Vitamin D activates FBP1 to block the Warburg effect and modulate blast metabolism in acute myeloid leukemia.
Vitamin D activates FBP1 to block the Warburg effect and modulate blast metabolism in acute myeloid leukemia.
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DOI:
10.1186/s40364-022-00367-3
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发表时间:
2022-04-02
影响因子:
11.1
通讯作者:
Cao H
中科院分区:
文献类型:
--
作者:
Xu Y;Hino C;Baylink DJ;Xiao J;Reeves ME;Zhong JF;Mirshahidi S;Cao H
Acute myeloid leukemia (AML) has the lowest survival rate among the leukemias. Targeting intracellular metabolism and energy production in leukemic cells can be a promising therapeutic strategy for AML. Recently, we presented the successful use of vitamin D (1,25VD3) gene therapy to treat AML mouse models in vivo. In this study, recognizing the importance of 1,25VD3 as one of only 2 molecules (along with glucose) photosynthesized for energy during the beginning stage of life on this planet, we explored the functional role of 1,25VD3 in AML metabolism. Transcriptome database (RNA-seq) of four different AML cell lines revealed 17,757 genes responding to 1,25VD3-treatment. Moreover, we discovered that fructose-bisphosphatase 1 (FBP1) noticeably stands out as the only gene (out of 17,757 genes) with a 250-fold increase in gene expression, which is known to encode the key rate-limiting gluconeogenic enzyme fructose-1,6-bisphosphatase. The significant increased expression of FBP1 gene and proteins induced by 1,25VD3 was confirmed by qPCR, western blot, flow cytometry, immunocytochemistry and functional lactate assay. Additionally, 1,25VD3 was found to regulate different AML metabolic processes including gluconeogenesis, glycolysis, TCA, de novo nucleotide synthesis, etc. In summary, we provided the first evidence that 1,25 VD3-induced FBP1 overexpression might be a novel therapeutic target to block the “Warburg Effect” to reduce energy production in AML blasts. The online version contains supplementary material available at 10.1186/s40364-022-00367-3.
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DOI:
10.1016/j.jsbmb.2019.105399
发表时间:
2019-09-01
影响因子:
4.1
作者:
Maia-Ceciliano, Thais C.;Dutra, Rafaela R.;Mandarim-De-Lacerda, Carlos A.
通讯作者:
Mandarim-De-Lacerda, Carlos A.
影响因子:
11.4
作者:
Simonetti G;Mengucci C;Padella A;Fonzi E;Picone G;Delpino C;Nanni J;De Tommaso R;Franchini E;Papayannidis C;Marconi G;Pazzaglia M;Perricone M;Scarpi E;Fontana MC;Bruno S;Tebaldi M;Ferrari A;Bochicchio MT;Ghelli Luserna Di Rorà A;Ghetti M;Napolitano R;Astolfi A;Baldazzi C;Guadagnuolo V;Ottaviani E;Iacobucci I;Cavo M;Castellani G;Haferlach T;Remondini D;Capozzi F;Martinelli G
通讯作者:
Martinelli G
影响因子:
4.7
作者:
Marchwicka A;Cebrat M;Sampath P;Snieżewski L;Marcinkowska E
通讯作者:
Marcinkowska E
影响因子:
4.6
作者:
Corchete LA;Rojas EA;Alonso-López D;De Las Rivas J;Gutiérrez NC;Burguillo FJ
通讯作者:
Burguillo FJ
DOI:
10.1097/gim.0b013e31818b0d9b
发表时间:
2008-11
期刊:
Genetics in medicine : official journal of the American College of Medical Genetics
影响因子:
--
作者:
DeBerardinis RJ
通讯作者:
DeBerardinis RJ