TY  - JOUR
T1  - YAP disrupts bile acid homeostasis to drive cancer-associated cachexia
JF  - bioRxiv
DO  - 10.64898/2026.02.01.702698
SP  - 2026.02.01.702698
AU  - Webb, Madeline L
AU  - Wong, Mikaela
AU  - Karamalakis, Anthony P
AU  - Liu, Yuchen
AU  - Evason, Kimberley J
AU  - Sun, Kira X
AU  - Brown, Kristin
AU  - Black, Jay R
AU  - Yang, Yingzi
AU  - Cox, Andrew G
Y1  - 2026/01/01
UR  - http://biorxiv.org/content/early/2026/02/03/2026.02.01.702698.abstract
N2  - Cancer-associated cachexia is a severe metabolic syndrome marked by dramatic loss of adipose and muscle mass. Although preclinical models have advanced our understanding of cachexia, there are still no approved therapies due to the limited insights into the mechanisms underlying tissue wasting. Here, we utilise a YAP-driven model of liver cancer in zebrafish, which rapidly develops cachexia, to uncover an evolutionarily conserved role for bile acid disruption in the onset of cachexia. Spatial transcriptomic analysis revealed that YAP induces a bi-lineage cholangiocarcinoma phenotype, which was associated with bile acid dysregulation. Mechanistically, we establish that both bile acid synthesis (via CYP7A1) and signalling through the bile acid receptor TGR5 are essential for cachexia induction. Notably, we find that the promotion of bile acid excretion with odevixibat ameliorates cachexia. Together, our findings reveal an evolutionarily conserved mechanism by which YAP promotes cachexia and suggest a potential therapeutic strategy to treat the syndrome.Competing Interest StatementThe authors have declared no competing interest.National Health and Medical Research Council, https://ror.org/011kf5r70, 1146558, GNT1176650, 2037181Victorian Cancer Agency, MCRF23013GESADame Kate Campbell FellowshipPeter MacCallum Cancer Foundation
ER  -