Nucleic acid quantification and disease outcome prediction in colorectal cancer

被引:5
作者
Bustin, Stephen A.
机构
[1] Royal London Hosp, Ctr Acad Surg, London E1 1BB, England
[2] Univ London, Inst Cell & Mol Sci, Barts & London Queen Marys Sch Med & Dent, London, England
关键词
cancer; colon; metastasis; microarray; occult disease; polymerase chain reaction; reverse transcription; staging;
D O I
10.2217/17410541.3.2.207
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Histopathological stage at diagnosis remains the most important prognostic determinant for colorectal cancer. However, conventional staging is unable to predict disease outcome accurately for each individual patient. This results in considerable prognostic heterogeneity within a given tumor stage and is of particular relevance for a subgroup of patients with stage II disease that would benefit from adjuvant therapy. The recent advances in functional genomics are beginning to have a significant impact on clinical oncology, and there is widespread interest in using molecular techniques for clinical applications. These have focused on two approaches: the use of polymerase chain reaction (PCR)-based methods for the detection of occult disease in lymph nodes, bone marrow and blood and the use of microarrays for the expression profiling of primary tumors. The aim is to develop molecular classifiers that will allow the prediction of disease outcome, thus matching patients with individualized treatment. Despite the obvious attractions of these approaches, there have been significant technical, biological and analytical problems in their translation into clinically relevant practice. This is particularly true for colorectal cancer, the second most common cancer in the western world. Nevertheless, progress is being made and the improved awareness and appreciation of those difficulties is beginning to generate results that should prove useful for clinical oncology.
引用
收藏
页码:207 / 216
页数:10
相关论文
共 79 条
[1]   Comparative evaluation of measles virus-specific RT-PCR methods through an international collaborative study [J].
Afzal, MA ;
Osterhaus, ADME ;
Cosby, SL ;
Jin, L ;
Beeler, J ;
Takeuchi, K ;
Kawashima, H .
JOURNAL OF MEDICAL VIROLOGY, 2003, 70 (01) :171-176
[2]   Artificial neural networks for diagnosis and survival prediction in colon cancer [J].
Ahmed, Farid E. .
MOLECULAR CANCER, 2005, 4 (1)
[3]   Molecular markers that predict response to colon cancer therapy [J].
Ahmed, FE .
EXPERT REVIEW OF MOLECULAR DIAGNOSTICS, 2005, 5 (03) :353-375
[4]   Development of novel diagnostic and prognostic molecular markers for sporadic colon cancer [J].
Ahmed, FE .
EXPERT REVIEW OF MOLECULAR DIAGNOSTICS, 2005, 5 (03) :337-352
[5]  
Al-Mulla F, 1999, GENE CHROMOSOME CANC, V24, P306, DOI 10.1002/(SICI)1098-2264(199904)24:4<306::AID-GCC3>3.0.CO
[6]  
2-5
[7]   Broad patterns of gene expression revealed by clustering analysis of tumor and normal colon tissues probed by oligonucleotide arrays [J].
Alon, U ;
Barkai, N ;
Notterman, DA ;
Gish, K ;
Ybarra, S ;
Mack, D ;
Levine, AJ .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1999, 96 (12) :6745-6750
[8]   K-ras mutations are found in DNA extracted from the plasma of patients with colorectal cancer [J].
Anker, P ;
Lefort, F ;
Vasioukhin, V ;
Lyautey, J ;
Lederrey, C ;
Chen, XQ ;
Stroun, M ;
Mulcahy, HE ;
Farthing, MJG .
GASTROENTEROLOGY, 1997, 112 (04) :1114-1120
[9]   Gene-expression profiling predicts recurrence in Dukes' C colorectal cancer [J].
Arango, D ;
Laiho, P ;
Kokko, A ;
Alhopuro, P ;
Sammalkorpi, H ;
Salovaara, R ;
Nicorici, D ;
Hautaniemi, S ;
Alazzouzi, H ;
Salovaara, R ;
Nicorici, D ;
Hautaniemi, S ;
Alazzouzi, H ;
Mecklin, JP ;
Järvinen, H ;
Hemminki, A ;
Astola, J ;
Schwartz, S ;
Aaltonen, LA .
GASTROENTEROLOGY, 2005, 129 (03) :874-884
[10]   Intratumor genetic heterogeneity in advanced human colorectal adenocarcinoma [J].
Baisse, B ;
Bouzourene, H ;
Saraga, EP ;
Bosman, FT ;
Benhattar, J .
INTERNATIONAL JOURNAL OF CANCER, 2001, 93 (03) :346-352