Abstract
Background
Recent studies revealed that long noncoding RNAs (lncRNAs) play critical regulatory roles in cancer biology. PlncRNA-1 is one of lncRNAs that is associated with cell apoptosis and proliferation of prostate cancer.
Aim
This study aimed to assess the potential role of PlncRNA-1 in the pathogenesis of esophageal squamous cell carcinoma (ESCC).
Materials and Methods
Quantitative real-time polymerase chain reaction (qRT-PCR) was used to detect the expression level of PlncRNA-1 in 73 pairs of ESCC and their matched normal tissues. The correlation of PlncRNA-1 with clinicopathological features and clinical stages was also analyzed. Cancer cell proliferation and apoptosis were assessed following knock-down of PlncRNA-1 by MTT, colony formation assay, and flow cytometry.
Results
The expression of PlncRNA-1 was significantly higher in human ESCC compared with the adjacent noncancerous tissues (69.8 %, p < 0.05), and the high level of PlncRNA-1 expression was significantly correlated with advanced clinical stage (p < 0.01) and lymph node metastasis (p < 0.05). Furthermore, knockdown of PlncRNA-1 reduced cell proliferation and increased the apoptosis in vitro.
Conclusions
PlncRNA-1 plays an important role in ESCC cell proliferation. Overexpression of PlncRNA-1 is correlated with advanced tumor stage and lymph node metastasis, and may serve as a potential prognostic marker and therapeutic target for ESCC.
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Acknowledgments
This work was supported by the Graduate Research and Innovation Projects of Jiangsu Province (Grant No. CXLX_0567), the Foundation of Nanjing City Committee of Science and Technology (Grant No. 201108027), the Innovation Team of Science and Education Health Project of Jiangsu Province in 2011 (Grant No. Jiangsu Science and Education Health Project 2011 no.15) and the National Natural Science Foundation of China (Grant No. H1617/81201881).
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Wang, CM., Wu, QQ., Li, SQ. et al. Upregulation of the Long Non-coding RNA PlncRNA-1 Promotes Esophageal Squamous Carcinoma Cell Proliferation and Correlates with Advanced Clinical Stage. Dig Dis Sci 59, 591–597 (2014). https://doi.org/10.1007/s10620-013-2956-7
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DOI: https://doi.org/10.1007/s10620-013-2956-7