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UCA1, a non‐protein‐coding RNA up‐regulated in bladder carcinoma and embryo, influencing cell growth and promoting invasion
Abstract
A non‐protein‐coding RNA,UCA1, has been cloned from human bladder TCC cell line BLZ‐211 by using 5′ and 3′ RACE. The UCA1 full‐length cDNA was 1442 bp. RT‐PCR analysis indicated that UCA1 is an embryonic development and bladder cancer‐associated RNA. The proliferative, migrative, invasive, and drug resistance behaviors of human bladder TCC cell line BLS‐211 were enhanced by exogenous UCA1 expression in vitro. Several potential target genes of UCA1 were identified through microarray analysis. Moreover, the expression of UCA1 also increased tumorigenic potential of BLS‐211 cells in nude mice. Results from the present study suggested that UCA1 might play a pivotal role in bladder cancer progression and embryonic development.
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Cited by
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Yang, G., Lu, X., & Yuan, L. (2014) · Biochimica et Biophysica Acta (BBA) - Gene Regulatory Mechanisms · doi:10.1016/j.bbagrm.2014.08.012 · Cited by 991
Kapusta, A., Kronenberg, Z., Lynch, V. J., Zhuo, X., Ramsay, L., Bourque, G., Yandell, M., & Feschotte, C. (2013) · PLoS Genetics · doi:10.1371/journal.pgen.1003470 · Cited by 687
Bian, Z., Jin, L., Zhang, J., Yin, Y., Quan, C., Hu, Y., Feng, Y., Liu, H., Fei, B., Mao, Y., et al. (2016) · Scientific Reports · doi:10.1038/srep23892 · Cited by 363
Xue, M., Chen, W., Xiang, A., Wang, R., Chen, H., Pan, J., Pang, H., An, H., Wang, X., Hou, H., et al. (2017) · Molecular Cancer · doi:10.1186/s12943-017-0714-8 · Cited by 359
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Metadata
- Authors
- Wang, F., Li, X., Xie, X., Zhao, L., & Chen, W.
- Venue
- FEBS Letters
- Publisher
- Wiley
- Published
- 2008-05-22
- Volume
- 582
- Issue
- 13
- Pages
- 1919-1927
- ISSN
- 0014-5793 (ISSN-L)
- 1873-3468
- OpenAlex
- W2049818912
- Cited by
- 339
- References
- 0
- FWCI
- 1.11
- Type
- journal article
- Language
- en
- Open access
- closed
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- Wang, F., Li, X., Xie, X., Zhao, L., & Chen, W. (2008). UCA1, a non‐protein‐coding RNA up‐regulated in bladder carcinoma and embryo, influencing cell growth and promoting invasion. FEBS Letters. https://doi.org/10.1016/j.febslet.2008.05.012
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