Evidence map›Paper›PMID 35596051›Full record

ArticleMolecular biology reports2022

Evaluation of potential of miR-8073 and miR-642 as diagnostic markers in pancreatic cancer.

Mohadeseh Fathi, Hamid Asadzadeh Aghdaie, Soudeh Ghafouri-Fard, Roshanak Shams

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Article in Molecular biology reports, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

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2 citing papers in PubMed.

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4 authors.

Mohadeseh FathiDepartment of Medical Genetics, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
Hamid Asadzadeh AghdaieResearch Institute for Gastroenterology and Liver Diseases, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
Soudeh Ghafouri-FardDepartment of Medical Genetics, Shahid Beheshti University of Medical Sciences, Tehran, Iran. s.ghafourifard@sbmu.ac.ir.ORCID http://orcid.org/0000-0002-0223-499X
Roshanak ShamsResearch Institute for Gastroenterology and Liver Diseases, Shahid Beheshti University of Medical Sciences, Tehran, Iran. shams.rosha.86@gmail.com.

Funding

shahid beheshti university of medical sciences shahid beheshti university of medical sciences
6 · The paper itself

Abstract

backgroundPancreatic cancer is a cancer with an insidious course. Since disease is often diagnosed at advanced stages, clinical outcome is impaired. Thus identification of biomarkers for this malignancy has importance in enhancement of patients' survival. METHODS AND

resultsIn the current study, we assessed expression levels of miR-8073 and miR-642 in the circulation of 50 patients with pancreatic cancer and 50 controls. Plasma levels of miR-8073 and miR-642 were significantly higher in patients with pancreatic cancer compared with controls (P value < 0.0001 and P value = 0.0068, respectively). Plasma levels of miR-642 were inversely correlated with albumin levels (R=-0.28, P value = 0.049), WBC count (R=-0.35, P value = 0.01), as well as CRP level (R=-0.30, P value = 0.035). On the other hand, levels of this miRNA were positively correlated with lipase level (R = 0.29, P value = 0.042). Levels of miR-8073 were not correlated with any of the available parameters. Plasma levels of miR-8073 could separate patients with pancreatic cancer from controls with AUC, sensitivity and specificity values of 0.82, 0.77 and 0.78, respectively. miR-642 could differentiate these two groups with AUC, sensitivity and specificity values of 0.63, 0.58 and 0.78, respectively. Combination of these two parameters resulted in AUC, sensitivity and specificity values of 0.79, 0.77 and 0.78, respectively.

conclusionsTaken together, these two miRNAs are suggested as possible blood markers for pancreatic cancer.

Indexed as

MicroRNAsPancreatic NeoplasmsBiomarkers, TumorGene Expression ProfilingHumansBiomarkers, TumorMicroRNAsMIRN642 microRNA, humanBiomarkermiR-642miR-8073Pancreatic cancer

Identifiers

PMID35596051

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