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Mitochondrial recoupling: a novel therapeutic strategy for cancer?

British journal of cancer (2011-06-30)
G Baffy, Z Derdak, S C Robson
ABSTRACT

Recent findings link metabolic transformation of cancer cells to aberrant functions of mitochondrial uncoupling proteins (UCPs). By inducing proton leak, UCPs interfere with mitochondrial synthesis of adenosine 5'-triphosphate, which is also a key determinant of glycolytic pathways. In addition, UCP suppress the generation of superoxide, a byproduct of mitochondrial electron transport and a major source of oxidative stress. The near ubiquitous UCP2 becomes highly abundant in some cancers and may advance metabolic reprogramming, further disrupt tumour suppression, and promote chemoresistance. Here we review current evidence to suggest that inhibition of mitochondrial uncoupling may eliminate these responses and reveal novel anti-cancer strategies.

MATERIALS
Product Number
Brand
Product Description

Sigma-Aldrich
Adenosine 5′-triphosphate magnesium salt, ≥95%, bacterial
Sigma-Aldrich
Adenosine 5′-triphosphate dipotassium salt hydrate, from microbial, ≥92% (HPLC)
Sigma-Aldrich
Adenosine 5′-triphosphate (ATP) disodium salt hydrate, vial of 30 mg
Sigma-Aldrich
Adenosine 5′-triphosphate disodium salt hydrate, Grade II, ≥97% (HPLC), crystalline, from microbial
Sigma-Aldrich
Adenosine 5′-triphosphate di(tris) salt hydrate, ≥95%
Sigma-Aldrich
Adenosine 5′-triphosphate disodium salt hydrate, Grade I, ≥99%, from microbial
Sigma-Aldrich
Adenosine 5′-triphosphate disodium salt hydrate, BioXtra, ≥99% (HPLC), from microbial