Hypoxic Cancer Cells Protect Themselves Against Damage: Search for a Single-Cell Indicator of This Protective Response by Polina Schwartsburd in Novel Approaches in Cancer Study
Abstract
Tumor hypoxia is accompanied by resistance to
many damaging therapeutic effects. This effect is often attributed to the loss
of the ability of normal and benign tumor cells to adapt their metabolism to
hypoxia, whereas cancer cells, on the contrary, acquire the ability to survive
and avoid an immune response under hypoxic conditions. Moreover, cancer cells
use hypoxia to reprogram their metabolism and induce antioxidant protection, in
particular by increasing the production of antioxidant molecules [NAD(P)H and
glutathione], which protect hypoxic cancer cells from the damaging effects of
free radicals. However, hypoxic cancer cells may differ one from another by the
efficiency of protection against damage; an indicator is required to assess
this efficiency. The goal of our work is the search for such a single-cell
endogenous indicator. For this, we measured endogenous NAD(P)H fluorescence in
single hypoxic cancer cells during their UV-induced damage [NAD(P)H
photodegradation], as well as determined their ability to restore NAD(P)H
fluorescence intensity after the damage/(photo)degradation. Most hypoxic cancer
(but not normal) cells were experimentally found to be capable of partially
restoring the damage with different efficiencies. Some hypoxic cancer cells
possess increased resistance to UV-induced damage. Such cells retained the
ability to partially restore NAD(P)H intensity even after 5-6 cycles of
repeated damage. Our studies enable recommending the NAD(P)H regenerative
response observed in hypoxic tumor cells as a prognostic indicator to assess
their potential resistance to damage. This indicator can be useful in choosing
new antitumor capabilities of specifically destroying cancer cells with
increased resistance to damage.
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