In Vivo Identification of Regulators of Cell Invasion Across Basement Membranes

被引:47
|
作者
Matus, David Q. [1 ]
Li, Xiao-Yan [2 ,3 ]
Durbin, Sarah [1 ]
Agarwal, Daniel [1 ]
Chi, Qiuyi [1 ]
Weiss, Stephen J. [2 ,3 ]
Sherwood, David R. [1 ]
机构
[1] Duke Univ, Dept Biol, Durham, NC 27708 USA
[2] Univ Michigan, Dept Internal Med, Div Mol Med & Genet, Ann Arbor, MI 48109 USA
[3] Univ Michigan, Inst Life Sci, Ann Arbor, MI 48109 USA
关键词
C-ELEGANS; CAENORHABDITIS-ELEGANS; ANCHOR-CELL; EXTRACELLULAR-MATRIX; CANCER METASTASIS; PROTOONCOGENE; EXPRESSION; INDUCTION; PROGRAMS; MT1-MMP;
D O I
10.1126/scisignal.2000654
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
Cell invasion through basement membranes during development, immune surveillance, and metastasis remains poorly understood. To gain further insight into this key cellular behavior, we performed an in vivo screen for regulators of cell invasion through basement membranes, using the simple model of Caenorhabditis elegans anchor cell invasion, and identified 99 genes that promote invasion, including the genes encoding the chaperonin complex cct. Notably, most of these genes have not been previously implicated in invasive cell behavior. We characterized members of the cct complex and 11 other gene products, determining the distinct aspects of the invasive cascade that they regulate, including formation of a specialized invasive cell membrane and its ability to breach the basement membrane. RNA interference-mediated knockdown of the human orthologs of cct-5 and lit-1, which had not previously been implicated in cell invasion, reduced the invasiveness of metastatic carcinoma cells, suggesting that a conserved genetic program underlies cell invasion. These results increase our understanding of the genetic underpinnings of cell invasion and also provide new potential therapeutic targets to limit this behavior.
引用
收藏
页数:9
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