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自噬和泛素化作为结直肠癌的两大主要参与者:对最新专利的综述。

Autophagy and Ubiquitination as Two Major Players in Colorectal Cancer: A Review on Recent Patents.

机构信息

Clinical Biochemistry Research Center, Basic Health Sciences Institute, Shahrekord University of Medical Sciences, Shahrekord, Iran.

Cellular and Molecular Research Center, Basic Health Sciences Institute, Shahrekord University of Medical Sciences, Shahrekord, Iran.

出版信息

Recent Pat Anticancer Drug Discov. 2020;15(2):143-153. doi: 10.2174/1574892815666200630103626.

DOI:10.2174/1574892815666200630103626
PMID:32603286
Abstract

BACKGROUND

As one of the most commonly diagnosed cancers among men and women, Colorectal Cancer (CRC) leads to high rates of morbidity and mortality across the globe. Recent anti- CRC therapies are now targeting specific signaling pathways involved in colorectal carcinogenesis. Ubiquitin Proteasome System (UPS) and autophagy are two main protein quality control systems, which play major roles in the carcinogenesis of colorectal cancer. A balanced function of these two pathways is necessary for the regulation of cell proliferation and cell death.

OBJECTIVE

In this systematic review, we discuss the available evidence regarding the roles of autophagy and ubiquitination in progression and inhibition of CRC.

METHODS

The search terms "colorectal cancer" or "colon cancer" or "colorectal carcinoma" or "colon carcinoma" in combination with "ubiquitin proteasome" and "autophagy" were searched in PubMed, Web of Science, and Scopus databases, and also Google Patents (https://patents.google .com) from January 2000 to Feb 2020.

RESULTS

The most important factors involved in UPS and autophagy have been investigated. There are many important factors involved in UPS and autophagy but this systematic review shows the studies that have mostly focused on the role of ATG, 20s proteasome and mTOR in CRC, and the more important factors such as ATG8, FIP200, and TIGAR factors that are effective in the regulation of autophagy in CRC cells have not been yet investigated.

CONCLUSION

The most important factors involved in UPS and autophagy such as ATG, 20s proteasome and mTOR, ATG8, FIP200, and TIGAR can be considered in drug therapy for controlling or activating autophagy.

摘要

背景

结直肠癌(CRC)是男性和女性中最常见的癌症之一,在全球范围内导致高发病率和死亡率。目前的抗 CRC 治疗方法针对的是参与结直肠发生的特定信号通路。泛素蛋白酶体系统(UPS)和自噬是两种主要的蛋白质质量控制系统,它们在结直肠癌的发生中起着重要作用。这两种途径的平衡功能对于调节细胞增殖和细胞死亡是必要的。

目的

在本系统评价中,我们讨论了自噬和泛素化在 CRC 进展和抑制中的作用的现有证据。

方法

在 PubMed、Web of Science 和 Scopus 数据库中搜索“结直肠癌”或“结肠癌”或“结直肠腺癌”或“结肠癌”与“泛素蛋白酶体”和“自噬”相结合的检索词,并在 Google Patents(https://patents.google.com)上从 2000 年 1 月到 2020 年 2 月进行搜索。

结果

已经研究了 UPS 和自噬中涉及的最重要因素。UPS 和自噬涉及许多重要因素,但本系统评价显示,大多数研究主要集中在 ATG、20s 蛋白酶体和 mTOR 在 CRC 中的作用,以及在 CRC 细胞中调节自噬的更重要因素,如 ATG8、FIP200 和 TIGAR 因素尚未得到研究。

结论

UPS 和自噬中涉及的最重要因素,如 ATG、20s 蛋白酶体和 mTOR、ATG8、FIP200 和 TIGAR,可以考虑用于控制或激活自噬的药物治疗。

相似文献

1
Autophagy and Ubiquitination as Two Major Players in Colorectal Cancer: A Review on Recent Patents.自噬和泛素化作为结直肠癌的两大主要参与者:对最新专利的综述。
Recent Pat Anticancer Drug Discov. 2020;15(2):143-153. doi: 10.2174/1574892815666200630103626.
2
Ube2v1-mediated ubiquitination and degradation of Sirt1 promotes metastasis of colorectal cancer by epigenetically suppressing autophagy.UBE2V1 介导的 Sirt1 泛素化和降解通过表观遗传抑制自噬促进结直肠癌的转移。
J Hematol Oncol. 2018 Jul 17;11(1):95. doi: 10.1186/s13045-018-0638-9.
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Eat or be eaten: The autophagic plight of inactive 26S proteasomes.适者生存:无活性26S蛋白酶体的自噬困境。
Autophagy. 2015;11(10):1927-8. doi: 10.1080/15548627.2015.1078961.
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Emerging Paradigm of Crosstalk between Autophagy and the Ubiquitin-Proteasome System.自噬与泛素-蛋白酶体系统相互作用的新范式。
Mol Cells. 2017 Dec 31;40(12):897-905. doi: 10.14348/molcells.2017.0226. Epub 2017 Dec 12.
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The ubiquitin-proteasome system in colorectal cancer.结直肠癌中的泛素-蛋白酶体系统。
Biochim Biophys Acta. 2008 Dec;1782(12):800-8. doi: 10.1016/j.bbadis.2008.06.007. Epub 2008 Jun 19.
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mTOR inhibition activates overall protein degradation by the ubiquitin proteasome system as well as by autophagy.mTOR抑制通过泛素蛋白酶体系统以及自噬激活整体蛋白质降解。
Proc Natl Acad Sci U S A. 2015 Dec 29;112(52):15790-7. doi: 10.1073/pnas.1521919112. Epub 2015 Dec 15.
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Pathogenesis of colorectal carcinoma and therapeutic implications: the roles of the ubiquitin-proteasome system and Cox-2.结直肠癌的发病机制及治疗意义:泛素-蛋白酶体系统和环氧化酶-2的作用
J Cell Mol Med. 2007 Mar-Apr;11(2):252-85. doi: 10.1111/j.1582-4934.2007.00032.x.
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The links between AKT and two intracellular proteolytic cascades: ubiquitination and autophagy.AKT与两种细胞内蛋白水解级联反应之间的联系:泛素化和自噬。
Biochim Biophys Acta. 2014 Dec;1846(2):342-52. doi: 10.1016/j.bbcan.2014.07.013. Epub 2014 Aug 7.
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A patent review of the ubiquitin ligase system: 2015-2018.专利审查的泛素连接酶系统:2015-2018。
Expert Opin Ther Pat. 2018 Dec;28(12):919-937. doi: 10.1080/13543776.2018.1549229. Epub 2018 Nov 23.
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The Roles of Ubiquitin-Binding Protein Shuttles in the Degradative Fate of Ubiquitinated Proteins in the Ubiquitin-Proteasome System and Autophagy.泛素结合蛋白穿梭在泛素蛋白酶体系统和自噬中对泛素化蛋白的降解命运中的作用。
Cells. 2019 Jan 10;8(1):40. doi: 10.3390/cells8010040.

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