Epigenetics: an emerging technology in the diagnosis and treatment of cancer

被引:28
作者
Stebbing, Justin
Bower, Mark
Syed, Nelofer
Smith, Paul
Yu, Veronica
Crook, Tim [1 ]
机构
[1] Inst Canc Res, Canc Genet & Epigenet Lab, Toby Robins Breakthrough Breast Canc Ctr, London SW3 6JB, England
[2] St Bartholomews Hosp, Dept Med Oncol, London, England
[3] Chelsea & Westminster Hosp, Dept Med Oncol, London SW10, England
[4] Univ London Imperial Coll Sci Technol & Med, MRC, Ctr Clin Sci, Eukaryot Chromatin Dynam Grp, London W12 0NN, England
[5] Charing Cross Hosp, Dept Med Oncol, London W6 8RF, England
基金
英国医学研究理事会;
关键词
epigenetics; methylation; tumor suppressor gene;
D O I
10.2217/14622416.7.5.747
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Transcriptional silencing resulting from changes in epigenetic regulation of gene expression is the most frequent mechanism by which tumor suppressor genes are inactivated in human cancer. Genes participating in numerous functional groups and pathways leading to malignancy are subject to aberrant CpG methylation, with associated downregulation of expression, in human carcinogenesis. Methylation profiling can identify distinct subtypes of common human cancers and may have utility in predicting clinical phenotypes in individual patients, including sensitivity to chemotherapeutic agents. Hypomethylating agents have clinical activity in some hematological malignancies, and there is accumulating evidence correlating clinical response with demethylation and concomitant reactivation of expression of specific target genes. Epigenetic analysis is likely to have an increasingly important part to play in the diagnosis, prognostic assessment and treatment of malignant disease.
引用
收藏
页码:747 / 757
页数:11
相关论文
共 53 条
[1]   Promoter hypermethylation of p15INK4B, HIC1, CDH1, and ER is frequent in myelodysplastic syndrome and predicts poor prognosis in early-stage patients [J].
Aggerholm, A ;
Holm, MS ;
Guldberg, P ;
Olesen, LH ;
Hokland, P .
EUROPEAN JOURNAL OF HAEMATOLOGY, 2006, 76 (01) :23-32
[2]   ASPP1, a common activator of TP53, is inactivated by aberrant methylation of its promoter in acute lymphoblastic leukemia [J].
Agirre, X ;
Román-Gómez, J ;
Jiménez-Velasco, A ;
Garate, L ;
Montiel-Duarte, C ;
Navarro, G ;
Vázquez, I ;
Zalacain, M ;
Calasanz, MJ ;
Heiniger, A ;
Torres, A ;
Minna, JD ;
Prósper, F .
ONCOGENE, 2006, 25 (13) :1862-1870
[3]   Antimitogenic and chernosensitizing effects of the methylation inhibitor zebularine in ovarian cancer [J].
Balch, C ;
Yan, P ;
Craft, T ;
Young, S ;
Skalnik, DG ;
Huang, THM ;
Nephew, KP .
MOLECULAR CANCER THERAPEUTICS, 2005, 4 (10) :1505-1514
[4]   Methyl-CpG binding proteins identify novel sites of epigenetic inactivation in human cancer [J].
Ballestar, E ;
Paz, MF ;
Valle, L ;
Wei, S ;
Fraga, MF ;
Espada, J ;
Cigudosa, JC ;
Huang, THM ;
Esteller, M .
EMBO JOURNAL, 2003, 22 (23) :6335-6345
[5]   DNA methylation and gene silencing in cancer [J].
Baylin S.B. .
Nature Clinical Practice Oncology, 2005, 2 (Suppl 1) :S4-S11
[6]   p53 polymorphism influences response in cancer chemotherapy via modulation of p73-dependent apoptosis [J].
Bergamaschi, D ;
Gasco, M ;
Hiller, L ;
Sullivan, A ;
Syed, N ;
Trigiante, G ;
Yulug, I ;
Merlano, M ;
Numico, G ;
Comino, A ;
Attard, M ;
Reelfs, O ;
Gusterson, B ;
Bell, AK ;
Heath, V ;
Tavassoli, M ;
Farrell, PJ ;
Smith, P ;
Lu, X ;
Crook, T .
CANCER CELL, 2003, 3 (04) :387-402
[7]   MUTATOR PHENOTYPES IN HUMAN COLORECTAL-CARCINOMA CELL-LINES [J].
BHATTACHARYYA, NP ;
SKANDALIS, A ;
GANESH, A ;
GRODEN, J ;
MEUTH, M .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1994, 91 (14) :6319-6323
[8]   Silencing of the novel p53 target gene Snk/Plk2 leads to mitotic catastrophe in paclitaxel (Taxol)-exposed cells [J].
Burns, TF ;
Fei, PW ;
Scata, KA ;
Dicker, DT ;
El-Deiry, WS .
MOLECULAR AND CELLULAR BIOLOGY, 2003, 23 (16) :5556-5571
[9]   Tamoxifen-resistant breast cancers show less frequent methylation of the estrogen receptor β but not the estrogen receptor αgene [J].
Chang, HG ;
Kim, SJ ;
Chung, KW ;
Noh, DY ;
Kwon, Y ;
Lee, ES ;
Kang, HS .
JOURNAL OF MOLECULAR MEDICINE-JMM, 2005, 83 (02) :132-139
[10]  
CHRISTMAN JK, 1983, CANCER RES, V43, P763