FB2026_02 , released June 18, 2026
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Citation
Newton, H., Wang, Y.F., Camplese, L., Mokochinski, J.B., Kramer, H.B., Brown, A.E.X., Fets, L., Hirabayashi, S. (2020). Systemic muscle wasting and coordinated tumour response drive tumourigenesis.  Nat. Commun. 11(1): 4653.
FlyBase ID
FBrf0246777
Publication Type
Research paper
Abstract
Cancer cells demand excess nutrients to support their proliferation, but how tumours exploit extracellular amino acids during systemic metabolic perturbations remain incompletely understood. Here, we use a Drosophila model of high-sugar diet (HSD)-enhanced tumourigenesis to uncover a systemic host-tumour metabolic circuit that supports tumour growth. We demonstrate coordinate induction of systemic muscle wasting with tumour-autonomous Yorkie-mediated SLC36-family amino acid transporter expression as a proline-scavenging programme to drive tumourigenesis. We identify Indole-3-propionic acid as an optimal amino acid derivative to rationally target the proline-dependency of tumour growth. Insights from this whole-animal Drosophila model provide a powerful approach towards the identification and therapeutic exploitation of the amino acid vulnerabilities of tumourigenesis in the context of a perturbed systemic metabolic network.
PubMed ID
PubMed Central ID
PMC7495438 (PMC) (EuropePMC)
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Secondary IDs
    Language of Publication
    English
    Additional Languages of Abstract
    Parent Publication
    Publication Type
    Journal
    Abbreviation
    Nat. Commun.
    Title
    Nature communications
    ISBN/ISSN
    2041-1723
    Data From Reference
    Genes (8)
    Human Disease Models (1)