Interactions with stromal cells promote a more oxidized cancer cell redox state in pancreatic tumors.

Interactions with stromal cells promote a more oxidized cancer cell redox state in pancreatic tumors.
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DOI:
10.1126/sciadv.abg6383
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发表时间:
2022-01-21
期刊:
影响因子:
13.6
通讯作者:
Vander Heiden MG
Vander Heiden MG
中科院分区:
综合性期刊1区
文献类型:
--
作者:
Datta R;Sivanand S;Lau AN;Florek LV;Barbeau AM;Wyckoff J;Skala MC;Vander Heiden MG

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Access to electron acceptors supports oxidized biomass synthesis and can be limiting for cancer cell proliferation, but how cancer cells overcome this limitation in tumors is incompletely understood. Nontransformed cells in tumors can help cancer cells overcome metabolic limitations, particularly in pancreatic cancer, where pancreatic stellate cells (PSCs) promote cancer cell proliferation and tumor growth. However, whether PSCs affect the redox state of cancer cells is not known. By taking advantage of the endogenous fluorescence properties of reduced nicotinamide adenine dinucleotide and oxidized flavin adenine dinucleotide cofactors we use optical imaging to assess the redox state of pancreatic cancer cells and PSCs and find that direct interactions between PSCs and cancer cells promote a more oxidized state in cancer cells. This suggests that metabolic interaction between cancer cells and PSCs is a mechanism to overcome the redox limitations of cell proliferation in pancreatic cancer. Interactions between pancreatic stromal cells and pancreatic cancer cells affect the redox state of the cancer cells.
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