Endogenous p53 Inhibitor TIRR Dissociates Systemic Metabolic Health from Oncogenic Activity - RNAseq data

It is unclear whether metabolic health corresponds to reduced oncogenesis or vice versa. We study Tudor-interacting repair regulator (TIRR), an inhibitor of p53 binding protein 1 (53BP1)-mediated p53 activation, and the physiological consequences of enhancing tumor suppressor activity. Deleting TIRR selectively activates p53, significantly protecting against cancer but leading to a systemic metabolic imbalance in mice. TIRR-deficient mice are overweight and insulin resistant, even under normal chow diet. Similarly, reduced TIRR expression in human adipose tissue correlates with higher BMI and insulin resistance. Despite the metabolic challenges, TIRR loss improves p53 heterozygous (p53HET) mouse survival and correlates with enhanced progression-free survival in patients with various p53HET carcinomas. Finally, TIRR’s oncoprotective and metabolic effects are dependent on p53 and lost upon p53 deletion in TIRR-deficient mice, with glucose homeostasis and orexigenesis being primarily regulated by TIRR expression in the adipose tissue and the CNS, respectively, as evidenced by tissue-specific models. In summary, TIRR deletion provides a paradigm of metabolic deregulation accompanied by reduced oncogenesis. Comparative gene expression profiling analysis of RNA-seq data from mouse (C57Bl6 background) for: (1) perigonadal adipose tissue and brown adipose tissue models of Nudt16l1 knock-out (whole organism and adipose-specific) and Tp53 (whole organism) knock-out and their combinations; (2) liver, hypothalamus and perigonadal adipose tissue (2nd cohort) models of Nudt16l1 knock-out (whole organism); (3) mouse embryonic fibroblasts models of Nudt16l1 knock-out (whole organism) and Tp53 (whole organism) knock-out and their combinations.