Differential Expression of LncRNA in Bladder Cancer Development

被引:5
|
作者
Spirito, Lorenzo [1 ]
Maturi, Rufina [2 ]
Credendino, Sara Carmela [2 ]
Manfredi, Celeste [1 ]
Arcaniolo, Davide [1 ]
De Martino, Marco [3 ,4 ]
Esposito, Francesco [3 ]
Napolitano, Luigi [5 ]
Di Bello, Francesco [5 ]
Fusco, Alfredo [2 ,3 ]
Pallante, Pierlorenzo [3 ]
De Sio, Marco [1 ]
De Vita, Gabriella [2 ]
机构
[1] Univ Campania Luigi Vanvitelli, Dept Woman Child & Gen & Specialized Surg, Urol Unit, Via Crecchio 7, I-80138 Naples, Italy
[2] Univ Naples Federico II, Dept Mol Med & Med Biotechnol, Via Pansini 5, I-80131 Naples, Italy
[3] Natl Res Council CNR, Inst Expt Endocrinol & Oncol G Salvatore, Via Pansini 5, I-80131 Naples, Italy
[4] Univ Campania Luigi Vanvitelli, Dept Precis Med, Via Crecchio 7, I-80138 Naples, Italy
[5] Univ Naples Federico II, Dept Neurosci Reprod Sci & Odontostomatol, Urol Unit, Via Pansini 5, I-80131 Naples, Italy
关键词
bladder cancer; lncRNAs; gene expression; LONG NONCODING RNA; MIGRATION; PROLIFERATION; MORTALITY; EXPOSURE; RISK;
D O I
10.3390/diagnostics13101745
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Bladder cancer (BC) is the tenth most common cancer, with urothelial carcinoma representing about 90% of all BC, including neoplasms and carcinomas of different grades of malignancy. Urinary cytology has a significant role in BC screening and surveillance, although it has a low detection rate and high dependence on the pathologist's experience. The currently available biomarkers are not implemented into routine clinical practice due to high costs or low sensitivity. In recent years, the role of lncRNAs in BC has emerged, even though it is still poorly explored. We have previously shown that the lncRNAs Metallophosphoesterase Domain-Containing 2 Antisense RNA 1 (MPPED2-AS1), Rhabdomyosarcoma-2 Associated Transcript (RMST), Kelch-like protein 14 antisense (Klhl14AS) and Prader Willi/Angelman region RNA 5 (PAR5) are involved in the progression of different types of cancers. Here, we investigated the expression of these molecules in BC, first by interrogating the GEPIA database and observing a different distribution of expression levels between normal and cancer specimens. We then measured them in a cohort of neoplastic bladder lesions, either benign or malignant, from patients with suspicion of BC undergoing transurethral resection of bladder tumor (TURBT). The total RNA from biopsies was analyzed using qRT-PCR for the expression of the four lncRNA genes, showing differential expression of the investigated lncRNAs between normal tissue, benign lesions and cancers. In conclusion, the data reported here highlight the involvement of novel lncRNAs in BC development, whose altered expression could potentially affect the regulatory circuits in which these molecules are involved. Our study paves the way for testing lncRNA genes as markers for BC diagnosis and/or follow-up.
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页数:11
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