Evaluation of the TRPM2 channel as a biomarker inbreast cancer using public databases analysis
Sumoza Toledo, Adriana y Espinoza Gabriel, Mario Iván y Montiel Condado, Dvorak (2016) Evaluation of the TRPM2 channel as a biomarker inbreast cancer using public databases analysis. Boletín médico del Hospital Infantil de México, 73 (6). pp. 397-404. ISSN 1665-1146
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Resumen
Background: Breast cancer is one of the most common malignancies affecting women. Recent investigations have revealed a major role of ion channels in cancer. The transient receptor potential melastatin-2 (TRPM2) is a plasma membrane and lysosomal channel with important roles in cell migration and cell death in immune cells and tumor cells. Methods: In this study, we investigated the prognostic value of TRPM2 channel in breast cancer, analyzing public databases compiled in OncomineTM (Thermo Fisher, Ann Arbor, MI) and online Kaplan-Meier Plotter platforms. Results: The results revealed that TRPM2 mRNA overexpression is significant in situ and invasive breast carcinoma compared to normal breast tissue. Furthermore, multi-gene validation using OncomineTM showed that this channel is coexpressed with proteins related to cellular migration, transformation, and apoptosis. On the other hand, Kaplan-Meier analysis exhibited that low expression of TRPM2 could be used to predict poor outcome in ER- and HER2+ breast carcinoma patients. Conclusions: TRPM2 is a promising biomarkerfor aggressiveness of breast cancer, and a potential target for the development of new therapies.
Tipo de elemento: | Article | ||||||||||||
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Palabras claves no controlados: | Breast cancer; TRPM2; Biomarker; Ion channel; Microarray | ||||||||||||
Materias: | R Medicina > RC Medicina Interna, Psiquiatría, Neurología | ||||||||||||
Divisiones: | Ciencias Biológicas | ||||||||||||
Usuario depositante: | Editor Repositorio | ||||||||||||
Creadores: |
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Fecha del depósito: | 08 Oct 2020 22:50 | ||||||||||||
Última modificación: | 08 Oct 2020 22:50 | ||||||||||||
URI: | http://eprints.uanl.mx/id/eprint/14501 |
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