Popov Alexey, Hrudka Jan, Szabó Arpád, Oliverius Martin, Šubrt Zdeněk, Vránová Jana, Ciprová Vanda, Moravcová Jana, Mandys Václav
Department of Pathology, 3rd Faculty of Medicine, Charles University, University Hospital Královské Vinohrady, 100 00 Prague, Czech Republic.
Department of Surgery, 3rd Faculty of Medicine, Charles University, University Hospital Královské Vinohrady, 100 00 Prague, Czech Republic.
Biomedicines. 2024 Apr 26;12(5):962. doi: 10.3390/biomedicines12050962.
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.
胰腺未分化癌伴破骨细胞样巨细胞(UCOGC)是胰腺导管腺癌(PDAC)的一种罕见亚型。尽管其形态独特且临床行为特异,但UCOGC在DNA突变谱方面与传统PDAC表现出意想不到的相似性。治疗胰腺导管腺癌极具挑战性,治愈前景有限。与许多其他恶性肿瘤一样,对微小RNA(miRNA,miR)在调节胰腺癌生物学特性方面的探索正在广泛进行,以加强肿瘤诊断并揭示治疗可能性。在此,我们评估了miR-21、-96、-148a、-155、-196a、-210和-217在UCOGC和低分化(3级,G3)PDAC中的表达。与正常组织水平相比,UCOGC和G3 PDAC中miR-21、miR-155和miR-210的表达均显著上调,而miR-148a和miR-217的水平下调。在G3 PDAC中,我们未发现癌组织与正常组织在miR-96和miR-196a表达上有任何显著差异,而在UCOGC中miR-196a略有但显著下调。另一方面,除miR-155外,我们未观察到UCOGC与G3 PDAC在大多数miRNA表达上有显著差异。与G3 PDAC相比,UCOGC样本中miR-155的平均水平较低。