Enterobacteria impair host p53 tumor suppressor activity through mRNA destabilization.
Marie-Stéphanie AschtgenKonstantinos FragkoulisGema SanzStaffan NormarkGalina SelivanovaBirgitta Henriques-NormarkSylvain PeugetPublished in: Oncogene (2022)
Increasing evidence highlights the role of bacteria in the physiopathology of cancer. However, the underlying molecular mechanisms remains poorly understood. Several cancer-associated bacteria have been shown to produce toxins which interfere with the host defense against tumorigenesis. Here, we show that lipopolysaccharides from Klebsiella pneumoniae and other Enterobacteria strongly inhibit the host tumor suppressor p53 pathway through a novel mechanism of p53 regulation. We found that lipopolysaccharides destabilize TP53 mRNA through a TLR4-NF-κB-mediated inhibition of the RNA-binding factor Wig-1. Importantly, we show that K. pneumoniae disables two major tumor barriers, oncogene-induced DNA damage signaling and senescence, by impairing p53 transcriptional activity upon DNA damage and oncogenic stress. Furthermore, we found an inverse correlation between the levels of TLR4 and p53 mutation in colorectal tumors. Hence, our data suggest that the repression of p53 by Enterobacteria via TLR4 alleviates the selection pressure for p53 oncogenic mutations and shapes the genomic evolution of cancer.
Keyphrases
- dna damage
- klebsiella pneumoniae
- toll like receptor
- papillary thyroid
- inflammatory response
- oxidative stress
- immune response
- dna repair
- nuclear factor
- transcription factor
- squamous cell
- multidrug resistant
- diabetic rats
- gene expression
- binding protein
- lps induced
- endothelial cells
- stress induced
- high glucose
- electronic health record
- lymph node metastasis
- childhood cancer
- young adults
- mouse model
- heat stress
- heat shock