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针对缺氧机制治疗胰腺癌的新型疗法。

Novel therapies targeting hypoxia mechanism to treat pancreatic cancer.

作者信息

Luo Wenhao, Qiu Jiangdong, Zheng Lianfang, Zhang Taiping

机构信息

Department of General Surgery, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing 100730, China.

Department of Nuclear Medicine, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing 100730, China.

出版信息

Chin J Cancer Res. 2021 Apr 30;33(2):216-231. doi: 10.21147/j.issn.1000-9604.2021.02.09.

DOI:10.21147/j.issn.1000-9604.2021.02.09
PMID:34158741
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8181875/
Abstract

Pancreatic cancer (PC) is one of the deadliest malignancies. The high mortality rate of PC largely results from delayed diagnosis and early metastasis. Therefore, identifying novel treatment targets for patients with PC is urgently required to improve survival rates. A major barrier to successful treatment of PC is the presence of a hypoxic tumor microenvironment, which is associated with poor prognosis, treatment resistance, increased invasion and metastasis. Recent studies have identified a number of novel molecules and pathways in PC cells that promote cancer cells progression under hypoxic conditions, which may provide new therapy strategies to inhibit the development and metastasis of PC. This review summarizes the latest research of hypoxia in PC and provides an overview of how the current therapies have the capacity to overcome hypoxia and improve PC patient treatment. These findings will eventually provide guidance for future PC management and clinical trials and hopefully improve the survival of patients with PC.

摘要

胰腺癌(PC)是最致命的恶性肿瘤之一。PC的高死亡率主要源于诊断延迟和早期转移。因此,迫切需要为PC患者确定新的治疗靶点以提高生存率。PC成功治疗的一个主要障碍是存在缺氧的肿瘤微环境,这与预后不良、治疗耐药性、侵袭和转移增加有关。最近的研究已经在PC细胞中鉴定出许多新的分子和途径,它们在缺氧条件下促进癌细胞进展,这可能为抑制PC的发展和转移提供新的治疗策略。本综述总结了PC中缺氧的最新研究,并概述了当前疗法如何有能力克服缺氧并改善PC患者的治疗。这些发现最终将为未来的PC管理和临床试验提供指导,并有望提高PC患者的生存率。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/87bd/8181875/74fe0dbe77ac/cjcr-33-2-216-4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/87bd/8181875/f97e9fc56925/cjcr-33-2-216-1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/87bd/8181875/77e1b6e542f1/cjcr-33-2-216-2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/87bd/8181875/f8becda8654d/cjcr-33-2-216-3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/87bd/8181875/74fe0dbe77ac/cjcr-33-2-216-4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/87bd/8181875/f97e9fc56925/cjcr-33-2-216-1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/87bd/8181875/77e1b6e542f1/cjcr-33-2-216-2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/87bd/8181875/f8becda8654d/cjcr-33-2-216-3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/87bd/8181875/74fe0dbe77ac/cjcr-33-2-216-4.jpg

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本文引用的文献

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J Cell Physiol. 2021 Mar;236(3):2087-2098. doi: 10.1002/jcp.29995. Epub 2020 Aug 4.
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MiR-301a transcriptionally activated by HIF-2α promotes hypoxia-induced epithelial-mesenchymal transition by targeting TP63 in pancreatic cancer.缺氧诱导因子 2α转录激活 miR-301a 通过靶向 TP63 促进胰腺癌缺氧诱导的上皮-间充质转化。
World J Gastroenterol. 2020 May 21;26(19):2349-2373. doi: 10.3748/wjg.v26.i19.2349.
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Curcumin inhibits pancreatic cancer cell invasion and EMT by interfering with tumor‑stromal crosstalk under hypoxic conditions via the IL‑6/ERK/NF‑κB axis.
胰腺癌流行病学:新版本,新视野。
Chin J Cancer Res. 2023 Oct 30;35(5):438-450. doi: 10.21147/j.issn.1000-9604.2023.05.03.
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Prognostic Stratification Based on HIF-1 Signaling for Evaluating Hypoxic Status and Immune Infiltration in Pancreatic Ductal Adenocarcinomas.基于 HIF-1 信号的预后分层评估胰腺导管腺癌的缺氧状态和免疫浸润。
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姜黄素通过 IL-6/ERK/NF-κB 轴在缺氧条件下干扰肿瘤-基质串扰,从而抑制胰腺癌细胞侵袭和 EMT。
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Fibroblast growth factor 19 alleviates palmitic acid-induced mitochondrial dysfunction and oxidative stress via the AMPK/PGC-1α pathway in skeletal muscle.成纤维细胞生长因子 19 通过 AMPK/PGC-1α 通路缓解棕榈酸诱导的骨骼肌线粒体功能障碍和氧化应激。
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IL-37/ STAT3/ HIF-1α negative feedback signaling drives gemcitabine resistance in pancreatic cancer.IL-37/STAT3/HIF-1α 负反馈信号通路驱动胰腺癌对吉西他滨产生耐药性。
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A nomogram to preoperatively predict 1-year disease-specific survival in resected pancreatic cancer following neoadjuvant chemoradiation therapy.一种用于术前预测新辅助放化疗后切除的胰腺癌1年疾病特异性生存率的列线图。
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