Circulating Nucleic Acids as a Potential Source for Cancer Biomarkers

被引:89
作者
Vlassov, V. V. [1 ]
Laktionov, P. P. [1 ]
Rykova, E. Y. [1 ]
机构
[1] SD RAS, Inst Chem Biol & Fundamental Med, Novosibirsk 630090, Russia
基金
俄罗斯基础研究基金会;
关键词
Circulating DNA; RNA; cancer; diagnostics; genetic mutations; allelic imbalance; gene methylation; microRNA; BARR-VIRUS DNA; CELL-FREE DNA; HUMAN-PAPILLOMAVIRUS DNA; TIME QUANTITATIVE PCR; ABERRANT PROMOTER METHYLATION; TRANSCRIPTASE MESSENGER-RNA; BONE-MARROW PLASMA; TUMOR-SPECIFIC DNA; K-RAS MUTATIONS; LUNG-CANCER;
D O I
10.2174/156652410790963295
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Since the association of circulating DNA level changes with tumor growth was discovered many attempts have been made to develop the sensitive and robust blood-based tests for early tumor diagnostics. Both genomic as well as mitochondrial DNA quantification in the circulation have been extensively evaluated as a diagnostic and prognostic tool to monitor cancer therapy. Cell-free DNA bearing the same genetic and epigenetic changes as the tumor tissues were shown to be detectable in plasma / serum of cancer patients indicating the principal possibility to create the minimally invasive diagnostic tests based on tumor-specific DNA markers. Apart from circulating DNA, tumor-derived RNA in plasma / serum was found to be a promising approach for the development of cancer markers. Results of the last two years establish the quantification of the tumor-derived microRNAs in plasma / serum as an extremely promising approach for cancer diagnostics. The aim of this publication was to review the recently reported studies on the circulating DNA and RNA in cancer patients and to estimate their impact on making the ongoing research closer to clinical application.
引用
收藏
页码:142 / 165
页数:24
相关论文
共 237 条
[91]   Early p53 mutations in nondysplastic Barrett's tissue detected by the restriction site mutation (RSM) methodology [J].
Jenkins, GJS ;
Doak, SH ;
Griffiths, AP ;
Tofazzal, N ;
Shah, V ;
Baxter, JN ;
Parry, JM .
BRITISH JOURNAL OF CANCER, 2003, 88 (08) :1271-1276
[92]   Mitochondrial mutations in early stage prostate cancer and bodily fluids [J].
Jerónimo, C ;
Nomoto, S ;
Caballero, OL ;
Usadel, H ;
Henrique, R ;
Varzim, G ;
Oliveira, J ;
Lopes, C ;
Fliss, MS ;
Sidransky, D .
ONCOGENE, 2001, 20 (37) :5195-5198
[93]   Increased plasma DNA integrity index in head and neck cancer patients [J].
Jiang, Wei-Wen ;
Zahurak, Marianna ;
Goldenberg, David ;
Milman, Yelena ;
Park, Hannah Lui ;
Westra, William H. ;
Koch, Wayne ;
Sidransky, David ;
Califano, Joseph .
INTERNATIONAL JOURNAL OF CANCER, 2006, 119 (11) :2673-2676
[94]   Increased mitochondrial DNA content in saliva associated with head and neck cancer [J].
Jiang, WW ;
Masayesva, B ;
Zahurak, M ;
Carvalho, AL ;
Rosenbaum, E ;
Mambo, E ;
Zhou, SY ;
Minhas, K ;
Benoit, N ;
Westra, WH ;
Alberg, A ;
Sidransky, D ;
Koch, W ;
Califano, J .
CLINICAL CANCER RESEARCH, 2005, 11 (07) :2486-2491
[95]  
Johnson PJ, 2002, CLIN CHEM, V48, P1186
[96]   Increased cell-free DNA in plasma of patients with metastatic spread in prostate cancer [J].
Jung, K ;
Stephan, C ;
Lewandowski, M ;
Klotzek, S ;
Jung, M ;
Kristiansen, G ;
Lein, M ;
Loening, SA ;
Schnorr, D .
CANCER LETTERS, 2004, 205 (02) :173-180
[97]  
Kagan Jacob, 2007, Cancer Res, V67, P4545, DOI 10.1158/0008-5472.CAN-06-2888
[98]   Microsatellite analysis of serum DNA in patients with oral squamous cell carcinoma [J].
Kakimoto, Yoshidou ;
Yamamoto, Nobuharu ;
Shibahara, Takahiko .
ONCOLOGY REPORTS, 2008, 20 (05) :1195-1200
[99]   Quantification of total plasma cell-free DNA in ovarian cancer using real-time PCR [J].
Kamat, Aparna A. ;
Sood, Anil K. ;
Dang, Dianne ;
Gershenson, David M. ;
Simpson, Joe L. ;
Bischoff, Farideh Z. .
CIRCULATING NUCLEIC ACIDS IN PLASMA AND SERUM IV, 2006, 1075 :230-234
[100]   Epithelial molecular markers in the peripheral blood of patients with colorectal cancer [J].
Khair, Ghaith ;
Monson, John R. T. ;
Greenman, John .
DISEASES OF THE COLON & RECTUM, 2007, 50 (08) :1188-1203