Prognostic DNA methylation marker in serum of cancer patients

被引:67
作者
Müller, HM
Fiegl, H
Widschwendter, A
Widschwendter, M
机构
[1] Innsbruck Med Univ, Dept Obstet & Gynecol, A-6020 Innsbruck, Austria
[2] Innsbruck Med Univ, Dept Gen & Transplant Surg, A-6020 Innsbruck, Austria
来源
CIRCULATING NUCLEIC ACIDS IN PLASMA/SERUM III AND SERUM PROTEOMICS | 2004年 / 1022卷
关键词
DNA methylation; cervical cancer; breast cancer; prognosis; serum;
D O I
10.1196/annals.1318.008
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
Changes in the status of DNA methylation are among the most common molecular alterations in human neoplasia. Recent demonstrations of tumor-derived methylated DNA in the blood stream of cancer patients allow the use of these epigenetic markers for risk assessment in cancer patients. We were interested in evaluating the prognostic value of several methylated genes in the serum of cancer patients. Using MethyLight, a high-throughput DNA methylation assay, we analyzed 215 serum samples from patients with cervical (n = 93) or breast cancer (n = 122) for DNA methylation changes. In cervical cancer, hypermethylation of three genes (MYOD1, CDH1, and CDH13) in pretreatment sera was statistically significantly associated with a poorer disease outcome. Additionally, for the first time we used a so-called gene evaluation set to identify the most important DNA methylation changes in the serum of breast cancer patients from a long list of candidate genes. In the gene evaluation set, we detected five genes (ESR1, APC, HSD17B4, HIC1, and RASSF1A) using our criteria for further analysis. Finally, two of the evaluated genes (APC and RASSF1A) proved to be independent prognostic parameters in breast cancer patients. In summary, we detected several prognostic DNA methylation markers in the serum of cervical and breast cancer patients. This finding indicates great potential for the use of these epigenetic markers in clinical, routine risk assessment in patients with various malignancies.
引用
收藏
页码:44 / 49
页数:6
相关论文
共 15 条
[1]   Detection of circulating tumour DNA in the blood (plasma/serum) of cancer patients [J].
Anker, P ;
Mulcahy, H ;
Chen, XQ ;
Stroun, M .
CANCER AND METASTASIS REVIEWS, 1999, 18 (01) :65-73
[2]  
Eads CA, 2001, CANCER RES, V61, P3410
[3]   MethyLight: a high-throughput assay to measure DNA methylation [J].
Eads, Cindy A. ;
Danenberg, Kathleen D. ;
Kawakami, Kazuyuki ;
Saltz, Leonard B. ;
Blake, Corey ;
Shibata, Darryl ;
Danenberg, Peter V. ;
Laird, Peter W. .
NUCLEIC ACIDS RESEARCH, 2000, 28 (08) :32
[4]  
García-Olmo D, 2001, ANN NY ACAD SCI, V945, P265
[5]   Hypermethylation at 9q32-33 tumour suppressor region is age-related in normal urothelium and an early and frequent alteration in bladder cancer [J].
Habuchi, T ;
Takahashi, T ;
Kakinuma, H ;
Wang, LZ ;
Tsuchiya, N ;
Satoh, S ;
Akao, T ;
Sato, K ;
Ogawa, O ;
Knowles, MA ;
Kato, T .
ONCOGENE, 2001, 20 (04) :531-537
[6]  
Issa JPJ, 2001, CANCER RES, V61, P3573
[7]   The fundamental role of epigenetic events in cancer [J].
Jones, PA ;
Baylin, SB .
NATURE REVIEWS GENETICS, 2002, 3 (06) :415-428
[8]   Genetic heterogeneity of single disseminated tumour cells in minimal residual cancer [J].
Klein, CA ;
Blankenstein, TJF ;
Schmidt-Kittler, O ;
Petronio, M ;
Polzer, B ;
Stoecklein, NH ;
Riethmüller, G .
LANCET, 2002, 360 (9334) :683-689
[9]   The power and the promise of DNA methylation markers [J].
Laird, PW .
NATURE REVIEWS CANCER, 2003, 3 (04) :253-266
[10]  
LEON SA, 1977, CANCER RES, V37, P646