miRNA-21 and miRNA-34a Are Potential Minimally Invasive Biomarkers for the Diagnosis of Pancreatic Ductal Adenocarcinoma

被引:71
作者
Alemar, Barbara [1 ,2 ]
Izetti, Patricia [1 ,2 ]
Gregorio, Cleandra [1 ,2 ]
Macedo, Gabriel S. [1 ,2 ]
Alves Castro, Mauro Antonio [3 ,4 ]
Osvaldt, Alessandro Bersch [5 ,6 ]
Matte, Ursula [1 ,7 ]
Ashton-Prolla, Patricia [1 ,2 ]
机构
[1] Univ Fed Rio Grande do Sul, Programa Postgrad Genet & Biol Mol, Porto Alegre, RS, Brazil
[2] Hosp Clin Porto Alegre, Ctr Pesquisa Expt, Lab Med Genom, Rua Ramiro Barcelos 2350, BR-90035903 Porto Alegre, RS, Brazil
[3] Hosp Clin Porto Alegre, Porto Alegre, RS, Brazil
[4] Univ Fed Parana, Lab Bioinformat & Biol Sistemas, Porto Alegre, RS, Brazil
[5] Hosp Clin Porto Alegre, Grp Vias Biliares & Pancreas Cirurgia Aparelho Di, Porto Alegre, RS, Brazil
[6] Programa Posgrad Med Ciencias Cirurg, Porto Alegre, RS, Brazil
[7] Hosp Clin Porto Alegre, Unidade Anal Mol & Prote, Ctr Pesquisa Expt, Porto Alegre, RS, Brazil
关键词
serum biomarkers; salivary biomarkers; microRNAs; miR-21; miR-34a; pancreatic ductal adenocarcinoma; MICRORNA EXPRESSION; CIRCULATING MICRORNAS; GENE-EXPRESSION; CANCER; SERUM; PCR; MARKER; BLOOD; OVEREXPRESSION; PROLIFERATION;
D O I
10.1097/MPA.0000000000000383
中图分类号
R57 [消化系及腹部疾病];
学科分类号
100201 [内科学];
摘要
Objectives Pancreatic ductal adenocarcinoma (PDAC) is one of the most deadly cancers, and its diagnosis often requires invasive procedures. Deregulated miRNA expression has been described in patients with PDAC. In this study, we analyzed the expression levels of 6 miRNAs (miR-21, -34a, -155, -196a, -200b, and -376a involved in PDAC tumorigenesis) in serum and salivary samples to assess their potential role as circulating diagnostics biomarkers. Methods Serum and salivary samples were collected from patients with PDAC and healthy controls, and miRNA levels were quantified using qRT-PCR. Twenty-four patients with PDAC and 10 healthy controls were recruited. Results A significant difference between PDAC and healthy groups was observed for the expression of miR-21 and miR-34a (P < 0.001 and P = 0.001) in serum samples. Both miRNAs accurately discriminated between the 2 groups, with an area under the curve for miR-21 and miR-34a of 0.889 (P = 0.001) and 0.865 (P = 0.002), respectively. In general, the expression of miRNAs between salivary samples did not differ. Conclusions Serum miR-21 and miR-34a are potentially useful diagnostic biomarkers of PDAC. In addition, our results suggest that these miRNAs are not differentially expressed in saliva, making them unsuitable for use as noninvasive biomarkers for diagnostic purposes.
引用
收藏
页码:84 / 92
页数:9
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