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Liver-pancreas communication in disease and drug development
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Acta Pharmaceutica Sinica B | 2026, 16(3) : 1250 - 1271
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Acta Pharmaceutica Sinica B | 2026, 16(3): 1250-1271
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Liver-pancreas communication in disease and drug development
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Yan Jia1, Qingtian Zhu2, Qiong Pan3, Guotao Lu2, Jia Xiao4
Affiliations
    1 Department of Gastroenterology, Xiangya Hospital, Central South University, Changsha 410008, China;
    2 Institute of Digestive Diseases, The Affiliated Hospital of Yangzhou University, Yangzhou University, Yangzhou 225000, China;
    3 Cholestatic Liver Diseases Center, The First Affiliated Hospital (Southwest Hospital) of Third Military Medical University (Army Medical University), Chongqing 400038, China;
    4 School of Life and Health Sciences, University of Health and Rehabilitation Sciences, Qingdao 266071, China
doi: 10.1016/j.apsb.2026.01.018
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The liver and pancreas are metabolically intertwined organs whose bidirectional communication is critical for maintaining systemic homeostasis. Dysregulation of this inter-organ crosstalk is a central driver in the pathology of a growing list of prevalent diseases, including metabolic dysfunction-associated steatotic liver disease (MASLD), liver cancer, acute and chronic pancreatitis, and various forms of diabetes. Given the substantial global health burden of these conditions and the lack of effective, Food and Drug Administration (FDA)-approved pharmacological interventions for those diseases, understanding the intricate mechanisms is an urgent and timely endeavor. This review provides a comprehensive synthesis of recent advancements in deciphering the molecular basis of liver-pancreas communication. We explore the multifaceted signaling networks involved, including the roles of liver-derived hepatokines, pancreas-derived hormones, extracellular vesicles, and metabolic exchanges. This axis is further integrated within broader systemic networks involving the gut, neuronal system, adipose tissue, and skeletal muscle. While clinical trials targeting this communication show promise (e.g., FGF21- and bile acid-related drugs), significant challenges remain, particularly the lack of FDA-approved pharmacological treatments for alcohol-associated liver disease (ALD), and acute/chronic pancreatitis. Future research must elucidate specific signaling pathways, identify novel pancreas-derived factors, and develop innovative therapeutic strategies. In particular, small molecule drug discovery based on polypharmacology, for these complex metabolic and organ-specific diseases.
Liver  /  Pancreas  /  Hepatokine  /  Hormones  /  Extracellular vesicles  /  Communication  /  Organ crosstalk  /  Drug development
Yan Jia, Qingtian Zhu, Qiong Pan, Guotao Lu, Jia Xiao. Liver-pancreas communication in disease and drug development[J]. Acta Pharmaceutica Sinica B, 2026 , 16 (3) : 1250 -1271 . DOI: 10.1016/j.apsb.2026.01.018
Year 2026 volume 16 Issue 3
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doi: 10.1016/j.apsb.2026.01.018
  • Receive Date:2025-08-07
  • Online Date:2026-09-17
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  • Received:2025-08-07
  • Revised:2025-11-03
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表12种不同金属材料的力学参数

Family
属数
Number of
genus
种数
Number of
species
占总种数比例
Percentage of
total species (%)

Genus
种数
Number of
species
占总种数比例
Percentage of total
species (%)
鹅膏菌科Amanitaceae 2 11 5.26 鹅膏菌属 Amanita 10 4.78
小菇科 Mycenaceae 2 12 5.74 丝盖伞属 Inocybe 5 2.39
多孔菌科 Polyporaceae 8 14 6.70 蜡蘑属 Laccaria 5 2.39
红菇科 Russulaceae 3 23 11.00 小皮伞属 Marasmius 6 2.87
小菇属 Mycena 11 5.26
光柄菇属 Pluteus 5 2.39
红菇属 Russula 17 8.13
栓菌属 Trametes 5 2.39
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