Please use this identifier to cite or link to this item: http://hdl.handle.net/1822/8707

TitleIncreasing expression of monocarboxylate transporters 1 and 4 along progression to invasive cervix carcinoma
Author(s)Pinheiro, Céline
Longatto Filho, Adhemar
Ferreira, Luísa
Pereira, Sónia Maria Miranda
Etlinger, Daniela
Moreira, M. A. R.
Jubé, L. F.
Queiroz, Geraldo Silva
Schmitt, Fernando C.
Baltazar, Fátima
KeywordsMonocarboxylate transporters
Cervical carcinoma
HPV
Issue dateOct-2008
PublisherLippincott, Williams & Wilkins
JournalInternational Journal of Gynecological Pathology
Citation"International Journal of Gynecological Pathology". ISSN 0277-1691. 27 : 4 (Oct. 2008) 568-574.
Abstract(s)Solid tumor cells are known to be highly glycolytic and, to prevent apoptosis by cellular acidosis, cells increase proton efflux through pH regulators, such as monocarboxylate transporters (MCTs). However, the role of these membrane proteins in solid tumor development and survival is not fully understood. We aimed to evaluate the expression of the MCTs isoforms 1, 2, and 4 in a large series of cervical lesions (neoplastic and non-neoplastic) and assess its clinical-pathologic significance. The series analyzed included 29 chronic cervicitis, 30 low-grade squamous intraepithelial lesions, 32 high-grade squamous intraepithelial lesions, 49 squamous cells carcinomas, 51 adenocarcinomas, and 30 adenosquamous carcinomas of the uterine cervix. Analysis of the expression of MCT isoforms 1, 2, and 4 was performed by immunohistochemistry with specific antibodies. Immunoreactions were evaluated both qualitatively and semiquantitatively. We found a significant increase in MCT expression from preinvasive to invasive squamous lesions and from normal glandular epithelium to adenocarcinomas. This is the first study evaluating the significance of MCT expression in lesions of the uterine cervix, including invasive carcinomas, and the results found herein led us to believe that these membrane proteins are involved in the progression to invasiveness in uterine cervix carcinoma.
TypeArticle
URIhttp://hdl.handle.net/1822/8707
DOI10.1097/PGP.0b013e31817b5b40
ISSN0277-1691
1538-7151
Publisher versionhttp://www.intjgynpathology.com
Peer-Reviewedyes
AccessRestricted access (UMinho)
Appears in Collections:ICVS - Artigos em Revistas Internacionais com Referee

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