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用人肿瘤异种移植模型中的碘脱氧尿苷标记和流式细胞术测量细胞增殖动力学:异质性研究以及不同计算方法与其他增殖测量方法的比较

Cell proliferation kinetics in human tumor xenografts measured with iododeoxyuridine labeling and flow cytometry: a study of heterogeneity and a comparison between different methods of calculation and other proliferation measurements.

作者信息

Perez L A, Dombkowski D, Efird J, Preffer F, Suit H D

机构信息

Edwin L. Steele Laboratory of Radiation Biology, Massachusetts General Hospital, Harvard Medical School, Boston 02114.

出版信息

Cancer Res. 1995 Jan 15;55(2):392-8.

PMID:7812972
Abstract

The influence of overall treatment time in the results of fractionated radiation treatment was initially established in experimental tumors and, subsequently, in the clinic. The availability of techniques (antibodies against halogenated thymidine analogues and flow cytometry) which permit determinations of the duration of the synthesis phase, the labeling index, and the tumor potential doubling time (Tpot) in a short period of time and requiring only a small biopsy of tumor tissue, has expanded interest in the relationship between tumor cell proliferation and response to irradiation. A valuable tool in the study of this relationship are human tumor xenografts. Previous studies have shown a substantial intratumoral heterogeneity in the determinations of Tpot. Different methods of calculation of the kinetic parameters have been published. We have conducted a heterogeneity analysis and an evaluation of the different calculation methods in order to define the validity of Tpot as a proliferation rate measurement in human tumor xenografts. Results show the intertumoral variability in Tpot [between different types of human tumor xenografts systems (coefficient of variation = 88.2%)] to be greater than mean intratumoral variation (coefficient of variation = 30.8%); this suggests that this variation is potentially adequate to serve as a predictor of response. The diverse calculation methods provided significantly different absolute values but not different tumor ranking, probably because the time interval between labeling and sampling was maintained, for all the samples, between 6 and 8 h. Our study has found significant differences between the labeling index and the S-phase fraction determined with the DNA profile in 9 out of 10 tumor types. No correlation was found between the DNA index of the tumors in this series and their proliferation rate.

摘要

分次放射治疗的总治疗时间对治疗结果的影响最初是在实验肿瘤中确定的,随后在临床中得到证实。现有技术(针对卤代胸腺嘧啶类似物的抗体和流式细胞术)能够在短时间内测定合成期持续时间、标记指数和肿瘤潜在倍增时间(Tpot),且仅需对肿瘤组织进行少量活检,这使得人们对肿瘤细胞增殖与放射反应之间的关系产生了更大兴趣。人肿瘤异种移植是研究这种关系的一种有价值的工具。先前的研究表明,在Tpot的测定中存在显著的肿瘤内异质性。已经发表了不同的动力学参数计算方法。我们进行了异质性分析并评估了不同的计算方法,以确定Tpot作为人肿瘤异种移植中增殖率测量指标的有效性。结果显示,Tpot在不同肿瘤间的变异性[在不同类型的人肿瘤异种移植系统之间(变异系数=88.2%)]大于肿瘤内平均变异性(变异系数=30.8%);这表明这种变异性可能足以作为反应的预测指标。不同的计算方法提供了显著不同的绝对值,但肿瘤排名没有差异,可能是因为所有样本的标记与取样之间的时间间隔保持在6至8小时之间。我们的研究发现,在10种肿瘤类型中的9种中,标记指数与通过DNA谱测定的S期分数之间存在显著差异。在该系列肿瘤中,未发现肿瘤的DNA指数与其增殖率之间存在相关性。

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