El-Zein Randa A, Abdel-Rahman Shereen, Santee Kyle J, Yu Robert, Shete Sanjay
Department of Radiology, Houston Methodist Research Institute, Houston, TX, USA.
Cytogenet Genome Res. 2017;152(3):122-131. doi: 10.1159/000479809. Epub 2017 Sep 13.
Small cell lung cancer (SCLC) is a highly aggressive form of lung cancer. There is an urgent need to develop tools to identify individuals at high risk of developing SCLC. We have previously reported that the cytokinesis-blocked micronucleus (CBMN) assay is a strong predictor of non-small cell lung cancer (NSCLC). Here, we investigate the sensitivity of the CBMN endpoints as predictors of SCLC risk. We conducted the CBMN assay on SCLC patients (n = 216), NSCLC patients (n = 173), and healthy controls (n = 204). Per sample, 1,000 binucleated cells (BN) were scored, and 3 endpoints, micronuclei (BN-MN), nucleoplasmic bridges (BN-NPB), and nuclear buds(BN-BUD), were recorded. Spectral karyotyping was also conducted on SCLC patients (n = 116) and NSCLC patients (n = 137) to identify genomic regions unique to each disease. Significantly higher levels of CBMN endpoints were observed in both cancer groups compared to controls. BN-NPBs were significantly higher among SCLC patients compared to NSCLC patients (p < 0.001). Chromosomes 5 and 17 were associated with BN-MN, and chromosomes 5, 18, 20, and 22 were associated with BN-NPBs in SCLC patients. Given the high frequency of chromosome aberrations observed in SCLC, events such as reinsertion of the micronucleus and chromothripsis may be potential mechanisms for the genetic instability in these patients.
小细胞肺癌(SCLC)是一种侵袭性很强的肺癌形式。迫切需要开发工具来识别有患小细胞肺癌高风险的个体。我们之前曾报道,胞质分裂阻滞微核(CBMN)试验是预测非小细胞肺癌(NSCLC)的有力指标。在此,我们研究CBMN终点作为小细胞肺癌风险预测指标的敏感性。我们对小细胞肺癌患者(n = 216)、非小细胞肺癌患者(n = 173)和健康对照者(n = 204)进行了CBMN试验。每个样本对1000个双核细胞(BN)进行评分,并记录3个终点指标,即微核(BN-MN)、核质桥(BN-NPB)和核芽(BN-BUD)。我们还对小细胞肺癌患者(n = 116)和非小细胞肺癌患者(n = 137)进行了光谱核型分析,以确定每种疾病特有的基因组区域。与对照组相比,两个癌症组中CBMN终点指标水平均显著更高。与非小细胞肺癌患者相比,小细胞肺癌患者中的BN-NPB显著更高(p < 0.001)。在小细胞肺癌患者中,5号和17号染色体与BN-MN相关,5号、18号、20号和22号染色体与BN-NPB相关。鉴于在小细胞肺癌中观察到的染色体畸变频率较高,微核重新插入和染色体碎裂等事件可能是这些患者遗传不稳定的潜在机制。