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DOI 10.1097/igc.0000000000000863

Медицинская библиотека · International journal of gynecological cancer : official journal of the International Gynecological Cancer Society · 2017

A New MicroRNA Expression Signature for Cervical Cancer.

Sun Ping, Shen Yong, Gong Jiao-Mei, Zhou Li-Li, Sheng Jia-He, Duan Fu-Jiao

СтатьяПоддержка исследования: вне правительства СШАПеревод в очереди

Аннотация

BACKGROUND

Cervical cancer is the second most common cancer among women worldwide. The potential of microRNAs as novel biomarkers in cervical cancer is growing.

OBJECTIVES

In this study, we investigated the functions and targets of miR-466 in cervical cancer tissues.

METHODS

Fresh cervical tissues were obtained from 157 patients with cervical cancer, cervical intraepithelial neoplasia (CIN), and healthy controls, and the tissues were immediately frozen in liquid nitrogen until use. The RNA was extracted and quantitative real-time polymerase chain reaction (PCR) was performed.

RESULTS

A total of 157 participants were summarized, including 56 patients with cervical cancer, 60 patients with CIN, and 49 healthy controls. The expression levels of miR-466 in cervical cancers (0.68) were higher than that in healthy controls (0.082) (P < 0.01). The average fold changes of miR-466 in the patients with CIN group and people group were 0.28 and 0.082, respectively (P < 0.01). It was a statistically significant difference in patients with lymph node involvement (P = 0.022). However, the expression of miR-466 was not correlated with International Federation of Gynecology and Obstetrics stages, tumor size, or vascular invasion (P = 0.506, P = 0.667, and P = 0.108, respectively).

CONCLUSIONS

Our results indicate that the aberrant expression of miR-466 is closely associated with the occurrence and development of cervical cancer.

Для цитирования: Sun Ping, Shen Yong, Gong Jiao-Mei, Zhou Li-Li, Sheng Jia-He, Duan Fu-Jiao. A New MicroRNA Expression Signature for Cervical Cancer.. International journal of gynecological cancer : official journal of the International Gynecological Cancer Society. 2017. DOI: 10.1097/igc.0000000000000863.

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