Genetic alterations in poorly differentiated and undifferentiated thyroid carcicomas

Bibliographic Details
Main Author: Soares, Paula
Publication Date: 2011
Other Authors: Lima, Jorge, Almeida, Ana, Castro, Patrícia, Vinagre, João, Celstino, Ricardo, Couto, Joana Pinto, Prazeres, Hugo, Eloy, Catarina, Maximo, Valdemar, Simões, M. Sobrinho
Format: Article
Language: eng
Source: Repositórios Científicos de Acesso Aberto de Portugal (RCAAP)
Download full: https://hdl.handle.net/1822/15574
Summary: Thyroid gland presents a wide spectrum of tumours derived from follicular cells that range from well differentiated, papillary and follicular carcinoma (PTC and FTC, respectively), usually carrying a good prognosis, to the clinically aggressive, poorly differentiated (PDTC) and undifferentiated thyroid carcinoma (UTC). It is usually accepted that PDTC and UTC occur either de novo or progress from a pre-existing well differentiated carcinoma through a multistep process of genetic and epigenetic changes that lead to clonal expansion and neoplastic development. Mutations and epigenetic alterations in PDTC and UTC are far from being totally clarified. Assuming that PDTC and UTC may derive from well differentiated thyroid carcinomas (WDTC), it is expected that some PDTC and UTC would harbour genetic alterations that are typical of PTC and FTC. This is the case for some molecular markers (BRAF and NRAS) that are present in WDTC, PDTC and UTC. Other genes, namely P53, are almost exclusively detected in less differentiated and undifferentiated thyroid tumours, supporting a diagnosis of PDTC or, much more often, UTC. Thyroid-specific rearrangements RET/PTC and PAX8/PPARγ, on the other hand, are rarely found in PDTC and UTC, suggesting that these genetic alterations do not predispose cells to dedifferentiation. In the present review we have summarized the molecular changes associated with the two most aggressive types of thyroid cancer.
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spelling Genetic alterations in poorly differentiated and undifferentiated thyroid carcicomasPoorly differentiated thyroid carcinomaUndifferentiated thyroid carcinomaBRAFBeta-cateninRASP53PI3KTelomeraseβ-cateninScience & TechnologyThyroid gland presents a wide spectrum of tumours derived from follicular cells that range from well differentiated, papillary and follicular carcinoma (PTC and FTC, respectively), usually carrying a good prognosis, to the clinically aggressive, poorly differentiated (PDTC) and undifferentiated thyroid carcinoma (UTC). It is usually accepted that PDTC and UTC occur either de novo or progress from a pre-existing well differentiated carcinoma through a multistep process of genetic and epigenetic changes that lead to clonal expansion and neoplastic development. Mutations and epigenetic alterations in PDTC and UTC are far from being totally clarified. Assuming that PDTC and UTC may derive from well differentiated thyroid carcinomas (WDTC), it is expected that some PDTC and UTC would harbour genetic alterations that are typical of PTC and FTC. This is the case for some molecular markers (BRAF and NRAS) that are present in WDTC, PDTC and UTC. Other genes, namely P53, are almost exclusively detected in less differentiated and undifferentiated thyroid tumours, supporting a diagnosis of PDTC or, much more often, UTC. Thyroid-specific rearrangements RET/PTC and PAX8/PPARγ, on the other hand, are rarely found in PDTC and UTC, suggesting that these genetic alterations do not predispose cells to dedifferentiation. In the present review we have summarized the molecular changes associated with the two most aggressive types of thyroid cancer.Portuguese Foundation for Science and Technology through the program Ciência 2007 (VM), Ciência 2008 (JL) and grants to JPC (SFRH/BD/40260/2007) and to PC (SFRH/BPD/26553/2006), and a project grant (PTDC/SAU-OBD/101242/2008). Fundação Calouste Gulbenkian for grant to RC and JVBentham Science PublishersUniversidade do MinhoSoares, PaulaLima, JorgeAlmeida, AnaCastro, PatríciaVinagre, JoãoCelstino, RicardoCouto, Joana PintoPrazeres, HugoEloy, CatarinaMaximo, ValdemarSimões, M. Sobrinho20112011-01-01T00:00:00Zinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfhttps://hdl.handle.net/1822/15574eng1389-202910.2174/138920211798120853info:eu-repo/semantics/openAccessreponame:Repositórios Científicos de Acesso Aberto de Portugal (RCAAP)instname:FCCN, serviços digitais da FCT – Fundação para a Ciência e a Tecnologiainstacron:RCAAP2024-05-11T05:06:57Zoai:repositorium.sdum.uminho.pt:1822/15574Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireinfo@rcaap.ptopendoar:https://opendoar.ac.uk/repository/71602025-05-28T15:08:09.987426Repositórios Científicos de Acesso Aberto de Portugal (RCAAP) - FCCN, serviços digitais da FCT – Fundação para a Ciência e a Tecnologiafalse
