Transcriptional and Metabolic Investigation in 5′-Nucleotidase Deficient Cancer Cell Lines

被引:2
作者
Cadassou, Octavia [1 ]
Forey, Prescillia [1 ]
Machon, Christelle [1 ,2 ]
Petrotto, Edoardo [1 ,3 ]
Chettab, Kamel [1 ]
Tozzi, Maria Grazia [3 ]
Guitton, Jerome [1 ,2 ]
Dumontet, Charles [1 ,2 ]
Cros-Perrial, Emeline [1 ]
Jordheim, Lars Petter [1 ]
机构
[1] Univ Lyon, Univ Claude Bernard Lyon 1, Ctr Rech Cancerol Lyon, Ctr Leon Berard,INSERM 1052,CNRS 5286, F-69008 Lyon, France
[2] Hosp Civils Lyon, Ctr Hosp Lyon Sud, F-69495 Pierre Benite, France
[3] Univ Pisa, Unita Biochim, Dipartimento Biol, Via San Zeno 51, I-56127 Pisa, Italy
关键词
CD73; cN-II; metabolic pathways; transcriptional regulation; CN-II; CD73; INHIBITION; IDENTIFICATION; REVEALS; PROTEIN;
D O I
10.3390/cells10112918
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Enzymes of nucleoside and nucleotide metabolism regulate important cellular processes with potential impacts on nucleotide-unrelated parameters. We have used a set of CRISPR/Cas9-modified cell models expressing both, one, or none of the 5 '-nucleotidases cN-II and CD73, together with RNA sequencing and targeted metabolomics, to decipher new regulatory roles of these proteins. We observed important transcriptional modifications between models as well as upon exposure to adenosine. Metabolite content varied differently between cell models in response to adenosine exposure but was rather similar in control conditions. Our original cell models allowed us to identify a new unobvious link between proteins in the nucleotide metabolism and other cellular pathways. Further analyses of our models, including additional experiments, could help us to better understand some of the roles played by these enzymes.
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页数:13
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