Spindle pole body component 25 regulates stemness of prostate cancer cells

被引:28
作者
Cui, Feilun [1 ]
Tang, Huaming [1 ]
Tan, Jian [1 ]
Hu, Jianpeng [1 ]
机构
[1] Zhenjiang First Peoples Hosp, Dept Urol, Zhenjiang 212002, Peoples R China
来源
AGING-US | 2018年 / 10卷 / 11期
关键词
cancer stem cells (CSCs); SPC25; prostate cancer (PrC); NEXT-GENERATION; CD133;
D O I
10.18632/aging.101631
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Spindle pole body component 25 (SPC25) is a component of NDC80 complex that controls spindle assembly checkpoint in the microtubule-binding domain of kinetochores. We recently showed that SPC25 is required for prostate cancer (PrC) cell proliferation and cell cycle progression, and here we investigated whether SPC25 may be a Cancer stem cell (CSC) marker in PrC. We found that the levels of SPC25 were higher in PrC samples than paired normal prostate tissue. The overall survival of PrC patients with high SPC25 was poorer than those with low SPC25. PrC cell lines were transduced with two vectors carrying a luciferase reporter and a mCherry fluorescent reporter under a cytomegalovirus promoter and a nuclear green fluorescent protein reporter under the control of a SPC25 promoter, respectively, to allow differentiating SPC25+ from SPC25- PrC cells by flow cytometry. Compared to SPC25- cells, SPC25+ cells formed significantly more tumor spheres in culture, appeared to be more resistant towards docetaxel-induced cell apoptosis, and generated larger tumors with higher frequency after serial adoptive transplantation. Thus, our data suggest that SPC25 may be highly expressed in the CSC-like cells in PrC and could be a promising target for effective treatment of PrC.
引用
收藏
页码:3273 / 3282
页数:10
相关论文
共 20 条
[1]   Insights into the next generation of cancer stem cell research [J].
Brown, Daniel V. ;
Mantamadiotis, Theo .
FRONTIERS IN BIOSCIENCE-LANDMARK, 2014, 19 :1015-1027
[2]   SPC25 upregulation increases cancer stem cell properties in non-small cell lung adenocarcinoma cells and independently predicts poor survival [J].
Chen, Jingxia ;
Chen, Hongfen ;
Yang, Hanbing ;
Dai, Huizhen .
BIOMEDICINE & PHARMACOTHERAPY, 2018, 100 :233-239
[3]   Knockdown of spindle pole body component 25 homolog inhibits cell proliferation and cycle progression in prostate cancer [J].
Cui, Feilun ;
Hu, Jianpeng ;
Fan, Yu ;
Tan, Jian ;
Tang, Huaming .
ONCOLOGY LETTERS, 2018, 15 (04) :5712-5720
[4]   The glycosyltransferase ST6Gal-I is enriched in cancer stem-like cells in colorectal carcinoma and contributes to their chemo-resistance [J].
Cui, H. ;
Yang, S. ;
Jiang, Y. ;
Li, C. ;
Zhao, Y. ;
Shi, Y. ;
Hao, Y. ;
Qian, F. ;
Tang, B. ;
Yu, P. .
CLINICAL & TRANSLATIONAL ONCOLOGY, 2018, 20 (09) :1175-1184
[5]   Recent Advances in Understanding Hormonal Therapy Resistant Prostate Cancer [J].
Donkena, K. V. ;
Yuan, H. ;
Young, C. Y. .
CURRENT CANCER DRUG TARGETS, 2010, 10 (04) :402-410
[6]  
Fonseka Laksha N, 2015, J Assoc Genet Technol, V41, P100
[7]   The Role of CD133 in Normal Human Prostate Stem Cells and Malignant Cancer-Initiating Cells [J].
Griend, Donald J. Vander ;
Karthaus, Wouter L. ;
Dalrymple, Susan ;
Meeker, Alan ;
DeMarzo, Angelo M. ;
Isaacs, John T. .
CANCER RESEARCH, 2008, 68 (23) :9703-9711
[8]   Spindle pole body component 25 homolog expressed by ECM stiffening is required for lung cancer cell proliferation [J].
Jeong, Jangho ;
Keum, Seula ;
Kim, Daehwan ;
You, Eunae ;
Ko, Panseon ;
Lee, Jieun ;
Kim, Jaegu ;
Kim, Jung-Woong ;
Rhee, Sangmyung .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2018, 500 (04) :937-943
[9]  
Kruslin B, 2015, BOSNIAN J BASIC MED, V15, P1, DOI 10.17305/bjbms.2015.449
[10]   Investigating core genetic-and-epigenetic cell cycle networks for stemness and carcinogenic mechanisms, and cancer drug design using big database mining and genome-wide next-generation sequencing data [J].
Li, Cheng-Wei ;
Chen, Bor-Sen .
CELL CYCLE, 2016, 15 (19) :2593-2607