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<p>The IAP BRUCE (<i>Birc6</i>) plays multifaceted roles in apoptosis inhibition, DNA repair, and autophagy. Metabolic dysfunction-associated steatotic liver disease (MASLD) and its progressive form, metabolic dysfunction-associated steatohepatitis (MASH), affect up to 30% of the global population, yet their pathogenic mechanisms remain poorly understood. Given BRUCE’s high expression in healthy livers and its downregulation in MASLD/MASH, we investigated its functional role using liver-specific BRUCE-KO and BRUCE/PTEN dual liver-KO (DKO) mouse models. PTEN liver-KO provides a steatotic background and reflects a major etiological factor. By 3 months, BRUCE liver-deficiency alone induces MASLD onset, but when combined with PTEN liver-KO, increases DNA damage, apoptosis, oxidative stress, and MASLD-to-MASH progression, characterized by inflammation and fibrosis. Mechanistically, PTEN liver-KO is known to drive hepatosteatosis through AKT-mediated de novo lipogenesis (DNL) (PTEN-KO → AKT → DNL). However, BRUCE liver-KO impairs mitochondrial fatty acid -oxidation (FAO), respiration and ATP generation (BRUCE→Mitochondria→FAO). This distinct yet complementary mechanism of action leads to a ‘double hit’ of excessive lipid synthesis (PTEN-KO) and impaired lipid clearance (BRUCE-KO), exacerbating steatosis. To elucidate the molecular driver of MASH progression, we found both deficiencies converge on STAT3 activation, a central regulator of inflammation and fibrosis. Further, targeted inhibition of STAT3 with TTI-101 alleviates MASH, establishing a BRUCE/PTEN-STAT3 pathogenic axis. Notably, this axis is conserved in humans, with co-downregulation of BRUCE and PTEN and concurrent STAT3 activation in MASLD/MASH patient specimens. Collectively, these findings establish BRUCE as a key metabolic safeguard against MASLD/MASH, reveal cooperative hepatoprotection by BRUCE/PTEN against MASLD/MASH, and suggest STAT3 inhibition as a targeted therapeutic strategy for BRUCE/PTEN-deficient patients.</p>

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BRUCE liver-KO enhances MASLD/MASH development in the steatotic PTEN-KO background by impairing mitochondrial metabolism and activating STAT3

  • 期刊论文

  • 出版模式：

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  • 发表日期：

    2025年12月11日

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  • Lixiao Che,
  • Camille K. Stevenson,
  • David R. Plas,
  • Jiang Wang,
  • Chunying Du

摘要

The IAP BRUCE (Birc6) plays multifaceted roles in apoptosis inhibition, DNA repair, and autophagy. Metabolic dysfunction-associated steatotic liver disease (MASLD) and its progressive form, metabolic dysfunction-associated steatohepatitis (MASH), affect up to 30% of the global population, yet their pathogenic mechanisms remain poorly understood. Given BRUCE’s high expression in healthy livers and its downregulation in MASLD/MASH, we investigated its functional role using liver-specific BRUCE-KO and BRUCE/PTEN dual liver-KO (DKO) mouse models. PTEN liver-KO provides a steatotic background and reflects a major etiological factor. By 3 months, BRUCE liver-deficiency alone induces MASLD onset, but when combined with PTEN liver-KO, increases DNA damage, apoptosis, oxidative stress, and MASLD-to-MASH progression, characterized by inflammation and fibrosis. Mechanistically, PTEN liver-KO is known to drive hepatosteatosis through AKT-mediated de novo lipogenesis (DNL) (PTEN-KO → AKT → DNL). However, BRUCE liver-KO impairs mitochondrial fatty acid -oxidation (FAO), respiration and ATP generation (BRUCE→Mitochondria→FAO). This distinct yet complementary mechanism of action leads to a ‘double hit’ of excessive lipid synthesis (PTEN-KO) and impaired lipid clearance (BRUCE-KO), exacerbating steatosis. To elucidate the molecular driver of MASH progression, we found both deficiencies converge on STAT3 activation, a central regulator of inflammation and fibrosis. Further, targeted inhibition of STAT3 with TTI-101 alleviates MASH, establishing a BRUCE/PTEN-STAT3 pathogenic axis. Notably, this axis is conserved in humans, with co-downregulation of BRUCE and PTEN and concurrent STAT3 activation in MASLD/MASH patient specimens. Collectively, these findings establish BRUCE as a key metabolic safeguard against MASLD/MASH, reveal cooperative hepatoprotection by BRUCE/PTEN against MASLD/MASH, and suggest STAT3 inhibition as a targeted therapeutic strategy for BRUCE/PTEN-deficient patients.