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CBX3/异染色质蛋白1γ在非小细胞肺癌患者中显著上调。

CBX3/heterochromatin protein 1 gamma is significantly upregulated in patients with non-small cell lung cancer.

作者信息

Chang Shih-Chieh, Lai Yi-Chun, Chen Yen-Chung, Wang Nai-Kuan, Wang Wei-Shu, Lai Jiun-I

机构信息

School of Medicine, National Yang-Ming University, Taipei, Taiwan, Republic of China.

Division of Chest Medicine, Department of Medicine, National Yang-Ming University Hospital, Yilan, Taiwan, Republic of China.

出版信息

Asia Pac J Clin Oncol. 2018 Oct;14(5):e283-e288. doi: 10.1111/ajco.12820. Epub 2017 Nov 10.

DOI:10.1111/ajco.12820
PMID:29124886
Abstract

AIM

Lung cancer is typically categorized into small cell lung cancer (SCLC) and non-small cell lung cancer (NSCLC). NSCLC comprises of the majority of lung cancer with a poor prognosis in advanced cases. Transcriptional profiling studies, including microarrays and RNA-sequencing studies, have significantly enriched our knowledge of gene expression patterns in NSCLC. A recent transcriptional profiling study identified high prevalence of CBX3/HP1-gamma upregulation in human NSCLC samples. CBX3/HP1-gamma is an isoform of the heterochromatin protein 1 family, which plays a role in heterochromatin formation and is linked to cancer.

METHODS

We examined lung cancer samples from our hospital using immunohistochemistry for CBX3/HP1-gamma staining. We also analyzed publicly available databases of NSCLC transcriptional profiling to validate our results.

RESULTS

We identified a high prevalence (77.2%) of samples with positive CBX3/HP1-gamma staining by immunohistochemistry in NSCLC patient samples. Independently, we queried a publicly available dataset (GSE40419) containing RNA-seq data from 77 patients. Upregulation of CBX3/HP1-gamma in tumor samples was present in 60.2% of the patients. A similar correlation was also observed in the The Cancer Genome Atlas (TCGA) database. Interestingly, we discovered a highly significant association between positive CBX3/HP1-gamma staining and EGFR mutation in our patient samples (40 of 42 patients, P < 0.001). Treatment of EGFR mutant NSCLC cell lines with the EGFR inhibitor gefitinib failed to yield a change in CBX/HP1-gamma expression, suggesting that CBX/HP1-gamma expression may be independent of EGFR downstream signaling.

CONCLUSION

We report a significant upregulation of CBX3/HP1-gamma in NSCLC patients, and also a possible relationship between CBX3/HP1-gamma expression and EGFR mutation.

摘要

目的

肺癌通常分为小细胞肺癌(SCLC)和非小细胞肺癌(NSCLC)。NSCLC占肺癌的大多数,晚期病例预后较差。转录谱研究,包括微阵列和RNA测序研究,显著丰富了我们对NSCLC基因表达模式的认识。最近一项转录谱研究发现,CBX3/HP1-γ上调在人类NSCLC样本中普遍存在。CBX3/HP1-γ是异染色质蛋白1家族的一种异构体,在异染色质形成中起作用,并与癌症有关。

方法

我们使用免疫组织化学对CBX3/HP1-γ染色来检测我院的肺癌样本。我们还分析了公开可用的NSCLC转录谱数据库以验证我们的结果。

结果

通过免疫组织化学,我们在NSCLC患者样本中发现CBX3/HP1-γ染色阳性的样本比例很高(77.2%)。独立地,我们查询了一个包含77名患者RNA测序数据的公开数据集(GSE40419)。60.2%的患者肿瘤样本中存在CBX3/HP1-γ上调。在癌症基因组图谱(TCGA)数据库中也观察到了类似的相关性。有趣的是,我们在患者样本中发现CBX3/HP1-γ染色阳性与EGFR突变之间存在高度显著的关联(42名患者中有40名,P < 0.001)。用EGFR抑制剂吉非替尼治疗EGFR突变的NSCLC细胞系未能使CBX/HP1-γ表达发生变化,这表明CBX/HP1-γ表达可能独立于EGFR下游信号传导。

结论

我们报告了NSCLC患者中CBX3/HP1-γ的显著上调,以及CBX3/HP1-γ表达与EGFR突变之间可能存在的关系。

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