Metabolic intervention on lipid synthesis converging pathways abrogates prostate cancer growth.


Autoria(s): Fritz V.; Benfodda Z.; Henriquet C.; Hure S.; Cristol J.P.; Michel F.; Carbonneau M.A.; Casas F.; Fajas L.
Data(s)

2013

Resumo

One of the most conserved features of all cancers is a profound reprogramming of cellular metabolism, favoring biosynthetic processes and limiting catalytic processes. With the acquired knowledge of some of these important changes, we have designed a combination therapy in order to force cancer cells to use a particular metabolic pathway that ultimately results in the accumulation of toxic products. This innovative approach consists of blocking lipid synthesis, at the same time that we force the cell, through the inhibition of AMP-activated kinase, to accumulate toxic intermediates, such as malonyl-coenzyme A (malonyl-CoA) or nicotinamide adenine dinucleotide phosphate. This results in excess of oxidative stress and cancer cell death. Our new therapeutic strategy, based on the manipulation of metabolic pathways, will certainly set up the basis for new upcoming studies defining a new paradigm of cancer treatment.

Identificador

https://serval.unil.ch/?id=serval:BIB_6008DD9E3699

isbn:1476-5594 (Electronic)

pmid:23208508

doi:10.1038/onc.2012.523

isiid:000325937900011

http://my.unil.ch/serval/document/BIB_6008DD9E3699.pdf

http://nbn-resolving.org/urn/resolver.pl?urn=urn:nbn:ch:serval-BIB_6008DD9E36999

Idioma(s)

en

Direitos

info:eu-repo/semantics/openAccess

Fonte

Oncogene, vol. 32, no. 42, pp. 5101-5110

Tipo

info:eu-repo/semantics/article

article