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http://hdl.handle.net/10553/43065
Título: | Distribution of TYMS, MTHFR, p53 and MDR1 gene polymorphisms in patients with breast cancer treated with neoadjuvant chemotherapy | Autores/as: | Henríquez-Hernández, Luis Alberto Murias-Rosales, Adolfo González-Hernández, Ana de León, Antonio Cabrera Díaz-Chico, Nicolás Fernández-Pérez, Leandro |
Palabras clave: | Acute Lymphoblastic-Leukemia Methylenetetrahydrofolate Reductase C677T Colorectal-Cancer Thymidylate Synthase Clinical-Practice, et al. |
Fecha de publicación: | 2010 | Editor/a: | 1877-7821 | Publicación seriada: | Cancer Epidemiology | Resumen: | Purpose To investigate the role of TSER (TYMS), C677T (MTHFR), Arg72Pro (p53) and C3435T (MDR1) gene polymorphisms in breast cancer patients treated with 5-fluorouracil and cyclophosphamide-based neoadjuvant chemotherapy. Results Observed allelic frequencies were: TSER, (2) 0.54 and (3) 0.46; MTHFR C677T, (C) 0.59 and (T) 0.41; p53 Arg72Pro, (Arg) 0.73 and (Pro) 0.27; MDR1 C3435T, (C) 0.52 and (T) 0.48. MTHFR allele T and p53 allele Pro were strongly associated with toxicity due to chemotherapy (odds ratio, 7.1 (95% confidence interval, 1.4-36.1; p = 0.018) and 7.0 (95% confidence interval, 1.2-40.5; p = 0.029), respectively). Conclusion We introduced new data related to the contribution of p53 codon 72 to toxicity due to 5-fluorouracil and cyclophosphamide-based neoadjuvant chemotherapy in patients with breast cancer. (C) 2010 Elsevier Ltd. All rights reserved. | URI: | http://hdl.handle.net/10553/43065 | ISSN: | 1877-7821 | DOI: | 10.1016/j.canep.2010.06.013 | Fuente: | Cancer Epidemiology[ISSN 1877-7821],v. 34, p. 634-638 |
Colección: | Artículos |
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