Sood S, Patel F D, Ghosh S, Arora A, Dhaliwal L K, Srinivasan R
Molecular Pathology Laboratory, Department of Cytology and Gynecological Pathology, Postgraduate Institute of Medical Education and Research, Chandigarh, India.
Department of Radiotherapy and Oncology, Postgraduate Institute of Medical Education and Research, Chandigarh, India.
Clin Oncol (R Coll Radiol). 2015 Dec;27(12):720-7. doi: 10.1016/j.clon.2015.08.001. Epub 2015 Sep 4.
Locally advanced invasive cervical cancer [International Federation of Gynecology and Obstetrics (FIGO) IIB/III] is treated by chemoradiation. The response to treatment is variable within a given FIGO stage. Therefore, the aim of the present study was to evaluate the gene promoter methylation profile and corresponding transcript expression of a panel of six genes to identify genes which could predict the response of patients treated by chemoradiation.
In total, 100 patients with invasive cervical cancer in FIGO stage IIB/III who underwent chemoradiation treatment were evaluated. Ten patients developed systemic metastases during therapy and were excluded. On the basis of patient follow-up, 69 patients were chemoradiation-sensitive, whereas 21 were chemoradiation-resistant. Gene promoter methylation and gene expression was determined by TaqMan assay and quantitative real-time PCR, respectively, in tissue samples.
The methylation frequency of ESR1, BRCA1, RASSF1A, MLH1, MYOD1 and hTERT genes ranged from 40 to 70%. Univariate and hierarchical cluster analysis revealed that gene promoter methylation of MYOD1, ESR1 and hTERT could predict for chemoradiation response. A pattern of unmethylated MYOD1, unmethylated ESR1 and methylated hTERT promoter as well as lower ESR1 transcript levels predicted for chemoradiation resistance.
Methylation profiling of a panel of three genes that includes MYOD1, ESR1 and hTERT may be useful to predict the response of invasive cervical carcinoma patients treated with standard chemoradiation therapy.
局部晚期浸润性宫颈癌[国际妇产科联盟(FIGO)IIB/III期]采用放化疗进行治疗。在给定的FIGO分期内,治疗反应存在差异。因此,本研究的目的是评估一组六个基因的基因启动子甲基化谱及其相应的转录本表达,以鉴定能够预测放化疗患者反应的基因。
总共评估了100例接受放化疗的FIGO IIB/III期浸润性宫颈癌患者。10例患者在治疗期间发生全身转移,被排除在外。根据患者随访情况,69例患者对放化疗敏感,而21例患者对放化疗耐药。分别通过TaqMan分析和定量实时PCR测定组织样本中的基因启动子甲基化和基因表达。
ESR1、BRCA1、RASSF1A、MLH1、MYOD1和hTERT基因的甲基化频率在40%至70%之间。单因素和层次聚类分析显示,MYOD1、ESR1和hTERT的基因启动子甲基化可预测放化疗反应。MYOD1未甲基化、ESR1未甲基化、hTERT启动子甲基化以及ESR1转录本水平较低的模式可预测放化疗耐药。
包括MYOD1、ESR1和hTERT在内的三个基因的甲基化谱分析可能有助于预测接受标准放化疗的浸润性宫颈癌患者的反应。