Role of Twist1 transcription factor in thyroid tumor progression

Bencivenga, Tammaro Claudio (2011) Role of Twist1 transcription factor in thyroid tumor progression. [Tesi di dottorato] (Inedito)

Full text disponibile come:

[img]
Preview
PDF - Richiede un editor Pdf del tipo GSview, Xpdf o Adobe Acrobat Reader
13Mb

Abstract

Thyroid carcinomas are the most common endocrine tumors in humans, with a globally increasing incidence. Differentiated tumors, such as papillary (PTC) and follicular (FTC) thyroid cancers, are often curable with surgical resection and radiotherapy, whereas undifferentiated (anaplastic) thyroid carcinoma (ATC) is invariably lethal, due to the high invasiveness and insensitivity to radioiodine or chemotherapeutic treatment. Little is known about the molecular events that lead from the highly curable differentiated tumors to the very aggressive ATC. Through, a cDNA microarray analysis on different thyroid tumors we have isolated Twist1 as a gene upregulated in ATC. Twist1 is a highly conserved basic helix-loop-helix transcription factor that plays an important role in the development and progression of human cancer. Twist1 has been associated with epithelial-tomesenchymal transition (EMT) a key step during embryonic morphogenesis and in the progression of primary tumors toward metastasis. In this dissertation, we have shown that approximately 50% of ATCs upregulate Twist1 with respect to normal thyroids as well as to poorly- and well-differentiated thyroid carcinomas. Knockdown of Twist1 by RNA interference in ATC cells reduced cell migration and invasion and increased sensitivity to apoptosis. The ectopic expression of Twist1 in thyroid cells induced resistance to apoptosis and increased cell migration and invasion. To understand the molecular mechanisms through which Twist1 exert is biological effects in thyroid cancer cells, we have performed a microarray analysis of thyroid cancer cells ectopically expressing Twist1 in comparison to vector control cells. We have identified a set of 20 genes involved in migration, invasion and apoptosis; expression levels of these genes changed upon Twist1 overexpression or knockdown. Silencing of 5 of the 20 target genes reduced viability of thyroid cancer cells overexpressing Twist1. Thus, our data suggest that Twist1 plays a key role in determining malignant features of the anaplastic phenotype and identifies a set of Twist1 target genes that could be used as molecular target for the therapy of ATC.

Tipologia di documento:Tesi di dottorato
Parole chiave:Thyroid carcinoma; Twist1; Apoptosis
Settori scientifico-disciplinari MIUR:Area 06 Scienze mediche > MED/04 PATOLOGIA GENERALE
Coordinatori della Scuola di dottorato:
Coordinatore del Corso di dottoratoe-mail (se nota)
Santoro, Massimomasantor@unina.it
Tutor della Scuola di dottorato:
Tutor del Corso di dottoratoe-mail (se nota)
Salvatore, Giulianagsalvato@unina.it
Stato del full text:Accessibile
Data:30 Novembre 2011
Numero di pagine:125
Istituzione:Università di Napoli Federico II
Dipartimento o Struttura:Biologia e patologia cellullare e molecolare "L. Califano"
Stato dell'Eprint:Inedito
Scuola di dottorato:Medicina molecolare
Denominazione del dottorato:Oncologia ed endocrinologia molecolare
Ciclo di dottorato:24
Numero di sistema:8747
Depositato il:09 Dicembre 2011 11:18
Ultima modifica:25 Giugno 2012 09:52

Solo per gli Amministratori dell'archivio: edita il record