PRACTICAL ONCOLOGY JOURNAL ›› 2014, Vol. 28 ›› Issue (4): 299-304.doi: 10.11904/j.issn.1002-3070.2014.04.003

• Original Paper • Previous Articles     Next Articles

MLN64 gene and its research advancement in the field of carcinogenesis and progression of breast cancer

CAI Wei, KANG Hua   

  1. 1Gynecology Affiliated Tumor Hospital, Xinjiang Medical University , Urumqi 830011, china
  • Online:2014-08-28 Published:2014-07-31

Abstract: Objective The purpose of this study is to study the expression of miR-221 in cervical cancer tissues and its relationship with HPV infection. Methods HR-HPV infection was detected by HC2, and 30 cases of HR-HPV negative and 5 cases of HR-HPV positive cervical cancer tissues were collected. Meanwhile, 30 cases of normal cervical tissues in patients with benign disease were collected as control group. The expression of miR-221 was detected by RT-PCR, preliminarily investigating the relationship between miR-221 expression and the occurrence of cervical cancer and HPV infection. Through transfection of miR-221 and anti-miR-221 into HPV16-positive cervical carcinoma cell line Caski and HPV16-negative cervical carcinoma cell line C33a, we observed the role of miR-221 on the migration and invasion of Caski cells and C33a cells. Results Compared with normal cervical tissues, the expression of miR-221 in cervical cancer was significantly increased, the difference was statistically significant (P<0.01); and the expression of miR-221 is closely correlative to patients with or without lymph node metastasis, pathological grade and clinical stage (P<0.01); the expression of miR-221 in HR-HPV positive cervical cancer tissues was higher than in HR-HPV negative cervical cancer tissues (P<0.01); transfection of miR-221 and anti-miR-221 could promote or downregulate C33a and Caski cells migration and invasion, and the changes between two groups had statistical significance (P<0.05). Conclusion The increased expression of miR-221 in cervical cancer tissues is closely related to the occurrence and development of cervical cancer and HPV infection.

Key words: Cervical carcinoma, miR-221, HPV infection

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