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Article

Microarray expression profiling of long non‑coding RNAs in epithelial ovarian cancer

  • Authors:
    • Ye Ding
    • Da‑Zheng Yang
    • Yong‑Ning Zhai
    • Kai Xue
    • Feng Xu
    • Xiao‑Yan Gu
    • Su‑Min Wang
  • View Affiliations / Copyright

    Affiliations: State Key Laboratory of Reproductive Medicine, Department of Endoscopic Diagnostic and Treatment Center, Obstetrics and Gynecology Hospital Affiliated to Nanjing Medical University, Nanjing, Jiangsu 210004, P.R. China
  • Pages: 2523-2530
    |
    Published online on: June 21, 2017
       https://doi.org/10.3892/ol.2017.6448
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Abstract

Although numerous long non-coding RNAs (lncRNAs) have been identified to be important in human cancer, their potential regulatory roles in epithelial tumorigenesis and tumor progression in ovarian cancer remain unclear. The purpose of the present study was to investigate lncRNAs that were differentially expressed (DE) in epithelial ovarian cancer and to explore their potential functions. The lncRNA profiles in five pairs of human epithelial ovarian cancer tissues and their adjacent normal tissues were described using microarrays. The results of the microarray analysis revealed that 672 upregulated and 549 downregulated (fold‑change ≥2.0) lncRNAs were DE between the cancerous and normal tissues. Reverse transcription‑quantitative polymerase chain reaction was used to validate the microarray results using four upregulated (RP11‑1C1.7, XLOC_003286, growth arrest‑specific 5 and ZNF295‑AS1) and four downregulated (protein tyrosine kinase 7, maternally expressed gene 3, AC079776.2 and ribosomal protein lateral stalk subunit P0 pseudogene 2) lncRNAs. Furthermore, gene ontology and pathway analyses were used to carry out functional analyses of the candidate genes of DE lncRNAs. The results identified lncRNAs with significantly altered expression profiles in human epithelial ovarian cancer cells compared with those in adjacent normal cells. These data offer new insights into the occurrence and development of epithelial ovarian cancer, and these lncRNAs may provide novel molecular biomarkers for further research on epithelial ovarian cancer.
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Copy and paste a formatted citation
Spandidos Publications style
Ding Y, Yang DZ, Zhai YN, Xue K, Xu F, Gu XY and Wang SM: Microarray expression profiling of long non‑coding RNAs in epithelial ovarian cancer. Oncol Lett 14: 2523-2530, 2017.
APA
Ding, Y., Yang, D., Zhai, Y., Xue, K., Xu, F., Gu, X., & Wang, S. (2017). Microarray expression profiling of long non‑coding RNAs in epithelial ovarian cancer. Oncology Letters, 14, 2523-2530. https://doi.org/10.3892/ol.2017.6448
MLA
Ding, Y., Yang, D., Zhai, Y., Xue, K., Xu, F., Gu, X., Wang, S."Microarray expression profiling of long non‑coding RNAs in epithelial ovarian cancer". Oncology Letters 14.2 (2017): 2523-2530.
Chicago
Ding, Y., Yang, D., Zhai, Y., Xue, K., Xu, F., Gu, X., Wang, S."Microarray expression profiling of long non‑coding RNAs in epithelial ovarian cancer". Oncology Letters 14, no. 2 (2017): 2523-2530. https://doi.org/10.3892/ol.2017.6448
Copy and paste a formatted citation
x
Spandidos Publications style
Ding Y, Yang DZ, Zhai YN, Xue K, Xu F, Gu XY and Wang SM: Microarray expression profiling of long non‑coding RNAs in epithelial ovarian cancer. Oncol Lett 14: 2523-2530, 2017.
APA
Ding, Y., Yang, D., Zhai, Y., Xue, K., Xu, F., Gu, X., & Wang, S. (2017). Microarray expression profiling of long non‑coding RNAs in epithelial ovarian cancer. Oncology Letters, 14, 2523-2530. https://doi.org/10.3892/ol.2017.6448
MLA
Ding, Y., Yang, D., Zhai, Y., Xue, K., Xu, F., Gu, X., Wang, S."Microarray expression profiling of long non‑coding RNAs in epithelial ovarian cancer". Oncology Letters 14.2 (2017): 2523-2530.
Chicago
Ding, Y., Yang, D., Zhai, Y., Xue, K., Xu, F., Gu, X., Wang, S."Microarray expression profiling of long non‑coding RNAs in epithelial ovarian cancer". Oncology Letters 14, no. 2 (2017): 2523-2530. https://doi.org/10.3892/ol.2017.6448
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