Use this URL to cite or link to this record in EThOS: https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.731224
Title: Metabolic dysfunction and impairments in the DNA Damage Response : dissecting a pathomechanistic link between Microcephalic Primordial Dwarfisms and cancer cachexia
Author: Macpherson, Annie
ISNI:       0000 0004 6495 0160
Awarding Body: University of Sussex
Current Institution: University of Sussex
Date of Award: 2017
Availability of Full Text:
Access from EThOS:
Full text unavailable from EThOS. Please try the link below.
Access from Institution:
Abstract:
ATR (ataxia telangiectasia and Rad3-related) encodes master regulator of the DNA damage response ATR. Hypomorphic mutations in ATR result in microcephalic primordial dwarfism disorder Seckel Syndrome (SS). ATR-SS also presents with an apparent lack of subcutaneous fat. This potentially suggests ATR deficiency impairs lipogenic function. This is concerning considering the proposed use of small molecule kinase inhibitors of ATR (ATRis) as cancer chemotherapeutics. ATRi is a highly selective anti-cancer agent due to synthetic lethality in ATMor p53-deficient cells. An invariant feature of cancer is metabolic dysregulation, aggressive cancers can enforce systemic metabolic reprogramming resulting in drastic weight loss. Several screens have identified putative substrates for ATR in insulin signalling and metabolic pathways, indicating uncharacterised roles for ATR may exist here. Using several clinically relevant ATRis, I dissected the metabolic consequences of impaired ATR functionality on adipogenesis and lipogenic function of the 3T3-L1 cell line - widely utilised to investigate adipogenic differentiation. Acute ATRi treatment attenuated transcription of key adipogenic factors in differentiating preadipocytes, resulting in a failure to complete adipogenesis. I treated mature adipocytes chronically with ATRis, observing a striking transdifferentiation process known as browning - fat-storing white adipocytes underwent transcriptional reprogramming towards a thermogenic, brown adipocyte-like status. ATR deficiency generated this phenomenon by impinging on multiple pathways associated with metabolic regulation. I also observed striking cytoplasmic vacuolation and a disrupted autophagy response in every cell line treated with ATRis. I discovered ATR at the ER membrane, where ATRi-induced vacuolisation was derived from swollen endoplasmic reticulum (ER) concomitant with ER stress. I have characterised novel effects of ATR deficiency in adipocyte differentiation and metabolism, and ER and autophagic functionality. Autophagy and lipid metabolism are consistently deregulated in cancers, suggesting these results could lead to the generation of novel synthetic lethality approaches utilising ATRis and compounds targeting metabolic or autophagic pathways.
Supervisor: Not available Sponsor: Not available
Qualification Name: Thesis (Ph.D.) Qualification Level: Doctoral
EThOS ID: uk.bl.ethos.731224  DOI: Not available
Keywords: QH0447 Genes. Alleles. Genome
Share: