Epigenetic Changes During Cell Transformation

被引:23
作者
Futscher, Bernard W. [1 ,2 ]
机构
[1] Univ Arizona, Coll Pharm, Dept Pharmacol & Toxicol, Tucson, AZ 85724 USA
[2] Univ Arizona, Univ Arizona Canc Ctr, Tucson, AZ 85724 USA
来源
EPIGENETIC ALTERATIONS IN ONCOGENESIS | 2013年 / 754卷
关键词
MAMMARY EPITHELIAL-CELLS; INDUCED MALIGNANT-TRANSFORMATION; DNA METHYLATION; ARSENIC NEUROTOXICITY; HUMAN KERATINOCYTES; GROWTH-INHIBITION; CANCER; BLADDER; INACTIVATION; SENESCENCE;
D O I
10.1007/978-1-4419-9967-2_9
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Malignant cancer emerges from normal healthy cells in a multistep process that involves both genetic and epigenetic lesions. Both genetic and environmental inputs participate in driving the epigenetic changes that occur during human carcinogenesis. The pathologic changes seen in DNA methylation and histone posttranslational modifications are complex, deeply intertwined, and act in concert to produce malignant transformation. To better understand the causes and consequences of the pathoepigenetic changes in cancer formation, a variety of experimentally tractable human cell line model systems that accurately reflect the molecular alterations seen in the clinical disease have been developed. Results from studies using these cell line model systems suggest that early critical epigenetic events occur in a stepwise fashion prior to cell immortalization. These epigenetic steps coincide with the cell's transition through well-defined cell proliferation barriers of stasis and telomere dysfunction. Following cell immortalization, stressors, such as environmental toxicants, can induce malignant transformation in a process in which the epigenetic changes occur in a smoother progressive fashion, in contrast to the stark stepwise epigenetic changes seen prior to cell immortalization. It is hoped that developing a clearer understanding of the identity, timing, and consequences of these epigenetic lesions will prove useful in future clinical applications that range from early disease detection to therapeutic intervention in malignant cancer.
引用
收藏
页码:179 / 194
页数:16
相关论文
共 65 条
[1]   Inorganic arsenite-induced malignant transformation of human prostate epithelial cells [J].
Achanzar, WE ;
Brambila, EM ;
Diwan, BA ;
Webber, MM ;
Waalkes, MP .
JNCI-JOURNAL OF THE NATIONAL CANCER INSTITUTE, 2002, 94 (24) :1888-1891
[2]   NEOPLASTIC TRANSFORMATION OF A HUMAN BRONCHIAL EPITHELIAL-CELL LINE BY A RECOMBINANT RETROVIRUS ENCODING VIRAL HARVEY RAS [J].
AMSTAD, P ;
REDDEL, RR ;
PFEIFER, A ;
MALANSHIBLEY, L ;
MARK, GE ;
HARRIS, CC .
MOLECULAR CARCINOGENESIS, 1988, 1 (03) :151-160
[3]   Androgen responsive adult human prostatic epithelial cell lines immortalized by human papillomavirus 18 [J].
Bello, D ;
Webber, MM ;
Kleinman, HK ;
Wartinger, DD ;
Rhim, JS .
CARCINOGENESIS, 1997, 18 (06) :1215-1223
[4]   Molecular events associated with arsenic-induced malignant transformation of human prostatic epithelial cells: aberrant genomic DNA methylation and K-ras oncogene activation [J].
Benbrahim-Tallaa, L ;
Waterland, RA ;
Styblo, M ;
Achanzar, WE ;
Webber, MM ;
Waalkes, MP .
TOXICOLOGY AND APPLIED PHARMACOLOGY, 2005, 206 (03) :288-298
[5]   NORMAL KERATINIZATION IN A SPONTANEOUSLY IMMORTALIZED ANEUPLOID HUMAN KERATINOCYTE CELL-LINE [J].
BOUKAMP, P ;
PETRUSSEVSKA, RT ;
BREITKREUTZ, D ;
HORNUNG, J ;
MARKHAM, A ;
FUSENIG, NE .
JOURNAL OF CELL BIOLOGY, 1988, 106 (03) :761-771
[6]   Monomethylarsonous acid induces transformation of human bladder cells [J].
Bredfeldt, Tiffany G. ;
Jagadish, Bhumasamudram ;
Eblin, Kylee E. ;
Mash, Eugene A. ;
Gandolfi, A. Jay .
TOXICOLOGY AND APPLIED PHARMACOLOGY, 2006, 216 (01) :69-79
[7]   Increased p16 expression with first senescence arrest in human mammary epithelial cells and extended growth capacity with p16 inactivation [J].
Brenner, AJ ;
Stampfer, MR ;
Aldaz, CM .
ONCOGENE, 1998, 17 (02) :199-205
[8]   p53 regulates epithelial-mesenchymal transition and stem cell properties through modulating miRNAs [J].
Chang, Chun-Ju ;
Chao, Chi-Hong ;
Xia, Weiya ;
Yang, Jer-Yen ;
Xiong, Yan ;
Li, Chia-Wei ;
Yu, Wen-Hsuan ;
Rehman, Sumaiyah K. ;
Hsu, Jennifer L. ;
Lee, Heng-Huan ;
Liu, Mo ;
Chen, Chun-Te ;
Yu, Dihua ;
Hung, Mien-Chie .
NATURE CELL BIOLOGY, 2011, 13 (03) :317-U296
[9]   Reduced Reactive Oxygen Species-Generating Capacity Contributes to the Enhanced Cell Growth of Arsenic-Transformed Epithelial Cells [J].
Chang, Qingshan ;
Pan, Jingju ;
Wang, Xing ;
Zhang, Zhuo ;
Chen, Fei ;
Shi, Xianglin .
CANCER RESEARCH, 2010, 70 (12) :5127-5135
[10]   Expression of hTERT immortalises normal human urothelial cells without inactivation of the p16/Rb pathway [J].
Chapman, E. J. ;
Hurst, C. D. ;
Pitt, E. ;
Chambers, P. ;
Aveyard, J. S. ;
Knowles, M. A. .
ONCOGENE, 2006, 25 (36) :5037-5045