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Authors Ni W, Song E, Gong M, Li Y, Yao J, An R
Received 21 March 2017
Accepted for publication 6 May 2017
Published 19 June 2017 Volume 2017:10 Pages 3039—3047
DOI https://doi.org/10.2147/OTT.S137641
Checked for plagiarism Yes
Review by Single-blind
Peer reviewers approved by Dr Narasimha Reddy Parine
Peer reviewer comments 4
Editor who approved publication: Dr Samir Farghaly
Abstract: Renal cell carcinoma (RCC) is a common type of kidney cancer. Normally,
surgical treatment can prolong life, but only for patients with early stage
tumors. However, it is difficult for early detection strategies to distinguish
between benign and malignant kidney tumors. Therefore, potential biomarkers for
early diagnosis and prognosis of RCC are needed. Intriguingly, mounting
evidence has demonstrated that many long noncoding RNAs (lncRNAs) are strongly
linked to cancers. Indeed, promising RCC-associated lncRNA biomarkers have also
been identified. However, the functional and prognostic roles of the antisense
(AS) serum deprivation response (SDPR ) lncRNA
(SDPR-AS) in RCC remain largely unknown. The aims of this study were to investigate
the expression and prognostic relevance of SDPR-AS in RCC. We uncovered the
downregulated expressions of both lncRNA SDPR-AS and its protein-coding gene, SDPR , in RCC
tissues compared to the matched normal tissues. Furthermore, SDPR-AS and SDPR expressions were positively
correlated. Overexpression and knockdown experiments suggested that SDPR-AS and SDPR were coregulated in RCC cell lines. In
addition, overexpression of SDPR-AS suppressed cell migration and invasion, but
not cell growth. Furthermore, expression of SDPR-AS was associated with tumor
differentiation and lymphatic metastasis. Kaplan–Meier survival and log-rank
tests demonstrated the association of elevated expression of SDPR-AS with
increased overall survival. In conclusion, our results suggest that the SDPR-AS
may serve as a prognostic biomarker and therapeutic target of RCC.
Keywords: long
noncoding RNAs, metastasis, prognosis, renal cell carcinoma, suppressor
