Metabolic reprogramming and redox adaptation in sorafenib-resistant leukemia cells: detected by untargeted metabolomics and stable isotope tracing analysis

Author:

You Xin12,Jiang Weiye1,Lu Wenhua1,Zhang Hui3,Yu Tiantian3,Tian Jingyu1,Wen Shijun1,Garcia-Manero Guillermo4,Huang Peng13,Hu Yumin13

Affiliation:

1. Department of Experimental Therapeutics; Sun Yat-sen University Cancer Center, State Key Laboratory of Oncology in South China, Collaborative Innovation Center for Cancer Medicine; 651 Dong Feng East Road Guangzhou 510060 Guangdong P. R. China

2. The First Department of Chemotherapy; The First Affiliated Hospital of Fujian Medical University; Fuzhou 350005 Fujian P. R. China

3. Metabolic Innovation Center, Zhongshan School of Medicine; Sun Yat-sen University; Guangzhou 510080 Guangdong P. R. China

4. Department of Leukemia; The University of Texas M.D. Anderson Cancer Center; Houston TX 77030 USA

Funder

Natural Science Foundation of Guangdong Province

Guangzhou Medicare Collaborative Innovation Program

Publisher

Wiley

Subject

Cancer Research,Oncology

Reference27 articles.

1. Treatment of FLT3-ITD positive acute myelogenous leukemia with allogeneic and autologous stem cell transplantation-results in 175 patients;Thiede;Blood.,2002

2. Phase I study of sorafenib in patients with refractory or relapsed acute leukemias;Borthakur;Haematologica,2011

3. Phase I study of quizartinib administered daily to patients with relapsed or refractory acute myeloid leukemia irrespective of FMS-like tyrosine kinase 3-internal tandem duplication status;Cortes;J Clin Oncol.,2013

4. Drug resistance in mutant FLT3-positive AML;Weisberg;Oncogene,2010

5. Secondary mutations as mediators of resistance to targeted therapy in leukemia;Daver;Blood,2015

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