Combination of sulindac and dichloroacetate kills cancer cells via oxidative damage

Sulindac is an FDA-approved non-steroidal anti-inflammatory drug with documented anticancer activities. Our recent studies showed that sulindac selectively enhanced the killing of cancer cells exposed to oxidizing agents via production of reactive oxygen species (ROS) resulting in mitochondrial dysfunction. This effect of sulindac and oxidative stress on cancer cells could be related to the defect in respiration in cancer cells, first described by Warburg 50 years ago, known as the Warburg effect. We postulated that sulindac might enhance the selective killing of cancer cells when combined with any compound that alters mitochondrial respiration. To test this hypothesis we have used dichloroacetate (DCA), which is known to shift pyruvate metabolism away from lactic acid formation to respiration. One might expect that DCA, since it stimulates aerobic metabolism, could stress mitochondrial respiration in cancer cells, which would result in enhanced killing in the presence of sulindac. In this study, we have shown that the combination of sulindac and DCA enhances the selective killing of A549 and SCC25 cancer cells under the conditions used. As predicted, the mechanism of killing involves ROS production, mitochondrial dysfunction, JNK signaling and death by apoptosis. Our results suggest that the sulindac-DCA drug combination may provide an effective cancer therapy.

Medienart:

E-Artikel

Erscheinungsjahr:

2012

Erschienen:

2012

Enthalten in:

Zur Gesamtaufnahme - volume:7

Enthalten in:

PloS one - 7(2012), 7 vom: 01., Seite e39949

Sprache:

Englisch

Beteiligte Personen:

Ayyanathan, Kasirajan [VerfasserIn]
Kesaraju, Shailaja [VerfasserIn]
Dawson-Scully, Ken [VerfasserIn]
Weissbach, Herbert [VerfasserIn]

Links:

Volltext

Themen:

184SNS8VUH
9LSH52S3LQ
Dichloroacetic Acid
Journal Article
Reactive Oxygen Species
Research Support, N.I.H., Extramural
Research Support, Non-U.S. Gov't
Sulindac

Anmerkungen:

Date Completed 17.01.2013

Date Revised 21.10.2021

published: Print-Electronic

Citation Status MEDLINE

doi:

10.1371/journal.pone.0039949

funding:

Förderinstitution / Projekttitel:

PPN (Katalog-ID):

NLM219999007