Circulating microRNAs as prognostic therapy biomarkers in head and neck cancer patients

被引:101
|
作者
Summerer, I. [1 ]
Unger, K. [1 ,2 ]
Braselmann, H. [1 ]
Schuettrumpf, L. [2 ,3 ]
Maihoefer, C. [2 ,3 ]
Baumeister, P. [2 ,4 ]
Kirchner, T. [5 ]
Niyazi, M. [2 ,3 ]
Sage, E. [6 ]
Specht, H. M. [6 ]
Multhoff, G. [6 ,7 ]
Moertl, S. [8 ]
Belka, C. [2 ,3 ]
Zitzelsberger, H. [1 ,2 ]
机构
[1] Helmholtz Ctr Munich, Res Unit Radiat Cytogenet, D-85764 Neuherberg, Germany
[2] Helmholtz Ctr Munich, Clin Cooperat Grp Personalized Radiotherapy Head, D-85764 Neuherberg, Germany
[3] Univ Munich, Dept Radiat Oncol, D-81377 Munich, Germany
[4] Univ Munich, Dept Otorhinolaryngol Head & Neck Surg, D-81377 Munich, Germany
[5] Univ Munich, Inst Pathol, D-80337 Munich, Germany
[6] Univ Munich, Dept Radiat Oncol, D-81675 Munich, Germany
[7] Helmholtz Ctr Munich, Clin Cooperat Grp Innate Immun, D-85764 Neuherberg, Germany
[8] Helmholtz Ctr Munich, Inst Radiat Biol, D-85764 Neuherberg, Germany
关键词
head and neck cancer; radiochemotherapy; circulating non-coding RNA; biomarker; prognosis; radiotherapy outcome; SQUAMOUS-CELL CARCINOMA; HUMAN-PAPILLOMAVIRUS; BREAST-CANCER; RADIATION-THERAPY; ESOPHAGEAL CANCER; PROSTATE-CANCER; MIRNAS; CHEMORADIOTHERAPY; MIR-142-3P; MARKERS;
D O I
10.1038/bjc.2015.111
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: The prediction of therapy response in head and neck squamous cell cancer (HNSCC) requires biomarkers, which are also a prerequisite for personalised therapy concepts. The current study aimed to identify therapy-responsive microRNAs (miRNAs) in the circulation that can serve as minimally invasive prognostic markers for HNSCC patients undergoing radiotherapy. Methods: We screened plasma miRNAs in a discovery cohort of HNSCC patients before therapy and after treatment. We further compared the plasma miRNAs of the patients to age-and sex-matched healthy controls. All miRNAs identified as biomarker candidates were then confirmed in an independent validation cohort of HNSCC patients and tested for correlation with the clinical outcome. Results: We identified a signature of eight plasma miRNAs that differentiated significantly (P = 0.003) between HNSCC patients and healthy donors. MiR-186-5p demonstrated the highest sensitivity and specificity to classify HNSCC patients and healthy individuals. All therapy-responsive and patient-specific miRNAs in plasma were also detectable in tumour tissues derived from the same patients. High expression of miR-142-3p, miR-186-5p, miR-195-5p, miR-374b-5p and miR-574-3p in the plasma correlated with worse prognosis. Conclusions: Circulating miR-142-3p, miR-186-5p, miR-195-5p, miR-374b-5p and miR-574-3p represent the most promising markers for prognosis and therapy monitoring in the plasma of HNSCC patients. We found strong evidence that the circulating therapy-responsive miRNAs are tumour related and were able to validate them in an independent cohort of HNSCC patients.
引用
收藏
页码:76 / 82
页数:7
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