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Article

Activation of ARK5/miR-1181/HOXA10 axis promotes epithelial-mesenchymal transition in ovarian cancer

  • Authors:
    • Hai-Yan Zhang
    • Jian-Hua Li
    • Guang Li
    • Su-Rong Wang
  • View Affiliations / Copyright

    Affiliations: Gynaecology Ward-1, Linyi City People's Hospital, Shandong 276003, P.R. China, Lab, Linyi City People's Hospital, Shandong 276003, P.R. China, Gastrointestinal Surgery, Linyi City People's Hospital, Shandong 276003, P.R. China, Gynaecology Ward-3, Linyi City People's Hospital, Shandong 276003, P.R. China
  • Pages: 1193-1202
    |
    Published online on: July 7, 2015
       https://doi.org/10.3892/or.2015.4113
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Abstract

Epithelial ovarian cancer (EOC) is the sixth most common cancer in females worldwide and, although advances have been made in the detection, diagnosis and therapies for EOC, it remains the most lethal gynecologic malignancy in advanced countries. Nevertheless, relatively little is known concerning the molecular events that lead to the development of this highly aggressive disease. Elucidating the molecular mechanism involved in this disease may prove useful to understand the pathogenesis and progression of the disease, and to identify new targets for effective therapies. In the present study, we examined the role of ARK5 in ovarian cancer and normal matched tissues using western blot analysis and migration and invasion, and wound‑healing assays. The results showed that ARK5 was upregulated in ovarian cancer tissues, compared with adjacent normal tissues. Moreover, it promoted epithelial‑mesenchymal transition (EMT) and inhibited miR-1181 expression in ovarian cancer cells. Subsequent investigations showed that miR-1181 promoted mesenchymal-epithelial transition (MET) in ovarian cancer cells. Downstream target genes of miR-1181 were searched, and it was identified that miR-1181 degraded HOXA10 by targeting its 3' untranslated region (3'UTR) in ovarian cancer cells. The results confirmed that HOXA10 promoted EMT in ovarian cancer cells. Thus, activation of the ARK5/miR-1181/HOXA10 axis may be positively associated with EMT in ovarian cancer.
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Copy and paste a formatted citation
Spandidos Publications style
Zhang H, Li J, Li G and Wang S: Activation of ARK5/miR-1181/HOXA10 axis promotes epithelial-mesenchymal transition in ovarian cancer. Oncol Rep 34: 1193-1202, 2015.
APA
Zhang, H., Li, J., Li, G., & Wang, S. (2015). Activation of ARK5/miR-1181/HOXA10 axis promotes epithelial-mesenchymal transition in ovarian cancer. Oncology Reports, 34, 1193-1202. https://doi.org/10.3892/or.2015.4113
MLA
Zhang, H., Li, J., Li, G., Wang, S."Activation of ARK5/miR-1181/HOXA10 axis promotes epithelial-mesenchymal transition in ovarian cancer". Oncology Reports 34.3 (2015): 1193-1202.
Chicago
Zhang, H., Li, J., Li, G., Wang, S."Activation of ARK5/miR-1181/HOXA10 axis promotes epithelial-mesenchymal transition in ovarian cancer". Oncology Reports 34, no. 3 (2015): 1193-1202. https://doi.org/10.3892/or.2015.4113
Copy and paste a formatted citation
x
Spandidos Publications style
Zhang H, Li J, Li G and Wang S: Activation of ARK5/miR-1181/HOXA10 axis promotes epithelial-mesenchymal transition in ovarian cancer. Oncol Rep 34: 1193-1202, 2015.
APA
Zhang, H., Li, J., Li, G., & Wang, S. (2015). Activation of ARK5/miR-1181/HOXA10 axis promotes epithelial-mesenchymal transition in ovarian cancer. Oncology Reports, 34, 1193-1202. https://doi.org/10.3892/or.2015.4113
MLA
Zhang, H., Li, J., Li, G., Wang, S."Activation of ARK5/miR-1181/HOXA10 axis promotes epithelial-mesenchymal transition in ovarian cancer". Oncology Reports 34.3 (2015): 1193-1202.
Chicago
Zhang, H., Li, J., Li, G., Wang, S."Activation of ARK5/miR-1181/HOXA10 axis promotes epithelial-mesenchymal transition in ovarian cancer". Oncology Reports 34, no. 3 (2015): 1193-1202. https://doi.org/10.3892/or.2015.4113
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