Ludwig C, Harper J, Payne C, Nagle R, Bastert G, Trent J
Department of Internal Medicine of the University, Kantonsspital, Basel, Switzerland.
Anticancer Res. 1988 Jan-Feb;8(1):9-16.
We report here the detailed cellular and genetic analysis of two new human melanoma cell lines established from the same tumor biopsy. Although derived from the same tumor biopsy, the two lines differed in their method of in vitro culture establishment with one line (HA-A) grown first in agar culture and then transferred to liquid culture, while the second cell line (HA-L) was established directly from cells grown in liquid culture. Detailed characterization of both cell lines was performed using techniques to analyze their cytogenetic, surface marker, morphology (light and electron microscopy), growth (in agar and in nude mice), and drug sensitivity profiles in comparison to the original tumor biopsy. Our results revealed no significant biologic or genetic difference between the two cell lines established by different culture techniques. Our results suggest that in some cases agar culture prior to liquid culture may be useful in establishment of human tumor cell lines.
我们在此报告了从同一肿瘤活检样本中建立的两种新的人类黑色素瘤细胞系的详细细胞和遗传学分析。尽管这两种细胞系源自同一肿瘤活检样本,但它们的体外培养建立方法有所不同,其中一个细胞系(HA - A)先在琼脂培养中生长,然后转移至液体培养,而第二个细胞系(HA - L)则直接从液体培养中生长的细胞建立。使用多种技术对这两种细胞系进行了详细表征,以分析它们的细胞遗传学、表面标志物、形态学(光学和电子显微镜)、生长情况(在琼脂中和裸鼠体内)以及与原始肿瘤活检样本相比的药物敏感性谱。我们的结果显示,通过不同培养技术建立的这两种细胞系之间没有显著的生物学或遗传学差异。我们的结果表明,在某些情况下,液体培养前的琼脂培养可能有助于人类肿瘤细胞系的建立。