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Metabolism-dependent secondary effect of anti-MAPK cancer therapy on DNA repair [QuantSeq_Q_siCTU2]

ABSTRACT: Metabolism-dependent secondary effect of anti-MAPK cancer therapy on DNA repair [QuantSeq_Q_siCTU2]

PROVIDER: PRJNA975076 | ENA |

REPOSITORIES: ENA

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Dataset's files

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			Action	DRS
	SRR24685113_1.fastq.gz	Fastqsanger.gz
	SRR24685113_2.fastq.gz	Fastqsanger.gz
	SRR24685114_1.fastq.gz	Fastqsanger.gz
	SRR24685114_2.fastq.gz	Fastqsanger.gz
	SRR24685115_1.fastq.gz	Fastqsanger.gz

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Project description:The translation-dependent effect of amino acid bioavailability on the nature of proteins that cells express could have major consequences on their phenotype. We report that the intracellular concentration decrease of amino acids like aspartate and glutamate in a melanoma cell line exposed to anti-cancer MAPK inhibitors (MAPKi) triggers ribosomal peaks in mRNA regions enriched in codons corresponding to these amino acids and in the translation-dependent degradation of mRNAs encoding proteins enriched in these amino acids. Since aspartate- and glutamate-rich proteins are involved in cell proliferation and DNA repair, we propose that MAPKi surviving cells degrade aspartate and glutamate to generate energy which simultaneously decreases their needs through the downregulation of gene products involved in cell proliferation. Moreover, the expression level decrease of aspartate- and glutamate-rich proteins involved in DNA repair increases as a side effect the probability of DNA damages and consequently the emergence of mutated cells in response to MAPKi.

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