Circulating MicroRNA Profiles as Potential Biomarkers for Differentiated Thyroid Cancer Recurrence

被引:3
|
作者
Miljus, Jelena Jankovic [1 ,2 ]
Augusta Guillen-Sacoto, Maria [3 ]
Makiadi-Alvarado, Jennifer [2 ,4 ]
Wert-Lamas, Leon [2 ,5 ]
Ramirez-Moya, Julia [2 ,4 ]
Robledo, Mercedes [6 ,7 ]
Santisteban, Pilar [2 ,4 ]
Riesco-Eizaguirre, Garcilaso [3 ,4 ,8 ]
机构
[1] Univ Belgrade, Inst Applicat Nucl Energy INEP, Belgrade 11080, Serbia
[2] Univ Autonoma Madrid, Inst Invest Biomed Alberto Sols, Consejo Super Invest Cient, E-28029 Madrid, Spain
[3] Hosp Univ Mostoles, E-28935 Madrid, Spain
[4] Inst Salud Carlos III ISCIII, Ctr Invest Biomed Red Canc CIBERONC, Madrid 28029, Spain
[5] Harvard Med Sch, Dana Farber Canc Inst, Boston, MA 02215 USA
[6] Spanish Natl Canc Res Ctr CNIO, Hereditary Endocrine Canc Grp, Madrid 28029, Spain
[7] Ctr Invest Biomed Red Enfermedades Raras Ciberer, Madrid 28029, Spain
[8] Univ Francisco Vitoria, Mol Endocrinol Grp, E-28223 Madrid, Spain
来源
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM | 2022年 / 107卷 / 05期
关键词
microRNA; serum; thyroid cancer; recurrence; NGS; novel microRNA; PROGNOSTIC-SIGNIFICANCE; SERUM THYROGLOBULIN; PAPILLARY; DIAGNOSIS; EXPRESSION; NODULES; MICROCARCINOMA; CARCINOMA; MARKERS;
D O I
10.1210/clinem/dgac009
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Context Circulating microRNAs (miRNAs) are emerging biomarkers of thyroid cancer. Objective This study sought to identify the profile of circulating miRNAs and its response to human recombinant TSH (rhTSH) in thyroid cancer patients with recurrent/persistent disease. Methods We obtained serum samples from 30 patients with differentiated thyroid cancer, 14 with recurrent/persistent disease and 16 with complete remission. We used next-generation sequencing to define the miRnomes along with a comprehensive quantitative PCR (qPCR) validation using 2 different platforms. We made a transversal study by comparing serum miRNA profiles of patients with or without recurrent/persistent disease and a longitudinal study looking at differences before and after rhTSH stimulation. Selected miRNAs were then studied in human thyroid cancer cell lines TPC-1, FTC-133, and OCUT-2 in response to TSH stimulation. Results We could not demonstrate any consistent differences in serum profiles of known miRNAs between patients with and without recurrent/persistent disease or before and after rhTSH stimulation. However, our sequencing data revealed 2 putative novel miRNAs that rise with rhTSH stimulation in the serums of patients with recurrent/persistent disease. We further confirmed by qPCR the upregulation of these putative miRNAs both in serums and in TSH-stimulated cells. We also show miRNAs that are good candidates for housekeeping genes in the serum of patients independently of the levels of TSH. Conclusions The present study does not provide evidence that known miRNAs can be used as circulating markers for recurrence of thyroid cancer. However, we suggest that novel miRNA molecules may be related to thyroid cancer pathogenesis.
引用
收藏
页码:1280 / 1293
页数:14
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