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Table 2 List of exclusions from consideration as a reference miRNA based on the known, experimentally validated connections

From: A systemic approach to screening high-throughput RT-qPCR data for a suitable set of reference circulating miRNAs

microRNA

Reports on differential expression in serum or plasma due to specific clinical conditions

Reference

hsa-miR-222

Gastric cancer

[45]

hsa-miR-92a

Acute myeloid leukemia, acute myocardial infarction, potential marker of atherosclerosis, metabolic syndrome, bladder cancer, systemic lupus erythematosus

[46,47,48,49]

hsa-miR-27a

Acute pulmonary embolism, colorectal cancer

[52, 61]

hsa-miR-17

Elevated in many types of cancer, acute ischemic stroke, endometriosis, acute myocardial infarction

[62,63,64]

hsa-miR-24

Coronary heart disease, type 2 diabetes mellitus, early breast cancer

[65, 66]

hsa-miR-320a

Esophageal adenocarcinoma, Barret’s esophagus, arrhythmogenic cardiomyopathy

[67, 68]

hsa-miR-25

Osteosarcoma, breast cancer, papillary thyroid carcinoma, pancreatic cancer, gastric cancer, hepatocellular carcinoma, esophageal adenocarcinoma

[69,70,71,72,73,74]

hsa-miR-126

Non-small-cell lung cancer, chronic heart failure, acute myocardial infarction, ischemic stroke, type 2 diabetes mellitus

[64, 75,76,77,78]

hsa-miR-19b

Knee osteoarthritis, diabetic cardiomyopathy, acute myocardial infarction, gastric cancer, prostate cancer, lung cancer

[79,80,81,82,83,84]

hsa-miR-199a

Glioma, hepatocellular carcinoma, acute myocardial infarction, colorectal cancer, osteosarcoma

[85,86,87,88,89]

hsa-miR-30b

Active tuberculosis

[90]

hsa-miR-30c

HLTV-1 infection, Duchenne muscular dystrophy, active pulmonary tuberculosis

[91,92,93]

hsa-miR-374

Acute Graft-versus-Host disease

[94]

  1. We have performed a literature search in MEDLINE and PMC databases (through www.ncbi.mln.nih.gov/pubmed portal) looking for published evidence of pathological conditions influencing levels of circulating miRNAs included in the proposed reference set. Only human and experimentally validated studies were included, and the expression of a miRNA must have differed significantly between study and control groups