Live-cell imaging of tumor proteolysis: Impact of cellular and non-cellular microenvironment

被引:20
作者
Rothberg, Jennifer M. [1 ,2 ]
Sameni, Mansoureh
Moin, Kamiar [2 ]
Sloane, Bonnie F. [2 ]
机构
[1] Wayne State Univ, Sch Med, Dept Pharmacol, Detroit, MI 48201 USA
[2] Wayne State Univ, Barbara Ann Karmanos Canc Inst, Detroit, MI 48201 USA
来源
BIOCHIMICA ET BIOPHYSICA ACTA-PROTEINS AND PROTEOMICS | 2012年 / 1824卷 / 01期
基金
美国国家卫生研究院;
关键词
Lysosomal proteases; Proteolytic networks; Functional imaging; 3D culture; Organotypic models; Tumor microenvironment; MATRIX-METALLOPROTEINASE INHIBITORS; BREAST-CANCER DEVELOPMENT; CATHEPSIN-B; EXTRACELLULAR-MATRIX; MAMMARY-GLAND; PLASMINOGEN-ACTIVATOR; HOST MICROENVIRONMENT; IN-VIVO; PROMOTES PROGRESSION; ELEVATED EXPRESSION;
D O I
10.1016/j.bbapap.2011.07.025
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
Our laboratory has had a longstanding interest in how the interactions between tumors and their microenvironment affect malignant progression. Recently, we have focused on defining the proteolytic pathways that function in the transition of breast cancer from the pre-invasive lesions of ductal carcinoma in situ (DCIS) to invasive ductal carcinomas (IDCs). We use live-cell imaging to visualize, localize and quantify proteolysis as it occurs in real-time and thereby have established roles for lysosomal cysteine proteases both pericellularly and intracellularly in tumor proteolysis. To facilitate these studies, we have developed and optimized 3D organotypic co-culture models that recapitulate the in vivo interactions of mammary epithelial cells or tumor cells with stromal and inflammatory cells. Here we will discuss the background that led to our present studies as well as the techniques and models that we employ. This article is part of a Special Issue entitled: Proteolysis 50 years after the discovery of lysosome. (C) 2011 Elsevier B.V. All rights reserved.
引用
收藏
页码:123 / 132
页数:10
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