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垂体肿瘤转化基因 1/Delta 样非经典 Notch 配体 1 在慢性肝病中的信号转导。

Pituitary Tumor-Transforming Gene 1/Delta like Non-Canonical Notch Ligand 1 Signaling in Chronic Liver Diseases.

机构信息

Biochemistry and Molecular Genetics Service, Hospital Clínic Universitari, 08036 Barcelona, Spain.

Institut d'Investigacions Biomèdiques August Pi i Sunyer (IDIBAPS), Centro de Investigación Biomédica en Red de Enfermedades Hepáticas y Digestivas (CIBEReHD), 08036 Barcelona, Spain.

出版信息

Int J Mol Sci. 2022 Jun 21;23(13):6897. doi: 10.3390/ijms23136897.

Abstract

The management of chronic liver diseases (CLDs) remains a challenge, and identifying effective treatments is a major unmet medical need. In the current review we focus on the pituitary tumor transforming gene (PTTG1)/delta like non-canonical notch ligand 1 (DLK1) axis as a potential therapeutic target to attenuate the progression of these pathological conditions. PTTG1 is a proto-oncogene involved in proliferation and metabolism. PTTG1 expression has been related to inflammation, angiogenesis, and fibrogenesis in cancer and experimental fibrosis. On the other hand, DLK1 has been identified as one of the most abundantly expressed PTTG1 targets in adipose tissue and has shown to contribute to hepatic fibrosis by promoting the activation of hepatic stellate cells. Here, we extensively analyze the increasing amount of information pointing to the PTTG1/DLK1 signaling pathway as an important player in the regulation of these disturbances. These data prompted us to hypothesize that activation of the PTTG1/DLK1 axis is a key factor upregulating the tissue remodeling mechanisms characteristic of CLDs. Therefore, disruption of this signaling pathway could be useful in the therapeutic management of CLDs.

摘要

慢性肝脏疾病(CLDs)的管理仍然是一个挑战,寻找有效的治疗方法是一个主要的未满足的医学需求。在目前的综述中,我们重点关注垂体肿瘤转化基因(PTTG1)/δ样非经典 Notch 配体 1(DLK1)轴作为潜在的治疗靶点,以减轻这些病理状况的进展。PTTG1 是一种参与增殖和代谢的原癌基因。PTTG1 的表达与癌症和实验性纤维化中的炎症、血管生成和纤维化有关。另一方面,DLK1 已被确定为脂肪组织中表达最丰富的 PTTG1 靶标之一,并通过促进肝星状细胞的激活,显示出对肝纤维化的贡献。在这里,我们广泛分析了越来越多的信息,这些信息表明 PTTG1/DLK1 信号通路是调节这些紊乱的重要因素。这些数据促使我们假设 PTTG1/DLK1 轴的激活是上调 CLD 特征性组织重塑机制的关键因素。因此,破坏这种信号通路可能对 CLD 的治疗管理有用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/92eb/9267054/b3e95159a8d2/ijms-23-06897-g001.jpg

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