Centrosomal-associated Proteins: Potential therapeutic targets for solid tumors?

被引:18
作者
Luan, Yi [1 ]
Li, Mingli [2 ]
Zhao, Yi [1 ]
Li, Qianqian [3 ]
Wen, Jia [4 ]
Gao, Siqi [5 ]
Yang, Yang [1 ]
机构
[1] Zhengzhou Univ, Affiliated Hosp 1, Translat Med Ctr, Zhengzhou 450052, Peoples R China
[2] Zhengzhou Univ, Dept Neurol, Affiliated Hosp 1, Zhengzhou 450052, Peoples R China
[3] Zhengzhou Univ, Affiliated Hosp 1, Dept Obstet & Gynecol, Genet & Prenatal Diag Ctr, Zhengzhou 450052, Peoples R China
[4] Zhengzhou Univ, Affiliated Hosp 1, Dept Osteol, Zhengzhou 450052, Peoples R China
[5] Hebei North Univ, Inst Microcirculat, Zhangjiakou 075000, Peoples R China
基金
中国国家自然科学基金; 中国博士后科学基金;
关键词
Centrosome; Cancer; Structure; Centrosomal-associated Proteins; Therapeutic targets; PAPILLOMAVIRUS TYPE-16 E6; CELL-CYCLE; CHROMOSOMAL INSTABILITY; AURORA-A; CENTRIOLE BIOGENESIS; PLK4; INHIBITOR; BREAST-CANCER; KINASE; DUPLICATION; OVEREXPRESSION;
D O I
10.1016/j.biopha.2021.112292
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
The centrosome is a special organelle in human cells and an organizing unit for microtubules and signaling molecules. In addition, the centrosome is tightly restricted during the cell cycle and forms the basal body of the cilia in ciliated cells. Centrosome abnormality is frequently observed in malignant tumors. The dysregulation of centrosome-associated proteins leads to multipolar mitosis, aneuploidy, and nondirected cell migration, and therefore promotes cancer progression. The overduplication of primary centrosome and the accumulation of chromosome, comprise the majority cause of chromosomal mis-segregation in cancer cells. This review discusses the structure and function of the centrosome and the role of its associated proteins in the progression of solid tumors. We summarized the effects of centrosome amplification abnormalities and other centrosome-related phenotypes on tumors. The mechanism of the delineation of centrosome amplification with tumor malignancy remains to be decided. A better understanding of centrosome abnormality in tumorigenesis may be useful to screen novel therapeutic strategies for the treatment of solid tumors.
引用
收藏
页数:9
相关论文
共 119 条
[1]   Coordination of Centrosome Homeostasis and DNA Repair Is Intact in MCF-7 and Disrupted in MDA-MB 231 Breast Cancer Cells [J].
Acu, Ilie D. ;
Liu, Tieju ;
Suino-Powell, Kelly ;
Mooney, Steven M. ;
D'Assoro, Antonino B. ;
Rowland, Nicholas ;
Muotri, Alysson R. ;
Correa, Ricardo G. ;
Niu, Yun ;
Kumar, Rajiv ;
Salisbury, Jeffrey L. .
CANCER RESEARCH, 2010, 70 (08) :3320-3328
[2]   Regulation of APC/C-Cdh1 and Its Function in Neuronal Survival [J].
Almeida, Angeles .
MOLECULAR NEUROBIOLOGY, 2012, 46 (03) :547-554
[3]   Design and synthesis of novel benzoxazole analogs as Aurora B kinase inhibitors [J].
An, Ying ;
Lee, Eun ;
Yu, Yeongji ;
Yun, Jieun ;
Lee, Myeong Youl ;
Kang, Jong Soon ;
Kim, Woo-Young ;
Jeon, Raok .
BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 2016, 26 (13) :3067-3072
[4]   Structure and duplication of the centrosome [J].
Azimzadeh, Juliette ;
Bornens, Michel .
JOURNAL OF CELL SCIENCE, 2007, 120 (13) :2139-2142
[5]   Compartmentalization of Photoreceptor Sensory Cilia [J].
Barnes, Cassandra L. ;
Malhotra, Himanshu ;
Calvert, Peter D. .
FRONTIERS IN CELL AND DEVELOPMENTAL BIOLOGY, 2021, 9
[6]   Aurora Kinase inhibitors: Current Status and Outlook [J].
Bavetsias, Vassilios ;
Linardopoulos, Spiros .
FRONTIERS IN ONCOLOGY, 2015, 5
[7]   Centrosome biogenesis and function: centrosomics brings new understanding [J].
Bettencourt-Dias, Monica ;
Glover, David M. .
NATURE REVIEWS MOLECULAR CELL BIOLOGY, 2007, 8 (06) :451-463
[8]   Covalent capture of kinase-specific phosphopeptides reveals Cdk1-cyclin B substrates [J].
Blethrow, Justin D. ;
Glavy, Joseph S. ;
Morgan, David O. ;
Shokat, Kevan M. .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2008, 105 (05) :1442-1447
[9]   Aurora kinases: New targets for cancer therapy [J].
Carvajal, Richard D. ;
Tse, Archie ;
Schwartz, Gary K. .
CLINICAL CANCER RESEARCH, 2006, 12 (23) :6869-6875
[10]   Ift88 regulates Hedgehog signaling, Sfrp5 expression, and β-catenin activity in post-natal growth plate [J].
Chang, Ching-Fang ;
Serra, Rosa .
JOURNAL OF ORTHOPAEDIC RESEARCH, 2013, 31 (03) :350-356