Can metabolic plasticity be a cause for cancer? Warburg-Waddington legacy revisited

• Published in: Clinical epigenetics 2011-08, Vol.2 (2), p.113-122
• Main Authors: Bhat, Paike Jayadeva, Darunte, Lalit, Kareenhalli, Venkatesh, Dandekar, Jaswandi, Kumar, Abhay
• Format: Article
• Language: English
• Subjects: Review
• ISSN: 1868-7075; 1868-7083
• DOI: 10.1007/s13148-011-0030-x

Fermentation of glucose to lactate in the presence of sufficient oxygen, known as aerobic glycolysis or Warburg effect, is a universal phenotype of cancer cells. Understanding its origin and role in cellular immortalization and transformation has attracted considerable attention in the recent past. Intriguingly, while we now know that Warburg effect is essential for tumor growth and development, it is thought to arise because of genetic and/or epigenetic changes. In contrast to the above, we propose that Warburg effect can also arise due to normal biochemical fluctuations, independent of genetic and epigenetic changes. Cells that have acquired Warburg effect proliferate rapidly to give rise to a population of heterogeneous progenitors of cancer cells. Such cells also generate more lactate and alter the fitness landscape. This dynamic fitness landscape facilitates evolution of cancer cells from its progenitors, in a fashion analogous to Darwinian evolution. Thus, sporadic cancer can also occur first by the acquisition of Warburg effect, then followed by mutation and selection. The idea proposed here circumvents the inherent difficulties associated with the current understanding of tumorigenesis, and is also consistent with many experimental and epidemiological observations. We discuss this model in the context of epigenetics as originally enunciated by Waddington. The online version of this article (doi:10.1007/s13148-011-0030-x) contains supplementary material, which is available to authorized users.