SEMA5A-PLXNB3轴通过增强沃伯格效应促进PDAC肝转移灶生长

IF 3.5 3区 医学 Q2 IMMUNOLOGY Journal of Immunology Research Pub Date : 2023-01-27 eCollection Date: 2023-01-01 DOI:10.1155/2023/3274467
Kun Wang, Min He, Xin Fan, Jian Zhou, Jian Yang, Lin Wang, Zhihong Zhao, Chun Dai, Zixiang Zhang
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引用次数: 0

摘要

胰腺腺癌(PDAC)肝转移患者因病程短、死亡率高而预后不良。肝转移龛中存在复杂的肿瘤微环境(TME),而肿瘤相关巨噬细胞(TAMs)在转移灶的生成和生长中发挥着重要作用。我们发现,M2型TAM衍生的SEMA5A可与其肿瘤细胞表达的受体PLXNB3结合,促进肿瘤细胞的增殖和生长。我们利用PDAC患者肝转移样本、脾内注射小鼠模型和Kras G12D/Trp53 R172H/Pdx1-Cre(KPC)小鼠模型进行了体内研究。在机制研究中,我们发现 SEMA5A-PLXNB3 轴可通过增强有氧糖酵解(称为沃伯格效应)实现肿瘤细胞的增殖和存活。针对这一轴心可能是治疗无法切除的肝转移的 PDAC 患者的一种潜在方法。
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SEMA5A-PLXNB3 Axis Promotes PDAC Liver Metastasis Outgrowth through Enhancing the Warburg Effect.

Patients bearing liver metastasis of pancreatic adeno carcinoma (PDAC) suffer from poor prognosis due to its short duration and high mortality. Complex tumor microenvironment (TME) exists in liver metastatic niches, and tumor-associated macrophages (TAMs) have play vital roles in metastasis generation and outgrowth. We have discovered that M2 type TAM-derived SEMA5A could bind to its tumor cell-expressed receptor PLXNB3 to promote tumor cell proliferation and outgrowth. We utilized liver metastasis samples of PDAC patients, intrasplenic injection mouse models, and Kras G12D/Trp53 R172H/Pdx1-Cre (KPC) mouse models for in vivo study. In mechanism investigation, we have discovered that SEMA5A-PLXNB3 axis could achieve tumor cell proliferation and survival via enhancing aerobic glycolysis termed as the Warburg effects. Targeting this axis may be a potential therapeutic approach for PDAC patients with unresectable liver metastasis.

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来源期刊
CiteScore
6.90
自引率
2.40%
发文量
423
审稿时长
15 weeks
期刊介绍: Journal of Immunology Research is a peer-reviewed, Open Access journal that provides a platform for scientists and clinicians working in different areas of immunology and therapy. The journal publishes research articles, review articles, as well as clinical studies related to classical immunology, molecular immunology, clinical immunology, cancer immunology, transplantation immunology, immune pathology, immunodeficiency, autoimmune diseases, immune disorders, and immunotherapy.
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