The role of the histone H3 variant CENPA in prostate cancer

被引:54
作者
Saha, Anjan K. [1 ,2 ,3 ]
Contreras-Galindo, Rafael [3 ]
Niknafs, Yashar S. [1 ,7 ,8 ]
Iyer, Matthew [4 ,8 ]
Qin, Tingting [4 ]
Padmanabhan, Karthik [4 ]
Siddiqui, Javed [5 ,8 ]
Palande, Monica [3 ]
Wang, Claire [3 ]
Qian, Brian [3 ]
Ward, Elizabeth [3 ]
Tang, Tara [3 ]
Tomlins, Scott A. [5 ,8 ]
Gitlin, Scott D. [3 ]
Sartor, Maureen A. [4 ]
Omenn, Gilbert S. [3 ,4 ,6 ]
Chinnaiyan, Arul M. [2 ,4 ,5 ,7 ,8 ,10 ]
Markovitz, David M. [2 ,3 ,7 ,9 ]
机构
[1] Univ Michigan, Med Scientist Training Program, Ann Arbor, MI 48109 USA
[2] Univ Michigan, Program Canc Biol, Ann Arbor, MI 48109 USA
[3] Univ Michigan, Dept Internal Med, Ann Arbor, MI 48109 USA
[4] Univ Michigan, Dept Computat Med & Bioinformat, Ann Arbor, MI 48109 USA
[5] Univ Michigan, Dept Pathol, Ann Arbor, MI 48109 USA
[6] Univ Michigan, Dept Human Genet, Ann Arbor, MI 48109 USA
[7] Univ Michigan, Program Cellular & Mol Biol, Ann Arbor, MI 48109 USA
[8] Univ Michigan, Michigan Ctr Translat Pathol, Ann Arbor, MI 48109 USA
[9] Univ Michigan, Program Immunol, Ann Arbor, MI 48109 USA
[10] Univ Michigan, Howard Hughes Med Inst, Ann Arbor, MI 48109 USA
基金
美国国家卫生研究院;
关键词
Centromere; prostate cancer; epigenetics; histone; gene expression; centromere protein A (CENPA); gene regulation; transcription; chromatin; cell proliferation; centromere; CENTROMERE PROTEIN-A; INTEGRATIVE CLINICAL GENOMICS; PROGNOSTIC VALUE; EXPRESSION; NUCLEOSOMES; GENE; CHROMATIN; MARKER; KI-67; HJURP;
D O I
10.1074/jbc.RA119.010080
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
Overexpression of centromeric proteins has been identified in a number of human malignancies, but the functional and mechanistic contributions of these proteins to disease progression have not been characterized. The centromeric histone H3 variant centromere protein A (CENPA) is an epigenetic mark that determines centromere identity. Here, using an array of approaches, including RNA-sequencing and ChIP-sequencing analyses, immunohistochemistry-based tissue microarrays, and various cell biology assays, we demonstrate that CENPA is highly overexpressed in prostate cancer in both tissue and cell lines and that the level of CENPA expression correlates with the disease stage in a large cohort of patients. Gain-of-function and loss-of-function experiments confirmed that CENPA promotes prostate cancer cell line growth. The results from the integrated sequencing experiments suggested a previously unidentified function of CENPA as a transcriptional regulator that modulates expression of critical proliferation, cell-cycle, and centromere/kinetochore genes. Taken together, our findings show that CENPA overexpression is crucial to prostate cancer growth.
引用
收藏
页码:8537 / 8549
页数:13
相关论文
共 50 条
[1]  
[Anonymous], 2018, American Cancer Society: Cancer Facts and Figures 2018
[2]   CENP-A nucleosomes localize to transcription factor hotspots and subtelomeric sites in human cancer cells [J].
Athwal, Rajbir K. ;
Walkiewicz, Marcin P. ;
Baek, Songjoon ;
Fu, Song ;
Bui, Minh ;
Camps, Jordi ;
Ried, Thomas ;
Sung, Myong-Hee ;
Dalal, Yamini .
EPIGENETICS & CHROMATIN, 2015, 8
[3]   HJURP is a CENP-A chromatin assembly factor sufficient to form a functional de novo kinetochore [J].
Barnhart, Meghan C. ;
Kuich, P. Henning J. L. ;
Stellfox, Madison E. ;
Ward, Jared A. ;
Bassett, Emily A. ;
Black, Ben E. ;
Foltz, Daniel R. .
JOURNAL OF CELL BIOLOGY, 2011, 194 (02) :229-243
[4]   Centromere identity maintained by nucleosomes assembled with histone H3 containing the CENP-A targeting domain [J].
Black, Ben E. ;
Jansen, Lars E. T. ;
Maddox, Paul S. ;
Foltz, Daniel R. ;
Desai, Arshad B. ;
Shah, Jagesh V. ;
Cleveland, Don W. .
MOLECULAR CELL, 2007, 25 (02) :309-322
[5]   The quantitative architecture of centromeric chromatin [J].
Bodor, Dani L. ;
Mata, Joao F. ;
Sergeev, Mikhail ;
David, Ana Filipa ;
Salimian, Kevan J. ;
Panchenko, Tanya ;
Cleveland, Don W. ;
Black, Ben E. ;
Shah, Jagesh V. ;
Jansen, Lars E. T. .
ELIFE, 2014, 3
[6]   Androgens Suppress EZH2 Expression Via Retinoblastoma (RB) and p130-Dependent Pathways: A Potential Mechanism of Androgen-Refractory Progression of Prostate Cancer [J].
Bohrer, Laura R. ;
Chen, Shuai ;
Hallstrom, Timothy C. ;
Huang, Haojie .
ENDOCRINOLOGY, 2010, 151 (11) :5136-5145
[7]   An ultra-low-input native ChIP-seq protocol for genome-wide profiling of rare cell populations [J].
Brind'Amour, Julie ;
Liu, Sheng ;
Hudson, Matthew ;
Chen, Carol ;
Karimi, Mohammad M. ;
Lorincz, Matthew C. .
NATURE COMMUNICATIONS, 2015, 6
[8]   Centromeres and kinetochores: From epigenetics to mitotic checkpoint signaling [J].
Cleveland, DW ;
Mao, YH ;
Sullivan, KF .
CELL, 2003, 112 (04) :407-421
[9]   Rapid molecular assays to study human centromere genomics [J].
Contreras-Galindo, Rafael ;
Fischer, Sabrina ;
Saha, Anjan K. ;
Lundy, John D. ;
Cervantes, Patrick W. ;
Mourad, Mohamad ;
Wang, Claire ;
Qian, Brian ;
Dai, Manhong ;
Meng, Fan ;
Chinnaiyan, Arul ;
Omenn, Gilbert S. ;
Kaplan, Mark H. ;
Markovitz, David M. .
GENOME RESEARCH, 2017, 27 (12) :2040-2049
[10]   A new look at prostate cancer treatment complications [J].
Cooperberg, Matthew R. .
NATURE REVIEWS CLINICAL ONCOLOGY, 2014, 11 (06) :304-305