TY - JOUR
T1 - Circulating miR-182 is a biomarker of colorectal adenocarcinoma progression
AU - Perilli, Lisa
AU - Vicentini, Caterina
AU - Agostini, Marco
AU - Pizzini, Silvia
AU - Pizzi, Marco
AU - D'Angelo, Edoardo
AU - Bortoluzzi, Stefania
AU - Mandruzzato, Susanna
AU - Mammano, Enzo
AU - Rugge, Massimo
AU - Nitti, Donato
AU - Scarpa, Aldo
AU - Fassan, Matteo
AU - Zanovello, Paola
PY - 2014
Y1 - 2014
N2 - MiR-182 expression was evaluated by qRT-PCR and in situ hybridization in 20 tubular adenomas, 50 colorectal carcinoma (CRC), and 40 CRC liver metastases. Control samples obtained from patients with irritable bowel syndrome, or tumor-matched normal colon mucosa were analyzed (n=50). MiR-182 expression increased progressively and significantly along with the colorectal carcinogenesis cascade, and in CRC liver metastases. The inverse relation between miR-182 and the expression of its target gene ENTPD5 was investigated by immunohistochemical analysis. We observed that normal colocytes featured a strong ENTPD5 cytoplasmic expression whereas a significantly and progressively lower expression was present along with dedifferentiation of the histologic phenotype. Plasma samples from 51 CRC patients and controls were tested for miR-182 expression. Plasma miR-182 concentrations were significantly higher in CRC patients than in healthy controls or patients with colon polyps at endoscopy. Moreover, miR-182 plasma levels were significantly reduced in post-operative samples after radical hepatic metastasectomy compared to preoperative samples. Our results strengthen the hypothesis of a central role of miR-182 dysregulation in colon mucosa transformation, demonstrate the concomitant progressive down-regulation of ENTPD5 levels during colon carcinogenesis, and indicate the potential of circulating miR-182 as blood based biomarker for screening and monitoring CRC during the follow-up.
AB - MiR-182 expression was evaluated by qRT-PCR and in situ hybridization in 20 tubular adenomas, 50 colorectal carcinoma (CRC), and 40 CRC liver metastases. Control samples obtained from patients with irritable bowel syndrome, or tumor-matched normal colon mucosa were analyzed (n=50). MiR-182 expression increased progressively and significantly along with the colorectal carcinogenesis cascade, and in CRC liver metastases. The inverse relation between miR-182 and the expression of its target gene ENTPD5 was investigated by immunohistochemical analysis. We observed that normal colocytes featured a strong ENTPD5 cytoplasmic expression whereas a significantly and progressively lower expression was present along with dedifferentiation of the histologic phenotype. Plasma samples from 51 CRC patients and controls were tested for miR-182 expression. Plasma miR-182 concentrations were significantly higher in CRC patients than in healthy controls or patients with colon polyps at endoscopy. Moreover, miR-182 plasma levels were significantly reduced in post-operative samples after radical hepatic metastasectomy compared to preoperative samples. Our results strengthen the hypothesis of a central role of miR-182 dysregulation in colon mucosa transformation, demonstrate the concomitant progressive down-regulation of ENTPD5 levels during colon carcinogenesis, and indicate the potential of circulating miR-182 as blood based biomarker for screening and monitoring CRC during the follow-up.
KW - Biomarkers
KW - Colon cancer
KW - miR-182
KW - Plasma
UR - http://www.scopus.com/inward/record.url?scp=84907064971&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=84907064971&partnerID=8YFLogxK
U2 - 10.18632/oncotarget.2245
DO - 10.18632/oncotarget.2245
M3 - Article
C2 - 25115394
AN - SCOPUS:84907064971
SN - 1949-2553
VL - 5
SP - 6611
EP - 6619
JO - Oncotarget
JF - Oncotarget
IS - 16
ER -