[Establishment and characterization of a human lung adenocarcinoma cell line, Ch-Huang-1]
- PMID: 22613331
- PMCID: PMC6000122
- DOI: 10.3779/j.issn.1009-3419.2012.05.03
[Establishment and characterization of a human lung adenocarcinoma cell line, Ch-Huang-1]
Erratum in
- Zhongguo Fei Ai Za Zhi. 2012 Jul 20;15(7):408
Abstract
Background and objective: Lung cancer is a major worldwide health problem. The aim of this study is to establish a novel Chinese human lung adenocarcinoma cell line and examine its biological characteristics.
Methods: Lung adenocarcinoma specimens were freshly resected during surgery. The tissues were incubated in vitro and the cell line was named Ch-Huang-1. The biological characteristics of the cells were investigated by light microscopy, chromosome analysis, and transplantation experiment.
Results: Light microscopy revealed that cells from the primary tumor, Ch-Huang-1 cell line, and transplanted tumor possessed the characteristics of a malignant glandular epithelial tumor. The cell growth curve, doubling time, and mitotic index were also observed in vitro. Nuclear chromosome analysis revealed that the tumor was a subtriploid with a mode of 35-44 per cell. Tumor nodes were observed under the skin of nude mice by heterogenic transplantation.
Conclusion: The characteristics of the established cell line suggest that it is a newly established human adenocarcinoma cell line.
背景与目的: 肺癌是严重威胁人类生存和发展的恶性疾病之一,本研究旨在建立人肺腺癌细胞系,探讨其生物学特性,为进一步明确肺癌的发生机理,提供一个技术平台。
方法: 取人肺腺癌新鲜手术肿瘤标本,经组织块体外培养并克隆建系,命名为Ch-Huang-1。采用光镜、细胞生长曲线、染色体核型分析、克隆形成率及免疫缺陷小鼠成瘤实验对细胞系生物学特性进行分析。
结果: 细胞系及移植瘤标本证实具有腺癌恶性细胞特征。生长曲线呈S型,细胞群体倍增时间为36 h。分裂指数曲线为倒V字型,培养第30小时处于分裂期的细胞最多。克隆形成率为0.803%±0.078%。观察到肿瘤细胞染色体数目为亚三倍体,有明显的染色体异常。裸鼠皮下异种移植形成移植瘤。
结论: 根据细胞系特征显示该细胞系是一新建的肺腺癌细胞系。
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References
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- Ishikawa M, Kimura K, Tachibana T, et al. Establishment and characterization of a novel cell line derived from a human small cell lung carcinoma that secretes parathyroid hormone, parathyroid hormone-related protein, and pro-opiomelanocortin. Hum Cell. 2010;23(2):58–64. doi: 10.1111/huc.2010.23.issue-2. - DOI - PubMed
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