A metabolic change is one of the tumour hallmarks, which has recently attracted a great amount of attention. One of the main metabolic characteristics of tumour cells is a high level of glycolysis even in the presence of oxygen, known as aerobic glycolysis or the Warburg effect. The energy production is much less in a glycolysis pathway than that in a tricarboxylic acid cycle. The Warburg effect constitutes a fundamental adaptation of tumour cells to a relatively hostile environment, and supports the evolution of aggressive and metastatic phenotypes. As a result, tumour glycolysis may become an attractive target for cancer therapy. Here, we research the effect of potential anticancer agents on tumour cells in vitro. In our study, we found a high sensitivity of tumour cells to anti-glycolityc drugs. In addition, tumour cells are more resistant to the agents studied in comparison with normal cells. We also observed an atypical cooperative interaction of tumour cells in the median lethal dose of drugs. They formed the specific morphological structure of the surviving cells. This behavior is not natural for the culture of tumour cells. Perhaps this is one of the mechanisms of cells’ adaptation to the aggressive environment.
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2 August 2016
PHYSICS OF CANCER: INTERDISCIPLINARY PROBLEMS AND CLINICAL APPLICATIONS (PC’16): Proceedings of the International Conference on Physics of Cancer: Interdisciplinary Problems and Clinical Applications 2016
22–25 March 2016
Tomsk, Russia
Research Article|
August 02 2016
Effect of anti-glycolytic agents on tumour cells in vitro
D. A. Korshunov;
D. A. Korshunov
a)
1
Tomsk Cancer Research Institute
, Kooperativny Street 5, Tomsk, 634050 Russia
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I. V. Kondakova
I. V. Kondakova
b)
1
Tomsk Cancer Research Institute
, Kooperativny Street 5, Tomsk, 634050 Russia
Search for other works by this author on:
a)
Corresponding author: [email protected]
AIP Conf. Proc. 1760, 020035 (2016)
Citation
D. A. Korshunov, I. V. Kondakova; Effect of anti-glycolytic agents on tumour cells in vitro. AIP Conf. Proc. 2 August 2016; 1760 (1): 020035. https://doi.org/10.1063/1.4960254
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