American Association for Cancer Research
Browse
00085472can142615-sup-137415_2_supp_2830534_n555gr.png (116.15 kB)

Supplementary Figure S7 from Upregulation of Cytosolic Phosphoenolpyruvate Carboxykinase Is a Critical Metabolic Event in Melanoma Cells That Repopulate Tumors

Download (116.15 kB)
figure
posted on 2023-03-30, 23:51 authored by Yong Li, Shunqun Luo, Ruihua Ma, Jing Liu, Pingwei Xu, Huafeng Zhang, Ke Tang, Jingwei Ma, Yi Zhang, Xiaoyu Liang, Yanling Sun, Tiantian Ji, Ning Wang, Bo Huang

Supplementary Figure S7. High methylation in promoter region of PCK1 gene. B16 TRCs and control cells were used for DNA isolation.

History

ARTICLE ABSTRACT

Although metabolic defects have been investigated extensively in differentiated tumor cells, much less attention has been directed to the metabolic properties of stem-like cells that repopulate tumors [tumor-repopulating cells (TRC)]. Here, we show that melanoma TRCs cultured in three-dimensional soft fibrin gels reprogram glucose metabolism by hijacking the cytosolic enzyme phosphoenolpyruvate carboxykinase (PCK1), a key player in gluconeogenesis. Surprisingly, upregulated PCK1 in TRCs did not mediate gluconeogenesis but promoted glucose side-branch metabolism, including in the serine and glycerol-3-phosphate pathways. Moreover, this retrograde glucose carbon flow strengthened rather than antagonized glycolysis and glucose consumption. Silencing PCK1 or inhibiting its enzymatic activity slowed the growth of TRCs in vitro and impeded tumorigenesis in vivo. Overall, our work unveiled metabolic features of TRCs in melanoma that have implications for targeting a unique aspect of this disease. Cancer Res; 75(7); 1191–6. ©2015 AACR.

Usage metrics

    Cancer Research

    Licence

    Exports

    RefWorks
    BibTeX
    Ref. manager
    Endnote
    DataCite
    NLM
    DC