Literature DB >> 32035080

Clinical translation of liver regeneration therapies: A conceptual road map.

Linda E Greenbaum1, Chinweike Ukomadu2, Jan S Tchorz3.   

Abstract

The increasing incidence of severe liver diseases worldwide has resulted in a high demand for curative liver transplantation. Unfortunately, the need for transplants by far eclipses the availability of suitable grafts leaving many waitlisted patients to face liver failure and often death. Routine use of smaller grafts (for example left lobes, split livers) from living or deceased donors could increase the number of life-saving transplants but is often limited by the graft versus recipient weight ratio defining the safety margins that minimize the risk of small for size syndrome (SFSS). SFSS is a severe complication characterized by failure of a small liver graft to regenerate and occurs when a donor graft is insufficient to meet the metabolic demand of the recipient, leading to liver failure as a result of insufficient liver mass. SFSS is not limited to transplantation but can also occur in the setting of hepatic surgical resections, where life-saving large resections of tumors may be limited by concerns of post-surgical liver failure. There are, as yet no available pro-regenerative therapies to enable liver regrowth and thus prevent SFSS. However, there is optimism around targeting factors and pathways that have been identified as regulators of liver regeneration to induce regrowth in vivo and ex vivo for clinical use. In this commentary, we propose a roadmap for developing such pro-regenerative therapy and for bringing it into the clinic. We summarize the clinical indications, preclinical models, pro-regenerative pathways and safety considerations necessary for developing such a drug.
Copyright © 2020 Elsevier Inc. All rights reserved.

Entities:  

Year:  2020        PMID: 32035080     DOI: 10.1016/j.bcp.2020.113847

Source DB:  PubMed          Journal:  Biochem Pharmacol        ISSN: 0006-2952            Impact factor:   5.858


  4 in total

1.  A Mesenchymal-Epithelial Transition Factor-Agonistic Antibody Accelerates Cirrhotic Liver Regeneration and Improves Mouse Survival Following Partial Hepatectomy.

Authors:  Kuai Ma; Weitao Que; Xin Hu; Wen-Zhi Guo; Er-Li Gu; Liang Zhong; Virginia Morello; Manuela Cazzanti; Paolo Michieli; Terumi Takahara; Xiao-Kang Li
Journal:  Liver Transpl       Date:  2021-10-12       Impact factor: 6.112

2.  Trans-activation of eotaxin-1 by Brg1 contributes to liver regeneration.

Authors:  Zhiwen Fan; Ming Kong; Wenhui Dong; Chunlong Dong; Xiulian Miao; Yan Guo; Xingyu Liu; Shuying Miao; Lin Li; Tingting Chen; Yeqing Qu; Fei Yu; Yunfei Duan; Yunjie Lu; Xiaoping Zou
Journal:  Cell Death Dis       Date:  2022-05-25       Impact factor: 9.685

3.  Selective gene expression profiling contributes to a better understanding of the molecular pathways underlying the histological changes observed after RHMVL.

Authors:  Janine Arlt; Sebastian Vlaic; Ronny Feuer; Maria Thomas; Utz Settmacher; Uta Dahmen; Olaf Dirsch
Journal:  BMC Med Genomics       Date:  2022-10-07       Impact factor: 3.622

Review 4.  Wnt/-Catenin Signaling and Liver Regeneration: Circuit, Biology, and Opportunities.

Authors:  Shikai Hu; Satdarshan P Monga
Journal:  Gene Expr       Date:  2021-01-20
  4 in total

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