» Articles » PMID: 25337221

High Expression of Long Non-coding RNA SPRY4-IT1 Predicts Poor Prognosis of Clear Cell Renal Cell Carcinoma

Overview
Specialty Pathology
Date 2014 Oct 23
PMID 25337221
Citations 57
Authors
Affiliations
Soon will be listed here.
Abstract

Introduction: Long non-coding RNAs (lncRNAs) play a key role in cellular processes, such as cell growth, apoptosis, and carcinogenesis. lncRNAs SPRY4-IT1 has recently been identified to be involved in tumorigenesis of several cancers such as non-small cell lung cancer and esophageal squamous cell carcinoma. However, the role of SPRY4-IT1 in clear cell renal cell carcinoma (ccRCC) remains unclear.

Methods: The expression of SPRY4-IT1 was examined in ccRCC patients and renal cancer cell lines by using quantitative real-time PCR (qRT-PCR). The relationship between SPRY4-IT1 level and clinicopathological parameters of ccRCC was analyzed with the Kaplan-Meier method and Cox proportional hazards model. Small interfering RNA (siRNA) was used to suppress SPRY4-IT1 expression in renal cancer cell line 786-O. In vitro assays were performed to further explore its role in renal cancer progressio.

Results: The relative level of SPRY4-IT1 was significantly higher in ccRCC tissues compared to the adjacent normal renal tissues. And higher expression of SPRY4-IT1 was found in renal cancer cell lines compared with the normal human proximal tubule epithelial cell line HK-2. The ccRCC patients with higher SPRY4-IT1 expression had an advanced clinical stage and poorer prognosis than those with lower SPRY4-IT1 expression. Multivariate analyses by Cox's proportional hazard model revealed that expression of SPRY4-IT1 was an independent prognostic factor in ccRCC. In vitro assays, our results indicated that knockdown of SPRY4-IT1 reduced renal cancer cell proliferation, migration, and invasion.

Conclusions: Our data suggested that lncRNA SPRY4-IT1 might be considered as a potential prognostic indicator and a potential target for therapeutic intervention in RC.

Citing Articles

Renal cancer: signaling pathways and advances in targeted therapies.

Jiang A, Li J, He Z, Liu Y, Qiao K, Fang Y MedComm (2020). 2024; 5(8):e676.

PMID: 39092291 PMC: 11292401. DOI: 10.1002/mco2.676.


The Expression Patterns and Implications of , , and in Esophageal Adenocarcinoma.

Syllaios A, Gazouli M, Vailas M, Mylonas K, Sakellariou S, Sougioultzis S Int J Mol Sci. 2024; 25(1).

PMID: 38203269 PMC: 10778904. DOI: 10.3390/ijms25010098.


New insights into fibrotic signaling in renal cell carcinoma.

Chen J, Yiu W, Tang P, Tang S Front Cell Dev Biol. 2023; 11:1056964.

PMID: 36910160 PMC: 9996540. DOI: 10.3389/fcell.2023.1056964.


Emerging RNA-Based Therapeutic and Diagnostic Options: Recent Advances and Future Challenges in Genitourinary Cancers.

Tortora F, La Civita E, Trivedi P, Febbraio F, Terracciano D, Cimmino A Int J Mol Sci. 2023; 24(5).

PMID: 36902032 PMC: 10003365. DOI: 10.3390/ijms24054601.


Regulatory function of DNA methylation mediated lncRNAs in gastric cancer.

Li N, Zeng A, Wang Q, Chen M, Zhu S, Song L Cancer Cell Int. 2022; 22(1):227.

PMID: 35810299 PMC: 9270757. DOI: 10.1186/s12935-022-02648-1.


References
1.
Huttenhofer A, Schattner P, Polacek N . Non-coding RNAs: hope or hype?. Trends Genet. 2005; 21(5):289-97. DOI: 10.1016/j.tig.2005.03.007. View

2.
Xie H, Wu Q, Zhu B, Chen F, Ji L, Li S . Long noncoding RNA SPRY4-IT1 is upregulated in esophageal squamous cell carcinoma and associated with poor prognosis. Tumour Biol. 2014; 35(8):7743-54. DOI: 10.1007/s13277-014-2013-y. View

3.
Taft R, Pang K, Mercer T, Dinger M, Mattick J . Non-coding RNAs: regulators of disease. J Pathol. 2009; 220(2):126-39. DOI: 10.1002/path.2638. View

4.
Ljungberg B, Cowan N, Hanbury D, Hora M, Kuczyk M, Merseburger A . EAU guidelines on renal cell carcinoma: the 2010 update. Eur Urol. 2010; 58(3):398-406. DOI: 10.1016/j.eururo.2010.06.032. View

5.
Gibb E, Brown C, Lam W . The functional role of long non-coding RNA in human carcinomas. Mol Cancer. 2011; 10:38. PMC: 3098824. DOI: 10.1186/1476-4598-10-38. View