Literature DB >> 24025417

Diagnostic and prognostic value of plasma microRNA deregulation in nasopharyngeal carcinoma.

Xiong Liu1, Hua-Nan Luo1, Wen-Dong Tian1, Juan Lu1, Gang Li1, Lu Wang1, Bao Zhang2, Bi-Jun Liang1, Xiao-Hong Peng1, Shao-Xiong Lin1, Ying Peng3, Xiang-Ping Li1.   

Abstract

Nasopharyngeal carcinoma (NPC) is uncommon worldwide but often highly invasive in late stages. Due to its special location and lack of specific symptoms, NPC is hardly detected in regular medical examination at the beginning. Development of sensitive and specific biomarkers should help to save lives against this type of disease. In the present report, we investigated the value of plasma miRNAs for diagnosis and prognosis of NPC. Using candidate approach, we selected 21 miRNAs from literature to compare their expression levels in the plasma of NPC patients and controls. As a result, 5 miRNAs showed diagnostic potentials (P<0.01). Among them, miR-16, -21, -24, and -155 had increased levels in NPC patients, whereas the level of miR-378 was decreased. There was a negative correlation between plasma miRNA expression and cancer progression, where miR-21 was statistically significant in T and N staging and miR-16 and 24 were significant in N staging only. Combination of miR-16, -21, -24, -155, and -378 gives 87.7% of sensitivity and 82.0% of specificity for NPC diagnosis. Without miR-16, combination of the rest 4 miRNAs gives the same sensitivity but a slightly reduced specificity. After treatment, all 5 miRNAs were somewhat back to normal levels in patients without cancer recurrence but the prognostic value was not statistically significant. In conclusion, plasma miRNA expression is a useful biomarker for NPC diagnosis but not for its prognosis. More importantly, it is simple, effective, and non-invasive. Combination of several plasma miRNAs can increase both NPC diagnostic sensitivity and specificity.

Entities:  

Keywords:  NPC; biomarker; diagnosis; miRNA; nasopharyngeal carcinoma; plasma; prognosis

Mesh:

Substances:

Year:  2013        PMID: 24025417      PMCID: PMC3912036          DOI: 10.4161/cbt.26170

Source DB:  PubMed          Journal:  Cancer Biol Ther        ISSN: 1538-4047            Impact factor:   4.742


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