首页> 美国卫生研究院文献>British Journal of Cancer >A new human breast cancer cell line KPL-1 secretes tumour-associated antigens and grows rapidly in female athymic nude mice.
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A new human breast cancer cell line KPL-1 secretes tumour-associated antigens and grows rapidly in female athymic nude mice.

机译:KPL-1是一种新的人类乳腺癌细胞系可分泌与肿瘤相关的抗原并在雌性无胸腺裸鼠中快速生长。

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摘要

We recently established a new human breast cell line, designated KPL-1, which was derived from the malignant effusion of a patient with breast cancer. This cell line is highly tumorigenic and grows rapidly in female nude mice. Cytogenetic analysis indicated its human origin and revealed a hypertriploid modal number of chromosomes. Electron microscopic examination suggested that the KPL-1 cells are of epithelial origin. Immunohistochemical studies revealed that the cells express cytokeratin, carcinoembryonic antigen and CA 15-3. They also possess a large number of oestrogen receptors but not progesterone receptors. Interestingly, KPL-1 cells seem to grow oestrogen independently in vitro. No amplification of c-erbB-2, c-myc, H-ras and N-ras genes was detected. KPL-1 cells secrete a large amount of tissue polypeptide antigen (TPA). Although the secretion of CA 15-3 seemed to be constant throughout all cell growth phases, TPA secretion increased during the exponential growth phase and decreased during the plateau phase. Serum TPA levels significantly correlated with the volume of KPL-1 tumours transplanted into nude mice. These data suggest that this KPL-1 cell line may be useful for studying oestrogen-independent growth and the kinetics of tumour-associated antigens in vivo as well as in vitro.
机译:我们最近建立了一种新的人类乳腺癌细胞系,命名为KPL-1,该细胞系源于乳腺癌患者的恶性积液。该细胞系具有高度致瘤性,并在雌性裸鼠中快速生长。细胞遗传学分析表明其起源于人类并揭示了染色体的超三倍体模态数。电子显微镜检查表明KPL-1细胞是上皮来源的。免疫组织化学研究表明细胞表达细胞角蛋白,癌胚抗原和CA 15-3。它们还具有大量的雌激素受体,但不具有孕激素受体。有趣的是,KPL-1细胞似乎在体外独立生长雌激素。没有检测到c-erbB-2,c-myc,H-ras和N-ras基因的扩增。 KPL-1细胞分泌大量的组织多肽抗原(TPA)。尽管CA 15-3的分泌似乎在所有细胞生长期都是恒定的,但TPA分泌在指数生长期增加,而在平稳期减少。血清TPA水平与移植到裸鼠中的KPL-1肿瘤的体积显着相关。这些数据表明,该KPL-1细胞系可用于研究雌激素非依赖性生长以及体内外的肿瘤相关抗原的动力学。

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