Cancer Hospital, Harbin 150081, China
  • Received:2018-07-18 Online:2018-12-28 Published:2018-12-27

Abstract: Objective The aim of this study was to investigate the expression of miR-320a and cephalospermoma syndrome protein(CYLD)in patients with gastric cancer and its relationship with clinicopathological characteristics and prognosis. Methods A total of 460 patients with gastric cancer underwent tumor resection in our hospital from March 2013 to November 2014 were enrolled.Tumor tissues, non-tumor gastric mucosa tissues and normal tissues were collected.The expression of miR-320a and CYLD at levels of mRNA and protein were detected by Real-Time PCR, immunohistochemistry and Western blotting.The relationship between the expression of miR-320a and CYLD, and the clinicopathological features & prognosis of gastric cancer patients was analyzed. Results The relative expression of miR-320a and CYLD at the mRNA level in tumor tissues was(0.37±0.09), (0.91±0.23), and the relative expression in non-tumor tissues was(0.86±0.15), (1.56±0.42), respectively.The relative expression of miR-320a and CYLD mRNA in tumor tissues was significantly different from non-tumor tissues(t=60.078, 29.113, P=0.000), the positive expression rate of CYLD protein in tumor tissues was 43.48% when compared to 73.91% in non-tumor tissues.The difference was statistically significant(χ2=86.624, P=0.003).The expression level of miR-320a was significantly associated with the diameter of the tumor and lymph node metastasis(χ2=25.859 and 13.742, P<0.05).The expression of CYLD was also significantly associated with the TNM stage and degree of tumor differentiation(χ2=37.725 and 59.323, P<0.05).The median survival of patients with low miR-320a expression(20.36 months, 95% CI:19.252~21.462 months)and those with high miR-320a expression(28.29 months, 95% CI:27.158~29.412 months)were statistically significant(χ2=87.967, P<0.001).The median survival of patients with CYLD negative expression(17.70 months, 95% CI:16.599~18.796 months)and those with CYLD positive expression(26.74 months, 95% CI:25.474~27.997 months)were statistically significant(χ2=109.887, P<0.001);The median survival of patients with the co-expressed miR-320a and CYLD was(29.01 months, 95% CI:26.831~28.946 months)and those with the non-co-expressed miR-320a and CYLD(17.13 months, 95% CI:17.214~19.568 months)were statistically significant(χ2=117.680, P<0.001).There showed a positive correlation between the expression of miR-320a and CYLD at mRNA level(r=0.607, P<0.001);miR-320a at the low expression, CYLD at the negative expression, TNM staging, lymph node metastasis and degree of tumor differentiation were independent risk factors for the prognosis of gastric cancer(HR=1.939, 2.180, 1.561, 1.719, 1.608, 95% CI:1.141~3.295, 1.252~3.796, 1.014~2.403, 1.115~2.650, 1.097~2.357, respectively)(P<0.05). Conclusion The expressions of miR-320a and CYLD in tumor tissues of patients with gastric cancer is significantly decreased, which is related to the occurrence and development of diseases, and poor prognosis.It is a potential target for diagnosis and treatment of gastric cancer.

Key words: MiR-320a, Cylindromatosis, Gastric cancer, Prognosis

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