Expression of Selected miRNAs in Undifferentiated Carcinoma with Osteoclast-like Giant Cells (UCOGC) of the Pancreas: Comparison with Poorly Differentiated Pancreatic Ductal Adenocarcinoma

被引:1
作者
Popov, Alexey [1 ]
Hrudka, Jan [1 ]
Szabo, Arpad [1 ]
Oliverius, Martin [2 ]
Subrt, Zdenek [2 ]
Vranova, Jana [3 ]
Ciprova, Vanda [4 ]
Moravcova, Jana [1 ,5 ]
Mandys, Vaclav [1 ]
机构
[1] Charles Univ Prague, Univ Hosp Kralovske Vinohrady, Fac Med 3, Dept Pathol, Prague 10000, Czech Republic
[2] Charles Univ Prague, Univ Hosp Kralovske Vinohrady, Fac Med 3, Dept Surg, Prague 10000, Czech Republic
[3] Charles Univ Prague, Fac Med 3, Dept Med Biophys & Med Informat, Prague 10000, Czech Republic
[4] Charles Univ Prague, Gen Teaching Hosp, Fac Med 1, Inst Pathol, Prague 10000, Czech Republic
[5] Inst Clin & Expt Med, Clin & Transplant Pathol Ctr, Prague 14000, Czech Republic
关键词
pancreas; undifferentiated carcinoma with osteoclast-like giant cells; ductal adenocarcinoma; miRNA; MICRORNA EXPRESSION; TUMOR-SUPPRESSOR; CANCER; MIR-155; HYPOXIA; BIOMARKER; MIR-210; PATHWAY; INVASIVENESS; SIGNATURE;
D O I
10.3390/biomedicines12050962
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Undifferentiated carcinoma with osteoclast-like giant cells (UCOGC) of the pancreas represents a rare subtype of pancreatic ductal adenocarcinoma (PDAC). Despite a distinct morphology and specific clinical behavior, UCOGCs exhibit unexpected similarities in regard to DNA mutational profiles with conventional PDAC. Treating pancreatic ductal adenocarcinoma is particularly challenging, with limited prospects for cure. As with many other malignant neoplasms, the exploration of microRNAs (miRNAs, miRs) in regulating the biological characteristics of pancreatic cancer is undergoing extensive investigation to enhance tumor diagnostics and unveil the therapeutic possibilities. Herein, we evaluated the expression of miR-21, -96, -148a, -155, -196a, -210, and -217 in UCOGCs and poorly differentiated (grade 3, G3) PDACs. The expression of miR-21, miR-155, and miR-210 in both UCOGCs and G3 PDACs was significantly upregulated compared to the levels in normal tissue, while the levels of miR-148a and miR-217 were downregulated. We did not find any significant differences between cancerous and normal tissues for the expression of miR-96 and miR-196a in G3 PDACs, whereas miR-196a was slightly, but significantly, downregulated in UCOGCs. On the other hand, we have not observed significant differences in the expression of the majority of miRNAs between UCOGC and G3 PDAC, with the exception of miR-155. UCOGC samples demonstrated lower mean levels of miR-155 in comparison with those in G3 PDACs.
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页数:14
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