Mechanism of tumor-suppressive cell competition in flies

被引:20
作者
Kanda, Hiroshi [1 ]
Igaki, Tatsushi [1 ]
机构
[1] Kyoto Univ, Grad Sch Biostudies, Genet Lab, Kyoto, Japan
关键词
cell competition; Drosophila; tumor suppression; ONCOGENIC RAS; EPITHELIAL POLARITY; DROSOPHILA; SENESCENCE; EXPRESSION; HOMOLOG; GROWTH; PROLIFERATION; TUMORIGENESIS; ACTIVATION;
D O I
10.1111/cas.14575
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Oncogenic mutations often trigger antitumor cellular response such as induction of apoptosis or cellular senescence. Studies in the last decade have identified the presence of the third guardian against mutation-induced tumorigenesis, namely "cell competition." Cell competition is a context-dependent cell elimination whereby cells with higher fitness eliminate neighboring cells with lower fitness by inducing cell death. While oncogene-induced apoptosis or oncogene-induced senescence acts as a cell-autonomous tumor suppressor, cell competition protects the tissue from tumorigenesis via cell-cell communication. For instance, inDrosophilaepithelium, oncogenic cells with cell polarity mutations overproliferate and develop into tumors on their own but are eliminated from the tissue when surrounded by wild-type cells. Genetic studies in flies have unraveled that such tumor-suppressive cell competition is regulated by at least three mechanisms: direct cell-cell interaction between polarity-deficient cells and wild-type cells, secreted factors from epithelial cells, and systemic factors from distant organs. Molecular manipulation of tumor-suppressive cell competition could provide a novel therapeutic strategy against human cancers.
引用
收藏
页码:3409 / 3415
页数:7
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