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Energy sources identify metabolic phenotypes in pancreatic cancer
Author(s) -
Chen Liang,
Yi Qin,
Bo Zhang,
Shunrong Ji,
Si Shi,
Wenyan Xu,
Jiang Liu,
Jinfeng Xiang,
Dingkong Liang,
Qiangsheng Hu,
Liang Liu,
Chen Liu,
Guopei Luo,
Quanxing Ni,
Jin Xu,
Xianjun Yu
Publication year - 2016
Publication title -
acta biochimica et biophysica sinica
Language(s) - Uncategorized
Resource type - Journals
SCImago Journal Rank - 0.771
H-Index - 57
eISSN - 1745-7270
pISSN - 1672-9145
DOI - 10.1093/abbs/gmw097
Subject(s) - phenotype , biology , warburg effect , pancreatic cancer , phenotypic screening , metabolic pathway , glutaminolysis , cancer , cancer research , cancer cell , genetics , gene
Metabolic reprogramming is one of the emerging hallmarks of cancers. As a highly malignant tumor, pancreatic ductal adenocarcinoma (PDA) is not only a metabolic disease but also a heterogeneous disease. Heterogeneity induces PDA dependence on distinct nutritive substrates, thereby inducing different metabolic phenotypes. We stratified PDA into four phenotypes with distinct types of energy metabolism, including a Warburg phenotype, a reverse Warburg phenotype, a glutaminolysis phenotype, and a lipid-dependent phenotype. The four phenotypes possess distinct metabolic features and reprogram their metabolic pathways to adapt to stress. The metabolic type present in PDA should prompt differential imaging and serologic metabolite detection for diagnosis and prognosis. The targeting of an individual metabolic phenotype with corresponding metabolic inhibitors is considered a promising therapeutic approach and, in combination with chemotherapy, is expected to be a novel strategy for PDA treatment.

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