Sds22/PP1 links epithelial integrity and tumor suppression via regulation of myosin II and JNK signaling

被引:24
作者
Jiang, Y. [1 ]
Scott, K. L. [1 ]
Kwak, S-J [2 ]
Chen, R. [1 ,3 ,4 ]
Mardon, G. [1 ,2 ,3 ,4 ,5 ,6 ]
机构
[1] Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USA
[2] Baylor Coll Med, Dept Pathol, Houston, TX 77030 USA
[3] Baylor Coll Med, Program Dev Biol, Houston, TX 77030 USA
[4] Baylor Coll Med, Human Genome Sequencing Ctr, Houston, TX 77030 USA
[5] Baylor Coll Med, Dept Neurosci, Houston, TX 77030 USA
[6] Baylor Coll Med, Dept Ophthalmol, Houston, TX 77030 USA
关键词
tumor suppressor; epithelial integrity; cell invasion; sds22; protein phosphatase 1; PROTEIN PHOSPHATASE-1; CELL POLARITY; NONMUSCLE MYOSIN; MATRIX METALLOPROTEINASES; DROSOPHILA-MELANOGASTER; NEURAL DEVELOPMENT; INDUCED APOPTOSIS; GENETIC MOSAICS; IMAGINAL DISCS; CANCER;
D O I
10.1038/onc.2011.46
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
Loss of epithelial integrity often correlates with the progression of malignant tumors. Sds22, a regulatory subunit of protein phosphatase 1 (PP1), has recently been linked to regulation of epithelial polarity in Drosophila. However, its role in tumorigenesis remains obscure. In this study, using Drosophila imaginal tissue as an in vivo model system, we show that sds22 is a new potential tumor suppressor gene in Drosophila. Without sds22, cells lose epithelial architecture, and become invasive and tumorigenic when combined with Ras overexpression; conversely, sds22 overexpression can largely suppress tumorigenic growth of Ras(V12)scrib(-/-) mutant cells. Mechanistically, we show that sds22 prevents cell invasion and metastasis by inhibiting myosin II and Jun N-terminal kinase (JNK) activity downstream of PP1. Loss of this inhibition causes cells to lose epithelial organization and promotes cell invasion. Finally, human Sds22 is focally deleted and downregulated in multiple carcinomas, and this downregulation correlates with tumor progression, suggesting that sds22 inactivation may contribute to tumorigenesis and metastatic potential in human cancers via a similar mechanism. Oncogene (2011) 30, 3248-3260; doi:10.1038/onc.2011.46; published online 14 March 2011
引用
收藏
页码:3248 / 3260
页数:13
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