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癌胚抗原在体外及裸鼠体内监测人结肠腺癌肿瘤细胞SK-CO-1和HT-29生长中的作用

Carcino-embryonic antigen in monitoring the growth of human colon adenocarcinoma tumour cells SK-CO-1 and HT-29 in vitro and in nude mice.

作者信息

Sölétormos G, Fogh J M, Sehested-Hansen B, Spang-Thomsen M, Schiøler V, Dombernowsky P, Skovsgaard T

机构信息

Department of Oncology, Herlev Hospital, University of Copenhagen, Denmark.

出版信息

Eur J Cancer. 1997 Jan;33(1):108-14. doi: 10.1016/s0959-8049(96)00343-7.

Abstract

A set of experimental model systems were designed to investigate (a) the inter-relationship between growth of two human cancer cell lines (SK-CO-1, HT-29) and carcino-embryonic antigen (CEA) kinetics; and (b) whether neoplastic growth or CEA concentration is modulated by human growth hormone (hGH). We found that increasing CEA concentration depended on tumour burden. SK-CO-1 cells had the lowest growth rates but the highest rates of CEA production. The rate of CEA increase exceeded the growth rate of both SK-CO-1 and HT-29. hGH modulated neither neoplastic growth nor CEA production. In conclusion, our results suggest that experimental models may be useful for investigating the role of serological markers as monitors of increasing tumour burden. It will be of interest to investigate the performance of those model systems in examining the effect of cytotoxic agents in neoplastic growth.

摘要

设计了一组实验模型系统,以研究:(a)两种人类癌细胞系(SK - CO - 1、HT - 29)的生长与癌胚抗原(CEA)动力学之间的相互关系;以及(b)人类生长激素(hGH)是否会调节肿瘤生长或CEA浓度。我们发现,CEA浓度的增加取决于肿瘤负荷。SK - CO - 1细胞的生长速率最低,但CEA产生速率最高。CEA增加的速率超过了SK - CO - 1和HT - 29两者的生长速率。hGH既不调节肿瘤生长,也不调节CEA产生。总之,我们的结果表明,实验模型可能有助于研究血清学标志物作为肿瘤负荷增加监测指标的作用。研究这些模型系统在检测细胞毒性药物对肿瘤生长的影响方面的表现将是很有意义的。

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