Go to:
Logótipo
Comuta visibilidade da coluna esquerda
Você está em: Start > Publications > View > Influence of the variable number of tandem repeats located in the promoter region of the thiopurine methyltransferase gene on enzymatic activity
Publication

Publications

Influence of the variable number of tandem repeats located in the promoter region of the thiopurine methyltransferase gene on enzymatic activity

Title
Influence of the variable number of tandem repeats located in the promoter region of the thiopurine methyltransferase gene on enzymatic activity
Type
Article in International Scientific Journal
Year
2001
Authors
Alves, S
(Author)
Other
The person does not belong to the institution. The person does not belong to the institution. The person does not belong to the institution. Without AUTHENTICUS Without ORCID
Amorim, A
(Author)
FCUP
View Personal Page You do not have permissions to view the institutional email. Search for Participant Publications View Authenticus page View ORCID page
Ferreira, F
(Author)
Other
The person does not belong to the institution. The person does not belong to the institution. The person does not belong to the institution. Without AUTHENTICUS Without ORCID
Prata, MJ
(Author)
FCUP
View Personal Page You do not have permissions to view the institutional email. Search for Participant Publications View Authenticus page View ORCID page
Journal
Vol. 70
Pages: 165-174
ISSN: 0009-9236
Publisher: Wiley-Blackwell
Scientific classification
FOS: Medical and Health sciences > Basic medicine
Other information
Authenticus ID: P-000-TP1
Abstract (EN): Background: The genetic polymorphism of thiopurine methyltransferase (TPMT) activity has a significant relevance in the clinical outcome of patients receiving thiopurine drugs as immunosupressive or anticancer therapies. Apart from several open reading frame mutations unequivocally associated with decreased TPMT activity, a variable number of tandem repeats (VNTR), located within the 5 ' untranslated region, was recently reported as also affecting gene expression. Aims and Methods: We have characterized both molecularly, by polymerase chain reaction-based techniques, and enzymatically, with an HPLC-based method, a sample of 143 Portuguese Caucasian individuals with the main objective of deepening the study of the TPMT genotype/phenotype relationship. Because two different repeated elements (A and B) do contribute to the overall VNTR variation, we set out to analyze their combined and individual effects on TPMT activity. Results: Allele VNTR*6 was found to be consistently associated with decreased levels of TPMT activity, supporting previous reports that the VNTR does affect levels of TPMT activity, although moderately and in a way not yet clearly defined. Furthermore, individual analysis of the A and B variations suggested that three B repeats was the likely motif influencing gene expression toward decreased transcription. Conclusions: Our hypothesis, which emphasizes the number of particular motifs within the VNTR internal structure more than the undiscriminated number of repeats as the potential causative factor affecting TPMT activity needs further support from future studies, namely, from enlarged population samples. However, the knowledge of the VNTR acting mechanism will represent an important step toward fully understanding how the phenotypic variability at the TPMT trait is modulated.
Language: English
Type (Professor's evaluation): Scientific
No. of pages: 10
Documents
We could not find any documents associated to the publication.
Related Publications

Of the same authors

The GSTM1 and GSTT1 genetic polymorphisms and susceptibility to acute lymphoblastic leukemia in children from north Portugal (2002)
Another Publication in an International Scientific Journal
Alves, S; Amorim, A; Ferreira, F; Norton, L; Prata, MJ
Tolerance to methotrexatetherapy in childhood acute lymphoblastic leukaemia: Importance of genetic polymorphisms in folate metabolic pathway (2007)
Other Publications
Oliveira, E; Quental, S; Ferreira, F; Alves, S; Gomes, V; Amorim, A; Prata, MJ
Thiopurine methyltransferase pharmacogenetics: alternative molecular diagnosis and preliminary data from Northern Portugal (1999)
Article in International Scientific Journal
Alves, S; Prata, MJ; Ferreira, F; Amorim, A
The MTHFR C677T and A1298C polymorphisms and susceptibility to childhood acute lymphoblastic leukemia in Portugal (2005)
Article in International Scientific Journal
Oliveira, E; Alves, S; Quental, S; Ferreira, F; Norton, L; Costa, T; Amorim, A; Prata, MJ
Screening of thiopurine S-methyltransferase mutations by horizontal conformation-sensitive gel electrophoresis (2000)
Article in International Scientific Journal
Alves, S; Prata, MJ; Ferreira, F; Amorim, A

See all (7)

Of the same journal

Clinical pharmacology information in summaries of product characteristics and package inserts (2007)
Article in International Scientific Journal
Arguello, B; Fernandez Llimos, F
Recommend this page Top
Copyright 1996-2025 © Faculdade de Direito da Universidade do Porto  I Terms and Conditions  I Acessibility  I Index A-Z
Page created on: 2025-07-20 at 16:56:57 | Privacy Policy | Personal Data Protection Policy | Whistleblowing