共 80 条
Pathomimetic cancer avatars for live-cell imaging of protease activity
被引:4
作者:
Ji, Kyungmin
[1
]
Heyza, Joshua
[2
,3
]
Cavallo-Medved, Dora
[1
,4
]
Sloane, Bonnie F.
[1
,2
,3
,4
]
机构:
[1] Wayne State Univ, Sch Med, Dept Pharmacol, 540 E Canfield, Detroit, MI 48201 USA
[2] Wayne State Univ, Sch Med, Canc Biol Grad Program, 540 E Canfield, Detroit, MI 48201 USA
[3] Wayne State Univ, Sch Med, Dept Oncol, Detroit, MI 48201 USA
[4] Univ Windsor, Dept Biol Sci, 401 Sunset Ave, Windsor, ON N9B 3P4, Canada
来源:
基金:
美国国家卫生研究院;
关键词:
Protease;
Live-cell imaging;
Breast cancer;
Tumor microenvironment;
3D models;
ACTIVITY-BASED PROBES;
B PROMOTES PROGRESSION;
CATHEPSIN-B;
BREAST-CANCER;
MATRIX METALLOPROTEINASES;
ORGANOID CULTURES;
DRUG-RESISTANCE;
ENZYME-ACTIVITY;
MELANOMA-CELLS;
METASTASIS;
D O I:
10.1016/j.biochi.2015.09.015
中图分类号:
Q5 [生物化学];
Q7 [分子生物学];
学科分类号:
071010 ;
081704 ;
摘要:
Proteases are essential for normal physiology as well as multiple diseases, e.g., playing a causative role in cancer progression, including in tumor angiogenesis, invasion, and metastasis. Identification of dynamic alterations in protease activity may allow us to detect early stage cancers and to assess the efficacy of anti-cancer therapies. Despite the clinical importance of proteases in cancer progression, their functional roles individually and within the context of complex protease networks have not yet been well defined. These gaps in our understanding might be addressed with: 1) accurate and sensitive tools and methods to directly identify changes in protease activities in live cells, and 2) pathomimetic avatars for cancer that recapitulate in vitro the tumor in the context of its cellular and non-cellular microenvironment. Such avatars should be designed to facilitate mechanistic studies that can be translated to animal models and ultimately the clinic. Here, we will describe basic principles and recent applications of live-cell imaging for identification of active proteases. The avatars optimized by our laboratory are three-dimensional (3D) human breast cancer models in a matrix of reconstituted basement membrane (rBM). They are designated mammary architecture and microenvironment engineering (MAME) models as they have been designed to mimic the structural and functional interactions among cell types in the normal and cancerous human breast. We have demonstrated the usefulness of these pathomimetic avatars for following dynamic and temporal changes in cell:cell interactions and quantifying changes in protease activity associated with these interactions in real-time (4D). We also briefly describe adaptation of the avatars to custom-designed and fabricated tissue architecture and microenvironment engineering (TAME) chambers that enhance our ability to analyze concomitant changes in the malignant phenotype and the associated tumor microenvironment. (C) 2015 Published by Elsevier B.V.
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页码:68 / 76
页数:9
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