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Opportunities and Challenges of Nanoparticles in Digestive Tumours as Anti-Angiogenic Therapies.

作者信息

Yang Zhengyang, Deng Wei, Zhang Xiao, An Yongbo, Liu Yishan, Yao Hongwei, Zhang Zhongtao

机构信息

Department of General Surgery, Beijing Friendship Hospital, Capital Medical University and National Clinical Research Center for Digestive Diseases, Beijing, China.

出版信息

Front Oncol. 2022 Jan 10;11:789330. doi: 10.3389/fonc.2021.789330. eCollection 2021.


DOI:10.3389/fonc.2021.789330
PMID:35083147
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8784389/
Abstract

Digestive tumours, a common kind of malignancy worldwide, have recently led to the most tumour-related deaths. Angiogenesis, the process of forming novel blood vessels from pre-existing vessels, is involved in various physiological and pathological processes in the body. Many studies suggest that abnormal angiogenesis plays an important role in the growth, progression, and metastasis of digestive tumours. Therefore, anti-angiogenic therapy is considered a promising target for improving therapeutic efficacy. Traditional strategies such as bevacizumab and regorafenib can target and block the activity of proangiogenic factors to treat digestive tumours. However, due to resistance and some limitations, such as poor pharmacokinetics, their efficacy is not always satisfactory. In recent years, nanotechnology-based anti-angiogenic therapies have emerged as a new way to treat digestive tumours. Compared with commonly used drugs, nanoparticles show great potential in tumour targeted delivery, controlled drug release, prolonged cycle time, and increased drug bioavailability. Therefore, anti-angiogenic nanoparticles may be an effective complementary therapy to treat digestive tumours. In this review, we outline the different mechanisms of angiogenesis, the effects of nanoparticles on angiogenesis, and their biomedical applications in various kinds of digestive tumours. In addition, the opportunities and challenges are briefly discussed.

摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d938/8784389/2e2c2136f387/fonc-11-789330-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d938/8784389/738ed872c65e/fonc-11-789330-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d938/8784389/55211848583c/fonc-11-789330-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d938/8784389/2e2c2136f387/fonc-11-789330-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d938/8784389/738ed872c65e/fonc-11-789330-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d938/8784389/55211848583c/fonc-11-789330-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d938/8784389/2e2c2136f387/fonc-11-789330-g003.jpg

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本文引用的文献

[1]
An iRGD peptide conjugated heparin nanocarrier for gastric cancer therapy.

RSC Adv. 2018-8-24

[2]
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Front Oncol. 2021-9-16

[3]
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J Control Release. 2021-11-10

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Nanoscale. 2021-9-2

[5]
Coordination and Redox Dual-Responsive Mesoporous Organosilica Nanoparticles Amplify Immunogenic Cell Death for Cancer Chemoimmunotherapy.

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Curr Oncol. 2021-5-24

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Eur J Pharmacol. 2021-6-5

[9]
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Nat Rev Cardiol. 2021-6

[10]
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Bioact Mater. 2020-12-26

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