Gene expression profile in breast cancer comprising predictive markers for metastatic risk

被引:3
|
作者
Sirirattanakul, S. [1 ]
Wannakrairot, P. [2 ]
Tencomnao, T. [3 ]
Santiyanont, R. [3 ]
机构
[1] Chulalongkorn Univ, Fac Allied Hlth Sci, Dept Clin Chem, Grad Program Clin Biochem & Mol Med, Bangkok, Thailand
[2] Chulalongkorn Univ, Fac Med, Dept Pathol, Bangkok 10330, Thailand
[3] Chulalongkorn Univ, Fac Allied Hlth Sci, Dept Clin Chem, Bangkok, Thailand
关键词
Multiplex RT-PCR; Breast cancer; Metastasis; GIT2; MTERF; GEXP ANALYZER; PROTEINS; PCR; ADHESION; DESIGN; FAMILY; COLON; ASSAY; GIT2;
D O I
10.4238/2015.September.21.3
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
Quantitative multiplex reverse transcriptase-polymerase chain reaction was developed for the simultaneous detection of multiple-gene expression levels of formalin-fixed, paraffin-embedded breast cancer samples. Candidate genes were selected from previous microarray data relevant to breast cancer markers that had the potential to serve as predictive markers for metastatic risk. This multiplex gene set included 11 candidate and 3 housekeeping genes, and the aim was to predict breast cancer progression based on lymph node involvement status. Our study demonstrated that the system generated a good standard curve fit (R-2 = 0.9901-0.9998) correlated with RNA concentration. The multiplex gene expression profile indicated significantly downregulated levels of G protein-coupled receptor kinase interacting ArfGAP 2 (GIT2) and mitochondrial transcription termination factor (MTERF) genes in a lymph node-positive group of patients, with P values of 0.004 and 0.038, respectively. Therefore, this in-house method using multiple genes of interest might be an alternative tool for prediction of breast cancer metastasis.
引用
收藏
页码:10929 / 10936
页数:8
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