Dissecting Social Cell Biology and Tumors Using Drosophila Genetics

被引:46
|
作者
Pastor-Pareja, Jose Carlos [1 ,2 ]
Xu, Tian [2 ,3 ]
机构
[1] Tsinghua Univ, Sch Life Sci, Beijing 100084, Peoples R China
[2] Yale Univ, Sch Med, Howard Hughes Med Inst, Dept Genet, New Haven, CT 06519 USA
[3] Fudan Univ, Sch Life Sci, Inst Dev Biol & Mol Med, Fudan Yale Biomed Res Ctr, Shanghai 20043, Peoples R China
来源
关键词
cell competition; compensatory proliferation; interclonal cooperation; basement membrane; tumor immunity; JNK; SOMATIC STEM-CELLS; N-TERMINAL KINASE; COMPENSATORY PROLIFERATION; HIPPO PATHWAY; IMAGINAL DISCS; SUPPRESSOR GENES; MOSAIC ANALYSIS; ONCOGENIC RAS; BACTERIAL-INFECTION; TISSUE OVERGROWTH;
D O I
10.1146/annurev-genet-110711-155414
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Cancer was seen for a long time as a strictly cell-autonomous process in which oncogenes and tumor-suppressor mutations drive clonal cell expansions. Research in the past decade, however, paints a more integrative picture of communication and interplay between neighboring cells in tissues. It is increasingly clear as well that tumors, far from being homogenous lumps of cells, consist of different cell types that function together as complex tissue-level communities. The repertoire of interactive cell behaviors and the quantity of cellular players involved call for a social cell biology that investigates these interactions. Research into this social cell biology is critical for understanding development of normal and tumoral tissues. Such complex social cell biology interactions can be parsed in Drosophila. Techniques in Drosophila for analysis of gene function and clonal behavior allow us to generate tumors and dissect their complex interactive biology with cellular resolution. Here, we review recent Drosophila research aimed at understanding tissue-level biology and social cell interactions in tumors, highlighting the principles these studies reveal.
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收藏
页码:51 / 74
页数:24
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