Abstract | OBJECTIVE: Recent studies have revealed that long noncoding RNAs (lncRNAs) play a crucial role in tumor progression. Ovarian cancer is a common type of fatal gynecological cancer worldwide. This study aims to investigate how lncRNADSCAM-AS1 functions in the progression of ovarian cancer. PATIENTS AND METHODS: DSCAM-AS1 expression of both ovarian cancer cells and 56 paired of tissue samples was detected by quantitative Real Time-Polymerase Chain Reaction (qRT-PCR). Moreover, the function of DSCAM-AS1 was identified via transwell assay, wound healing assay, colony formation assay and proliferation assay in vitro. The underlying mechanism was explored through qRT-PCR and Western blot assay. RESULTS: DSCAM-AS1 expression was remarkably upregulated in tumor tissues compared with that in the adjacent normal tissues. Besides, ovarian cancer proliferation, migration and invasion were promoted after overexpression of DSCAM-AS1 in vitro. Moreover, after overexpression of DSCAM-AS1, SOX4 was upregulated at mRNA and protein level in vitro. Furthermore, the expression of SOX4 in tumor tissues was positively correlated with the expression of DSCAM-AS1. CONCLUSIONS: The above results suggested that DSCAM-AS1 can promote cell migration, invasion and proliferation in ovarian cancer by upregulating SOX4, which may offer a new therapeutic intervention for patients with ovarian cancer.
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Authors | Y Li, J Hao, Y-M Jiang, Y Liu, S-H Zhang |
Journal | European review for medical and pharmacological sciences
(Eur Rev Med Pharmacol Sci)
Vol. 23
Issue 10
Pg. 4143-4148
(May 2019)
ISSN: 2284-0729 [Electronic] Italy |
PMID | 31173284
(Publication Type: Journal Article, Retracted Publication)
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Chemical References |
- RNA, Long Noncoding
- RNA, Messenger
- SOX4 protein, human
- SOXC Transcription Factors
- long noncoding RNA DSCAM-AS1, human
- Sincalide
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Topics |
- Cell Movement
- Cell Proliferation
- Disease Progression
- Female
- Humans
- Neoplasm Invasiveness
(genetics, pathology)
- Ovarian Neoplasms
(genetics, mortality)
- Prognosis
- RNA, Long Noncoding
(genetics)
- RNA, Messenger
(genetics)
- SOXC Transcription Factors
(metabolism)
- Sincalide
(metabolism)
- Up-Regulation
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