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Multidrug resistance associated genes MRP1, MRP2 and MRP3 in primary and anthracycline exposed breast cancer.
Faneyte, Ian F; Kristel, Petra M P; van de Vijver, Marc J.
Afiliação
  • Faneyte IF; Department of Experimental Therapy, Cancer Institute / Antoni van Leeuwenhoek Hospital, Amsterdam, The Netherlands. m.vd.vijver@nki.nl
Anticancer Res ; 24(5A): 2931-9, 2004.
Article em En | MEDLINE | ID: mdl-15517899
ABSTRACT

BACKGROUND:

Multidrug resistance associated proteins MRP1, MRP2 and MRP3 confer in vitro multidrug resistance. We investigated their role in breast cancer resistance to anthracycline-based chemotherapy. MATERIALS AND

METHODS:

Using real-time reverse transcriptase polymerase chain reaction (RT-PCR) and immunohistochemistry (IHC), the expression of MRP1 - 3 was quantified in nine breast cancer cell lines and 30 breast carcinoma samples.

RESULTS:

MRP1 - 3 mRNA was detectable in all breast cancer cell lines and tumor samples. No increase of expression was detected between untreated carcinoma and post-neoadjuvant anthracycline treatment tumor samples. IHC failed to detect the proteins. MRP1 - 3 expression was not associated with tumor response to treatment or with outcome.

CONCLUSION:

MRP1 - 3 are expressed in breast cancer cells, but are not detected with IHC. We have found no evidence linking these proteins to clinical drug resistance in a small but well-documented series of breast cancer samples.
Assuntos
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Base de dados: MEDLINE Assunto principal: Neoplasias da Mama / Protocolos de Quimioterapia Combinada Antineoplásica / Antraciclinas / Genes MDR / Proteínas Associadas à Resistência a Múltiplos Medicamentos Tipo de estudo: Risk_factors_studies Limite: Humans Idioma: En Revista: Anticancer Res Ano de publicação: 2004 Tipo de documento: Article País de afiliação: Holanda
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Base de dados: MEDLINE Assunto principal: Neoplasias da Mama / Protocolos de Quimioterapia Combinada Antineoplásica / Antraciclinas / Genes MDR / Proteínas Associadas à Resistência a Múltiplos Medicamentos Tipo de estudo: Risk_factors_studies Limite: Humans Idioma: En Revista: Anticancer Res Ano de publicação: 2004 Tipo de documento: Article País de afiliação: Holanda