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. 2012 May;15(5):267-70.
doi: 10.3779/j.issn.1009-3419.2012.05.03.

[Establishment and characterization of a human lung adenocarcinoma cell line, Ch-Huang-1]

[Article in Chinese]
Affiliations

[Establishment and characterization of a human lung adenocarcinoma cell line, Ch-Huang-1]

[Article in Chinese]
Bailing Li et al. Zhongguo Fei Ai Za Zhi. 2012 May.

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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Figures

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1
倒置显微镜光镜观察:细胞多呈多角形,少数为梭形或圆形(×200)。A:原代培养细胞;B:传代细胞。 Most cells were polygonal and a few were spindle or round (×200). A: primary cultured cells; B: passage cells.
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细胞生长曲线图 Growth curve of cells line Ch-Huang-1
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细胞分裂指数分析 Analysis of cells division index
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细胞组织起源鉴定(DAB,×200) Identification of the cellular tissue origin (DAB, ×200)
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染色体核型分析 Chromosomal instability in Ch-Huang-1
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移植瘤癌细胞生长旺盛(HE,×40)。A:原代培养用组织块;B:移植瘤细胞。 Vigorous growth of transplanted tumor cells (HE, ×40). A: primary tissue culture cells; B: transplantation tumor cells.

References

    1. Jemal A, Siegel R, Ward E, et al. Cancer Statistics 2009. CA Cancer J Clin. 2009;59(4):225–249. doi: 10.3322/caac.20006. - DOI - PubMed
    1. Camerlingo R, Franco R, Tirino V, et al. Establishment and phenotypic characterization of the first human pulmonary blastoma cell line. Lung Cancer. 2011;72(1):23–31. doi: 10.1016/j.lungcan.2010.07.009. - DOI - PubMed
    1. 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
    1. Coburn MA, Brueggemann S, Bhatia S, et al. Establishment of a mammary carcinoma cell line from Syrian hamsters treated with N-methyl-N-nitrosourea. Cancer Lett. 2011;312(1):82–90. doi: 10.1016/j.canlet.2011.08.003. - DOI - PMC - PubMed
    1. Shin SH, Park SY, Kim MK, et al. Establishment and characterization of an immortalized human dermal papilla cell line. BMB Rep. 2011;44(8):512–516. doi: 10.5483/BMBRep.2011.44.8.512. - DOI - PubMed

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