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Response to angiotensin blockade with irbesartan in a patient with metastatic colorectal cancer

BACKGROUND: A patient suffering from metastatic colorectal cancer, treatment-related toxicity and resistance to standard chemotherapy and radiation was assessed as part of a personalized oncogenomics initiative to derive potential alternative therapeutic strategies. PATIENTS AND METHODS: Whole-genom...

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Detalles Bibliográficos
Autores principales: Jones, M. R., Schrader, K. A., Shen, Y., Pleasance, E., Ch'ng, C., Dar, N., Yip, S., Renouf, D. J., Schein, J. E., Mungall, A. J., Zhao, Y., Moore, R., Ma, Y., Sheffield, B. S., Ng, T., Jones, S. J. M., Marra, M. A., Laskin, J., Lim, H. J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4843189/
https://www.ncbi.nlm.nih.gov/pubmed/27022066
http://dx.doi.org/10.1093/annonc/mdw060
Descripción
Sumario:BACKGROUND: A patient suffering from metastatic colorectal cancer, treatment-related toxicity and resistance to standard chemotherapy and radiation was assessed as part of a personalized oncogenomics initiative to derive potential alternative therapeutic strategies. PATIENTS AND METHODS: Whole-genome and transcriptome sequencing was used to interrogate a metastatic tumor refractory to standard treatments of a patient with mismatch repair-deficient metastatic colorectal cancer. RESULTS: Integrative genomic analysis indicated overexpression of the AP-1 transcriptional complex suggesting experimental therapeutic rationales, including blockade of the renin–angiotensin system. This led to the repurposing of the angiotensin II receptor antagonist, irbesartan, as an anticancer therapy, resulting in the patient experiencing a dramatic and durable response. CONCLUSIONS: This case highlights the utility of comprehensive integrative genomic profiling and bioinformatics analysis to provide hypothetical rationales for personalized treatment options.