dc.title.none.fl_str_mv Genetic alterations in poorly differentiated and undifferentiated thyroid carcicomas
title Genetic alterations in poorly differentiated and undifferentiated thyroid carcicomas
spellingShingle Genetic alterations in poorly differentiated and undifferentiated thyroid carcicomas
Soares, Paula
Poorly differentiated thyroid carcinoma
Undifferentiated thyroid carcinoma
BRAF
Beta-catenin
RAS
P53
PI3K
Telomerase
β-catenin
Science & Technology
title_short Genetic alterations in poorly differentiated and undifferentiated thyroid carcicomas
title_full Genetic alterations in poorly differentiated and undifferentiated thyroid carcicomas
title_fullStr Genetic alterations in poorly differentiated and undifferentiated thyroid carcicomas
title_full_unstemmed Genetic alterations in poorly differentiated and undifferentiated thyroid carcicomas
title_sort Genetic alterations in poorly differentiated and undifferentiated thyroid carcicomas
author Soares, Paula
author_facet Soares, Paula
Lima, Jorge
Almeida, Ana
Castro, Patrícia
Vinagre, João
Celstino, Ricardo
Couto, Joana Pinto
Prazeres, Hugo
Eloy, Catarina
Maximo, Valdemar
Simões, M. Sobrinho
author_role author
author2 Lima, Jorge
Almeida, Ana
Castro, Patrícia
Vinagre, João
Celstino, Ricardo
Couto, Joana Pinto
Prazeres, Hugo
Eloy, Catarina
Maximo, Valdemar
Simões, M. Sobrinho
author2_role author
author
author
author
author
author
author
author
author
author
dc.contributor.none.fl_str_mv Universidade do Minho
dc.contributor.author.fl_str_mv Soares, Paula
Lima, Jorge
Almeida, Ana
Castro, Patrícia
Vinagre, João
Celstino, Ricardo
Couto, Joana Pinto
Prazeres, Hugo
Eloy, Catarina
Maximo, Valdemar
Simões, M. Sobrinho
dc.subject.por.fl_str_mv Poorly differentiated thyroid carcinoma
Undifferentiated thyroid carcinoma
BRAF
Beta-catenin
RAS
P53
PI3K
Telomerase
β-catenin
Science & Technology
topic Poorly differentiated thyroid carcinoma
Undifferentiated thyroid carcinoma
BRAF
Beta-catenin
RAS
P53
PI3K
Telomerase
β-catenin
Science & Technology
description Thyroid gland presents a wide spectrum of tumours derived from follicular cells that range from well differentiated, papillary and follicular carcinoma (PTC and FTC, respectively), usually carrying a good prognosis, to the clinically aggressive, poorly differentiated (PDTC) and undifferentiated thyroid carcinoma (UTC). It is usually accepted that PDTC and UTC occur either de novo or progress from a pre-existing well differentiated carcinoma through a multistep process of genetic and epigenetic changes that lead to clonal expansion and neoplastic development. Mutations and epigenetic alterations in PDTC and UTC are far from being totally clarified. Assuming that PDTC and UTC may derive from well differentiated thyroid carcinomas (WDTC), it is expected that some PDTC and UTC would harbour genetic alterations that are typical of PTC and FTC. This is the case for some molecular markers (BRAF and NRAS) that are present in WDTC, PDTC and UTC. Other genes, namely P53, are almost exclusively detected in less differentiated and undifferentiated thyroid tumours, supporting a diagnosis of PDTC or, much more often, UTC. Thyroid-specific rearrangements RET/PTC and PAX8/PPARγ, on the other hand, are rarely found in PDTC and UTC, suggesting that these genetic alterations do not predispose cells to dedifferentiation. In the present review we have summarized the molecular changes associated with the two most aggressive types of thyroid cancer.
publishDate 2011
dc.date.none.fl_str_mv 2011
2011-01-01T00:00:00Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
format article
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dc.identifier.uri.fl_str_mv https://hdl.handle.net/1822/15574
url https://hdl.handle.net/1822/15574
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv 1389-2029
10.2174/138920211798120853
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dc.publisher.none.fl_str_mv Bentham Science Publishers
publisher.none.fl_str_mv Bentham Science Publishers
dc.source.none.fl_str_mv reponame:Repositórios Científicos de Acesso Aberto de Portugal (RCAAP)
instname:FCCN, serviços digitais da FCT – Fundação para a Ciência e a Tecnologia
instacron:RCAAP
instname_str FCCN, serviços digitais da FCT – Fundação para a Ciência e a Tecnologia
instacron_str RCAAP
institution RCAAP
reponame_str Repositórios Científicos de Acesso Aberto de Portugal (RCAAP)
collection Repositórios Científicos de Acesso Aberto de Portugal (RCAAP)
repository.name.fl_str_mv Repositórios Científicos de Acesso Aberto de Portugal (RCAAP) - FCCN, serviços digitais da FCT – Fundação para a Ciência e a Tecnologia
repository.mail.fl_str_mv info@rcaap.pt
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