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A molecular hypothesis to explain direct and inverse co-morbidities between Alzheimer's Disease, Glioblastoma and Lung cancer

Sánchez-Valle, Jon ; Tejero, Héctor ; Ibáñez, Kristina ; Portero, José Luis ; Krallinger, Martin ; Al-Shahrour, Fátima ; Tabarés-Seisdedos, Rafael ; Baudot, Anaïs ; Valencia, Alfonso

Scientific reports, 2017-06, Vol.7 (1), p.4474-12, Article 4474 [Periódico revisado por pares]

England: Nature Publishing Group

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Título:
A molecular hypothesis to explain direct and inverse co-morbidities between Alzheimer's Disease, Glioblastoma and Lung cancer
Autor: Sánchez-Valle, Jon ; Tejero, Héctor ; Ibáñez, Kristina ; Portero, José Luis ; Krallinger, Martin ; Al-Shahrour, Fátima ; Tabarés-Seisdedos, Rafael ; Baudot, Anaïs ; Valencia, Alfonso
Assuntos: Alzheimer Disease ; Alzheimer's disease (AD) ; Alzheimer, Malaltia d ; Brain cancer ; Central Nervous System (CNS) ; Chemical Sciences ; Càncer ; Dinàmica molecular ; Disease ; Enginyeria biomèdica ; Fisiologia patològica ; Gliobastomas (GBM) ; Glioblastoma ; Health risk assessment ; Immune system ; Life Sciences ; Lung Cancer ; Lung diseases ; Mitochondria ; Molecular biology ; Morbidity ; Oxidative phosphorylation ; Phosphorylation ; Àrees temàtiques de la UPC
É parte de: Scientific reports, 2017-06, Vol.7 (1), p.4474-12, Article 4474
Notas: ObjectType-Article-1
SourceType-Scholarly Journals-1
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Descrição: Epidemiological studies indicate that patients suffering from Alzheimer's disease have a lower risk of developing lung cancer, and suggest a higher risk of developing glioblastoma. Here we explore the molecular scenarios that might underlie direct and inverse co-morbidities between these diseases. Transcriptomic meta-analyses reveal significant numbers of genes with inverse patterns of expression in Alzheimer's disease and lung cancer, and with similar patterns of expression in Alzheimer's disease and glioblastoma. These observations support the existence of molecular substrates that could at least partially account for these direct and inverse co-morbidity relationships. A functional analysis of the sets of deregulated genes points to the immune system, up-regulated in both Alzheimer's disease and glioblastoma, as a potential link between these two diseases. Mitochondrial metabolism is regulated oppositely in Alzheimer's disease and lung cancer, indicating that it may be involved in the inverse co-morbidity between these diseases. Finally, oxidative phosphorylation is a good candidate to play a dual role by decreasing or increasing the risk of lung cancer and glioblastoma in Alzheimer's disease.
Editor: England: Nature Publishing Group
Idioma: Inglês

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A molecular hypothesis to explain direct and inverse co-morbidities between Alzheimer's Disease, Glioblastoma and Lung cancer

Sánchez-Valle, Jon ; Tejero, Héctor ; Ibáñez, Kristina ; Portero, José Luis ; Krallinger, Martin ; Al-Shahrour, Fátima ; Tabarés-Seisdedos, Rafael ; Baudot, Anaïs ; Valencia, Alfonso

England: Nature Publishing Group

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