Author:
Komarova Anastasia D,Sinyushkina Snezhana D,Shchechkin Ilia D,Druzhkova Irina N,Smirnova Sofia A,Terekhov Vitaliy M,Mozherov Artem M,Ignatova Nadezhda I,Nikonova Elena E,Shirshin Evgeny A,Shimolina Liubov E,Gamayunov Sergey V,Shcheslavskiy Vladislav I,Shirmanova Marina V
Abstract
AbstractHeterogeneity of tumor metabolism is an important, but still poorly understood aspect of tumor biology. Present work is focused on the visualization and quantification of cellular metabolic heterogeneity of colorectal cancer using fluorescence lifetime imaging (FLIM) of redox cofactor NAD(P)H. FLIM-microscopy of NAD(P)H was performed in vitro in four cancer cell lines, in vivo in the four types of tumors in mice and ex vivo in patients’ tumor samples. The dispersion and bimodality of the decay parameters were evaluated to quantify the intercellular metabolic heterogeneity. Our results demonstrate that patients’ tumors have significantly higher heterogeneity of energy metabolism compared with cultured cells and tumor xenografts, which was displayed as a wider and frequently bimodal distribution of a contribution of a free (glycolytic) fraction of NAD(P)H within a sample. Among patients’ tumors, the dispersion was larger in the high-grade and early stage ones, without, however, any association with bimodality. These results indicate that cell-level metabolic heterogeneity assessed from NAD(P)H FLIM has a potential to become a clinical prognostic factor.
Publisher
Cold Spring Harbor Laboratory