Journal of International Oncology ›› 2016, Vol. 43 ›› Issue (4): 267-270.doi: 10.3760/cma.j.issn.1673-422X.2016.04.007

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Expression and clinical significance of microRNA7 in serum of ovarian cancer patients

Jiao Limin, Liang Jin, Wang Qiong, Li Jiqiang   

  1. Department of Gynecology, Sixth People′s Hospital of Foshan Nanhai District of Guangdong Province, Foshan 528200, China
  • Online:2016-04-08 Published:2016-03-02
  • Contact: Li Jiqiang E-mail:banlangen12@126.com

Abstract: ObjectiveTo explore the expression and clinical significance of microRNA7 (miR7) in serum of ovarian cancer patients. MethodsSerum samples of 42 ovarian patients confirmed by pathological histology and 40 healthy women who underwent a physical exam were collected from January 2011 to January 2012 in the Sixth People′s Hospital of Foshan Nanhai District of Guangdong Province. Expression levels of miR7 in the serum samples of the two groups were examined using reverse transcriptionreal time polymerase chain reaction (RTPCR). The relationship between the expression of miR7 and the clinicopathologic feature of ovarian was analyzed. ResultsCompared with the controls, the expression of miR7 in the serum of ovarian cancer patients was significantly reduced (0.246±0.017 vs. 0.488±0.042), with a significant difference (t=11.23, P=0.01). The expression of miR7 in the serum of ovarian cancer patients was related to the clinical stage (t=10.12, P=0.01), pathological type (t=6.90, P=0.02), differentiation degree (t=4.46, P=0.03), regional lymph node or distant metastasis (t=5.62, P=0.02), but it was not related to the age (t=0.03, P=0.83). The patients with high miR7 expression had better overall survival than the patients with low miR7 expression (36.7 months vs. 24.3 months), with a significant difference (χ2=6.04, P=0.02). ConclusionThe expression of miR7 in serum of ovarian cancer patients is down regulated, which may be helpful for the overall assessment of ovarian carcinoma. miR7 may be one of the important prognostic indicators for ovarian carcinoma.

Key words: Ovarian neoplasms, MicroRNAs, Reverse transcriptase polymerase chain reaction