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KCNMA1 Expression Is Downregulated in Colorectal Cancer via Epigenetic Mechanisms
被引:22
|作者:
Basile, Maria Sofia
[1
]
Fagone, Paolo
[1
]
Mangano, Katia
[1
]
Mammana, Santa
[2
]
Magro, Gaetano
[3
]
Salvatorelli, Lucia
[3
]
Li Destri, Giovanni
[3
]
La Greca, Gaetano
[3
]
Nicoletti, Ferdinando
[1
]
Puleo, Stefano
[3
]
Pesce, Antonio
[3
]
机构:
[1] Univ Catania, Dept Biomed & Biotechnol Sci, Via S Sofia 89, I-95123 Catania, Italy
[2] IRCCS Ctr Neurolesi Bonino Pulejo, Str Statale 113, I-98124 Messina, Italy
[3] Univ Catania, Dept Med & Surg Sci & Adv Technol GF Ingrassia, Via Santa Sofia 86, I-95123 Catania, Italy
来源:
关键词:
KCNMA1;
Colorectal Cancer;
epigenetics;
DNA methylation;
mir-17-5p;
mir-31;
mir-211;
GENES;
D O I:
10.3390/cancers11020245
中图分类号:
R73 [肿瘤学];
学科分类号:
100214 ;
摘要:
KCNMA1 is a gene located at 10q22 that encodes the pore-forming alpha-subunit of the large-conductance Ca2+-activated K+ channel. KCNMA1 is down-regulated in gastric carcinoma tumors, through hypermethylation of its promoter. In the present study, we have evaluated the expression levels of KCNMA1 both in a mouse model of Colorectal Cancer (CRC) and in human CRC samples. Additionally, epigenetic mechanisms of KCNMA1 gene regulation were investigated. We observed a significant down-regulation of KCNMA1 both in a human and mouse model of CRC. No differences in KCNMA1 levels were, however, observed at different TNM stages. We also wanted to determine whether the modulation in KCNMA1 was dependent on epigenetic mechanisms. A statistically significant inverse correlation between KCNMA1 expression and mir-17-5p levels was observed in patients with CRC. Furthermore, in the tumor samples, we found a significant hypermethylation of the promoter, in the loci cg24113782 and cg25655799, compared to healthy tissue. Overall, our data suggest the possible use of KCNMA1 as a therapeutic target in the early stages of CRC.
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页数:13
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