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人表皮样癌HEp3/鸡胚模型中的早期自发转移:偶然定植的作用。

Early spontaneous metastasis in the human epidermoid carcinoma HEp3/chick embryo model: contribution of incidental colonization.

作者信息

Gordon J R, Quigley J P

出版信息

Int J Cancer. 1986 Sep 15;38(3):437-44. doi: 10.1002/ijc.2910380321.

Abstract

In the experimental model system where human tumor cells (HEp3) are implanted on the chorioallantoic membrane (CAM) of the chick embryo, metastasis of HEp3 cells to the embryonic lung occurs within a few days. Such rapidity in tumor dissemination makes this an attractive and potentially useful model for studying the metastatic process. The model, however, involves microvascular trauma at the site of implantation and thus tumor cells may accidentally enter the circulation during implantation or shortly thereafter. If these cells are the cause of the lung metastasis subsequently measured, the model would be in effect a colonization system and not a true, spontaneous metastasis system. The possible contribution of accidental lung colonization to secondary tumor growth was therefore critically examined in this model. In standard metastasis assays, HEp3 was inoculated onto the CAMs of 10-day embryos, which were then incubated for various periods of time. The embryos' lungs were passaged to a second group of CAMs, incubated for 7 days to allow expansion of any HEp3 cells present, and then assayed for HEp3 cells by both microscopy and measurement of human plasminogen activator (PA) activity. Metastasis was evidenced by PA values above background (30 mU/mg protein). Morphological analysis of HEp3 cells in the embryonic lung correlated closely with PA values. To focus on the early stages of tumor dissemination when colonization might occur, the primary tumor was surgically excised from 38 embryos at various intervals after tumor inoculation, and after the operation embryos were allowed to develop to day 17. This procedure increased estimated assay sensitivity down to the level of 1 to 10 cells per lung in embryos operated on within 2 days of inoculation. Median PA values in the transplanted lungs were 13, 3, 37, 1,290 and 3,765 mU/mg protein in the groups operated on at 4 hr, 1, 2, 3 and 4 days after inoculation, respectively. Thus very few or no HEp3 cells arrest and grow in the lungs during the first 24 to 48 hr, but extensive metastasis occurs by 72-96 hr. Accidental colonization therefore plays no major part in the rapid pulmonary spread of HEp3 in this model.

摘要

在将人类肿瘤细胞(HEp3)植入鸡胚绒毛尿囊膜(CAM)的实验模型系统中,HEp3细胞在几天内就会转移至胚胎肺。肿瘤扩散如此迅速,使得该模型成为研究转移过程的一个有吸引力且可能有用的模型。然而,该模型在植入部位涉及微血管损伤,因此肿瘤细胞可能在植入过程中或此后不久意外进入循环。如果这些细胞是随后检测到的肺转移的原因,那么该模型实际上将是一个定植系统,而非真正的自发转移系统。因此,在该模型中对意外肺定植对继发性肿瘤生长的可能作用进行了严格检验。在标准转移试验中,将HEp3接种到10日龄胚胎的CAM上,然后将胚胎孵育不同时间。将胚胎的肺移植到第二组CAM上,孵育7天以使存在的任何HEp3细胞得以增殖,然后通过显微镜检查和测量人纤溶酶原激活物(PA)活性来检测HEp3细胞。PA值高于背景值(30 mU/mg蛋白质)表明发生了转移。胚胎肺中HEp3细胞的形态学分析与PA值密切相关。为了关注可能发生定植的肿瘤扩散早期阶段,在接种肿瘤后的不同时间间隔,从38个胚胎中手术切除原发性肿瘤,术后让胚胎发育至17日龄。该程序将估计的检测灵敏度提高到接种后2天内进行手术的胚胎中每肺1至10个细胞的水平。接种后4小时、1天、2天、3天和4天进行手术的组中,移植肺中的PA值中位数分别为13、3、37、1290和3765 mU/mg蛋白质。因此,在最初的24至48小时内,很少有或没有HEp3细胞在肺中滞留并生长,但到72 - 96小时会发生广泛转移。因此,在该模型中,意外定植在HEp3迅速肺扩散中不起主要作用。

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