Saran Rashmi, Tiwari Ravindra K, Reddy Penagaluru Paradhanandan, Ahuja Yog Raj
Clinical Genetics Unit, Department of Pediatrics, All India Institute of Medical Sciences, New Delhi, India.
Oral Oncol. 2008 Apr;44(4):354-60. doi: 10.1016/j.oraloncology.2007.05.002. Epub 2007 Oct 23.
Oral cancer is a common malignancy, ranking first among all cancers in Western and Asian countries. Use of tobacco is regarded as a major risk factor, along with age and gender. Oral cancer is preceded by some benign lesions or conditions, which are termed pre-cancerous. Only one-third of people at the pre-cancerous stage of disease succumb to cancer. No biomarker is available to identify people with pre-cancerous lesions or conditions at high risk of developing cancer. The focus of this study was to explore such biomarkers. The study included 129 untreated people with cancer, 138 untreated people at the pre-cancerous stage and 176 control participants. For statistical analysis of this data, analysis of variance and t-test were used. Three biomarkers (i.e. micronucleus test [MNT], comet assay and challenge comet assay were used. MNT and comet assay were carried out on buccal epithelial cells. In addition, challenge comet assay was carried out on peripheral blood leucocytes by using mutagen MNNG sensitivity of DNA after DNA repair. A significant stepwise increase in the DNA damage (basal/MNNG-treated/post-repair) was observed in buccal epithelial cells and peripheral blood leucocytes from control to pre-cancer patients and from pre-cancer to cancer patients. Micronucleus frequency also increased in the same way. Considerable inter-individual and inter-cellular variability in DNA damage was observed, which increased from control to pre-cancer patients and from pre-cancer to cancer patients. The outliers among patients with pre-cancerous states were identified on the basis of more than mean +2 SD limits for comet tail length, as well as mean percentage of micronuclei. Hence, those participants whose cells showed high basal DNA damage, extreme sensitivity to MNNG and reduced repair were identified as high-risk individuals.
口腔癌是一种常见的恶性肿瘤,在西方国家和亚洲国家的所有癌症中位居首位。除年龄和性别外,吸烟被视为主要危险因素。口腔癌之前会出现一些良性病变或状况,这些被称为癌前病变。处于疾病癌前阶段的人中只有三分之一会患癌症。目前尚无生物标志物可用于识别具有癌前病变或状况且患癌风险高的人群。本研究的重点是探索此类生物标志物。该研究纳入了129名未经治疗的癌症患者、138名处于癌前阶段的未经治疗的患者以及176名对照参与者。对于这些数据的统计分析,使用了方差分析和t检验。使用了三种生物标志物(即微核试验[MNT]、彗星试验和挑战彗星试验)。MNT和彗星试验在颊上皮细胞上进行。此外,通过使用DNA修复后对诱变剂MNNG的敏感性,对外周血白细胞进行挑战彗星试验。在颊上皮细胞和外周血白细胞中,从对照到癌前患者以及从癌前到癌症患者,观察到DNA损伤(基础/经MNNG处理/修复后)有显著的逐步增加。微核频率也以相同方式增加。观察到DNA损伤存在相当大的个体间和细胞间变异性,从对照到癌前患者以及从癌前到癌症患者,这种变异性增加。根据彗星尾长超过平均值 +2标准差的界限以及微核的平均百分比,确定癌前状态患者中的异常值。因此,那些细胞显示出高基础DNA损伤、对MNNG极度敏感且修复能力降低的参与者被确定为高危个体。