Targeting Legumain As a Novel Therapeutic Strategy in Cancers

被引:50
|
作者
Mai, Chun-Wai [1 ]
Chung, Felicia Fei-Lei [2 ]
Leong, Chee-Onn [1 ,2 ]
机构
[1] Int Med Univ, Sch Pharm, 126 Jalan 19-155B, Kuala Lumpur 57000, Malaysia
[2] Int Med Univ, Ctr Canc & Stem Cell Res, Kuala Lumpur 57000, Malaysia
关键词
Legumain; cancer; tumor microenvironment; vaccine; azo-peptide; small molecules; prodrug; TUMOR-ASSOCIATED MACROPHAGES; ASPARAGINYL ENDOPEPTIDASE; IN-VITRO; OPISTHORCHIS-VIVERRINI; BIOLOGICAL VARIABLES; SCHISTOSOMA-MANSONI; PROTEINASE LEGUMAIN; CELL-PROLIFERATION; MAMMALIAN LEGUMAIN; GENE-EXPRESSION;
D O I
10.2174/1389450117666161216125344
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Background: Recent reports indicate that the tumor microenvironment plays a pivotal role in cancer development and progression, leading to a paradigm shift in the way cancer is studied and targeted. In contrast to traditional approaches, where only tumor cells are targeted for the treatment, an emerging approach is to develop therapeutics which target the tumor microenvironment while complementing or enhancing current treatments. Legumain (LGMN) is a newly identified target which is highly expressed in the tumor microenvironment and in tumor cells, and holds potential both as a biomarker and as a therapeutic target. Conclusion: This review will be the first to summarize the expression of LGMN in common cancers, as well as its roles in tumorigenesis and metastasis. This review also discusses the current developments and future prospects of targeting LGMN through the development of DNA vaccines, azopeptides, small molecule inhibitors and LGMN activated prodrugs, highlighting the potential of LGMN as a target for cancer therapeutics.
引用
收藏
页码:1259 / 1268
页数:10
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