Transcriptome analysis reveals a dynamic and differential transcriptional response to sulforaphane in normal and prostate cancer cells and suggests a role for Sp1 in chemoprevention

被引:27
作者
Beaver, Laura M. [1 ,2 ]
Buchanan, Alex [2 ,3 ]
Sokolowski, Elizabeth I. [2 ]
Riscoe, Allison N. [2 ]
Wong, Carmen P. [1 ,2 ]
Chang, Jeff H. [3 ,4 ]
Loehr, Christiane V. [5 ]
Williams, David E. [1 ,2 ,4 ]
Dashwood, Roderick H. [1 ,2 ,6 ]
Ho, Emily [1 ,2 ,4 ,7 ]
机构
[1] Oregon State Univ, Linus Pauling Inst, Corvallis, OR 97331 USA
[2] Oregon State Univ, Corvallis, OR 97331 USA
[3] Oregon State Univ, Dept Bot & Plant Pathol, Corvallis, OR 97331 USA
[4] Oregon State Univ, Ctr Genome Res & Biocomp, Corvallis, OR 97331 USA
[5] Oregon State Univ, Coll Vet Med, Dept Biomed Sci, Corvallis, OR 97331 USA
[6] Texas A&M Hlth Sci Ctr, Inst Biosci & Technol, Ctr Epigenet & Dis Prevent, Houston, TX USA
[7] Oregon State Univ, Moore Family Ctr, Corvallis, OR 97331 USA
关键词
Chemoprevention; Prostate cancer; RNA sequencing; Specificity protein 1; Sulforaphane; HISTONE DEACETYLASE ACTIVITY; GENE-EXPRESSION PROFILES; ISOTHIOCYANATE SULFORAPHANE; CRUCIFEROUS VEGETABLES; ANDROGEN RECEPTOR; CYCLE ARREST; INHIBITION; 3,3'-DIINDOLYLMETHANE; INDOLE-3-CARBINOL; PROMOTER;
D O I
10.1002/mnfr.201400269
中图分类号
TS2 [食品工业];
学科分类号
0832 ;
摘要
Scope: Epidemiological studies provide evidence that consumption of cruciferous vegetables, like broccoli, can reduce the risk of cancer development. Sulforaphane (SFN) is a phytochemical derived from cruciferous vegetables that induces anti-proliferative and pro-apoptotic responses in prostate cancer cells, but not in normal prostate cells. The mechanisms responsible for this cancer-specific cytotoxicity remain unclear. Methods and results: We utilized RNA sequencing and determined the transcriptomes of normal prostate epithelial cells, androgen-dependent prostate cancer cells, and androgen-independent prostate cancer cells treated with SFN. SFN treatment dynamically altered gene expression and resulted in distinct transcriptome profiles depending on prostate cell line. SFN also down-regulated the expression of genes that were up-regulated in prostate cancer cells. Network analysis of genes altered by SFN treatment revealed that the transcription factor Specificity protein 1 (Sp1) was present in an average of 90.5% of networks. Sp1 protein was significantly decreased by SFN treatment in prostate cancer cells and Sp1 may be an important mediator of SFN-induced changes in expression. Conclusion: Overall, the data show that SFN alters gene expression differentially in normal and cancer cells with key targets in chemopreventive processes, making it a promising dietary anti-cancer agent.
引用
收藏
页码:2001 / 2013
页数:13
相关论文
共 46 条
[1]   Transcriptomic and proteomic profiling of KEAP1 disrupted and sulforaphane-treated human breast epithelial cells reveals common expression profiles [J].
Agyeman, Abena S. ;
Chaerkady, Raghothama ;
Shaw, Patrick G. ;
Davidson, Nancy E. ;
Visvanathan, Kala ;
Pandey, Akhilesh ;
Kensler, Thomas W. .
BREAST CANCER RESEARCH AND TREATMENT, 2012, 132 (01) :175-187
[2]  
American Cancer Society, 2012, Cancer Facts and Figures 2012
[3]  
[Anonymous], GLOBOCAN CANC FACT S
[4]   3,3′-Diindolylmethane, but not indole-3-carbinol, inhibits histone deacetylase activity in prostate cancer cells [J].
Beaver, Laura M. ;
Yu, Tian-Wei ;
Sokolowski, Elizabeth I. ;
Williams, David E. ;
Dashwood, Roderick H. ;
Ho, Emily .
TOXICOLOGY AND APPLIED PHARMACOLOGY, 2012, 263 (03) :345-351
[5]   Predictive Value of Sp1/Sp3/FLIP Signature for Prostate Cancer Recurrence [J].
Bedolla, Roble G. ;
Gong, Jingjing ;
Prihoda, Thomas J. ;
Yeh, I-Tien ;
Thompson, Ian M. ;
Ghosh, Rita ;
Kumar, Addanki P. .
PLOS ONE, 2012, 7 (09)
[6]   Temporal Changes in Gene Expression Induced by Sulforaphane in Human Prostate Cancer Cells [J].
Bhamre, Suvarna ;
Sahoo, Debashis ;
Tibshirani, Robert ;
Dill, David L. ;
Brooks, James D. .
PROSTATE, 2009, 69 (02) :181-190
[7]   Gene Expression Profile of Primary Prostate Epithelial and Stromal Cells in Response to Sulforaphane or Iberin Exposure [J].
Chambers, Karen F. ;
Bacon, James R. ;
Kemsley, E. Katherine ;
Mills, Robert D. ;
Ball, Richard Y. ;
Mithen, Richard F. ;
Traka, Maria H. .
PROSTATE, 2009, 69 (13) :1411-1421
[8]   Sulforaphane Induction of p21Cip1 Cyclin-dependent Kinase Inhibitor Expression Requires p53 and Sp1 Transcription Factors and Is p53-dependent [J].
Chew, Yap Ching ;
Adhikary, Gautam ;
Wilson, Gerald M. ;
Xu, Wen ;
Eckert, Richard L. .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2012, 287 (20) :16168-16178
[9]   Betulinic acid inhibits prostate cancer growth through inhibition of specificity protein transcription factors [J].
Chintharlapalli, Sudhakar ;
Papineni, Sabitha ;
Ramaiah, Shashi K. ;
Safe, Stephen .
CANCER RESEARCH, 2007, 67 (06) :2816-2823
[10]   Metabolism and Tissue Distribution of Sulforaphane in Nrf2 Knockout and Wild-Type Mice [J].
Clarke, John D. ;
Hsu, Anna ;
Williams, David E. ;
Dashwood, Roderick H. ;
Stevens, Jan F. ;
Yamamoto, Masayuki ;
Ho, Emily .
PHARMACEUTICAL RESEARCH, 2011, 28 (12) :3171-3179