Beyond cytokinesis: the emerging roles of CEP55 in tumorigenesis

被引:114
作者
Jeffery, J. [1 ]
Sinha, D. [1 ,2 ]
Srihari, S. [3 ]
Kalimutho, M. [1 ]
Khanna, K. K. [1 ]
机构
[1] QIMR Berghofer Med Res Inst, Signal Transduct Lab, 300 Hcrston Rd, Brisbane, Qld, Australia
[2] Griffith Univ, Sch Nat Sci, Brisbane, Qld 4111, Australia
[3] Univ Queensland, Inst Mol Biosci, Brisbane, Qld, Australia
基金
英国医学研究理事会;
关键词
GENE-EXPRESSION PROFILES; SQUAMOUS-CELL CARCINOMA; BREAST-CANCER; ESCRT-III; PLK1-DEPENDENT PHOSPHORYLATION; INTERCELLULAR BRIDGES; CENTROSOMAL PROTEIN; UP-REGULATION; KINASE; MIDBODY;
D O I
10.1038/onc.2015.128
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
CEP55 was initially identified as a pivotal component of abscission, the final stage of cytokinesis, serving to regulate the physical separation of two daughter cells. Over the past 10 years, several studies have illuminated additional roles for CEP55 including regulating the PI3K/AKT pathway and midbody fate. Concurrently, CEP55 has been studied in the context of cancers including those of the breast, lung, colon and liver. CEP55 overexpression has been found to significantly correlate with tumor stage, aggressiveness, metastasis and poor prognosis across multiple tumor types and therefore has been included as part of several prognostic 'gene signatures' for cancer. Here by discussing in depth the functions of CEP55 across different effector pathways, and also its roles as a biomarker and driver of tumorigenesis, we assemble an exhaustive review, thus commemorating a decade of research on CEP55.
引用
收藏
页码:683 / 690
页数:8
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