Home > Journals > Minerva Endocrinologica > Past Issues > Articles online first > Minerva Endocrinologica 2017 Sep 07

CURRENT ISSUE
 

ARTICLE TOOLS

Publication history
Reprints
Cite this article as

MINERVA ENDOCRINOLOGICA

A Journal on Endocrine System Diseases


Indexed/Abstracted in: EMBASE, PubMed/MEDLINE, Science Citation Index Expanded (SciSearch), Scopus
Impact Factor 1,383


eTOC

 

Minerva Endocrinologica 2017 Sep 07

DOI: 10.23736/S0391-1977.17.02735-3

Copyright © 2017 EDIZIONI MINERVA MEDICA

language: English

Evaluation of somatic genomic imbalances in thyroid carcinomas of follicular origin by CGH-based approaches

Federica BALDAN 1, Catia MIO 2, Lorenzo ALLEGRI 2, Nadia PASSON 3, Saverio M. LEPORE 4, Diego RUSSO 4, Giuseppe DAMANTE 2, 3

1 Department of Internal Medicine and Medical Specialties, "Sapienza" University of Rome, Rome, Italy; 2 Department of Medical Area, University of Udine, Udine, Italy; 3 Institute of Medical Genetics, Universitary Hospital, Udine, Italy; 4 Department of Health Sciences, “Magna Graecia” University of Catanzaro, Catanzaro, Italy


PDF  


INTRODUCTION: Application of distinct technologies of cancer genome analysis has provided important information for the molecular characterization of several human neoplasia, including follicular cell-derived thyroid carcinoma. Among them, comparative genomic hybridization (CGH)-based procedures have been extensively applied to evaluate genomic imbalances present in these tumours, obtaining data leading to an increase in the understanding of their complexity and diversity.
EVIDENCE ACQUISITION: In this review, after a brief overview of the most commonly used CGH-based technichs, we will describe the major results deriving from the most influential studies in the literature which used this approach to investigate the genomic aberrations of thyroid cancer cells.
EVIDENCE SINTHESIS: In most studies a small number of patients have been analyzed. Deletions and duplications at different chromosomal regions were detected in all investigated cohorts. A higher number of genomic imbalances has been detected in anaplastic or poorly differentiated thyroid carcinomas compared to well differentiated ones. Limitations in the interpretation of the results, as well the potential impact in the clinical practice are discussed.
CONCLUSIONS: Though a quite heterogeneous picture arises from results so far available, CGH array, combined with other methodologies as well as an accurate clinical management, may offer novel opportunities for a better stratification of thyroid cancer patients.


KEY WORDS: CGH array - Somatic mutation - Thyroid carcinoma

top of page

Publication History

Article first published online: September 7, 2017
Manuscript accepted: September 6, 2017
Manuscript received: September 4, 2017

Cite this article as

Baldan F, Mio C, Allegri L, Passon N, Lepore SM, Russo D et al. Evaluation of somatic genomic imbalances in thyroid carcinomas of follicular origin by CGH-based approaches. Minerva Endocrinol 2017 Sep 07. DOI: 10.23736/S0391-1977.17.02735-3

Corresponding author e-mail

giuseppe.damante@uniud.it