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本文引用的文献

1
Clinical DNA flow cytometry.临床DNA流式细胞术
Med Oncol Tumor Pharmacother. 1984;1(4):211-8. doi: 10.1007/BF02934525.
2
Cellular kinetics of invasive squamous carcinoma of the human cervix.人宫颈浸润性鳞状细胞癌的细胞动力学
Cancer Res. 1969 May;29(5):1082-8.
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A method to measure the duration of DNA synthesis and the potential doubling time from a single sample.一种从单个样本测量DNA合成持续时间和潜在倍增时间的方法。
Cytometry. 1985 Nov;6(6):620-6. doi: 10.1002/cyto.990060618.
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S-phase rate as a predictor of early recurrences in carcinoma of the uterine cervix.S期速率作为子宫颈癌早期复发的预测指标。
Anticancer Res. 1987 Jul-Aug;7(4B):807-10.
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Flow cytometric quantitation of DNA and c-myc oncoprotein in archival biopsies of uterine cervix neoplasia.子宫颈肿瘤存档活检组织中DNA和c-myc癌蛋白的流式细胞仪定量分析。
Br J Cancer. 1987 Mar;55(3):275-82. doi: 10.1038/bjc.1987.53.
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DNA flow cytometry and prognostic factors in 1331 frozen breast cancer specimens.1331例冷冻乳腺癌标本的DNA流式细胞术及预后因素
Cancer. 1988 Feb 1;61(3):420-7. doi: 10.1002/1097-0142(19880201)61:3<420::aid-cncr2820610303>3.0.co;2-0.
7
DNA ploidy, grade, and stage in prognosis of uterine cervical cancer.DNA倍体、分级及分期在子宫颈癌预后中的作用
Gynecol Oncol. 1989 Jan;32(1):4-7. doi: 10.1016/0090-8258(89)90840-8.
8
Cell proliferation kinetics in human solid tumors: relation to probability of metastatic dissemination and long-term survival.
Radiother Oncol. 1989 May;15(1):1-18. doi: 10.1016/0167-8140(89)90113-8.
9
DNA ploidy level as prognostic factor in low stage carcinoma of the uterine cervix.DNA倍体水平作为低期宫颈癌的预后因素
Gynecol Oncol. 1990 Nov;39(2):181-5. doi: 10.1016/0090-8258(90)90429-o.
10
Assessment of human tumour proliferation using bromodeoxyuridine--current status.使用溴脱氧尿苷评估人类肿瘤增殖——现状
Acta Oncol. 1991;30(8):903-10. doi: 10.3109/02841869109088242.

使用溴脱氧尿苷测量宫颈肿瘤中的细胞动力学。

Measurement of cell kinetics in cervical tumours using bromodeoxyuridine.

作者信息

Bolger B S, Cooke T G, Symonds R P, MacLean A B, Stanton P D

机构信息

University Department of Surgery, Glasgow Royal Infirmary, UK.

出版信息

Br J Cancer. 1993 Jul;68(1):166-71. doi: 10.1038/bjc.1993.307.

DOI:10.1038/bjc.1993.307
PMID:8318408
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1968308/
Abstract

The pre-treatment cell kinetics of 120 cervical tumours were assessed following the in vivo labelling with the thymidine analogue Bromodeoxyuridine (BrdUrd). In 89% both static and temporal kinetic parameters could be measured. Through the analysis of multiple biopsies from each tumour marked intra tumour heterogeneity was demonstrated. The median values for the most highly labelled sample analysed for each tumour were; S-phase duration (Ts) 12.1 h, BrdUrd labelling index (CLI) 9.5% and potential tumour doubling time 4.4 days. There was a significant elevation in CLI, but no difference in Ts, between tumour and non-neoplastic cervical tissue. There was a significant elevation in CLI, advanced stage and large size tumours. Although a significant elevation in CLI was found in aneuploid tumours this is likely to represent the systemic bias of the calculation methods, with no difference being seen between aneuploid and diploid tumours when BrdUrd labelling was measured with-out reference to the nuclei DNA content. The majority of these patients were treated with radiotherapy and cell kinetic data will be correlated with treatment response when adequate follow up has been achieved.

摘要

在用胸苷类似物溴脱氧尿苷(BrdUrd)进行体内标记后,评估了120例宫颈肿瘤的预处理细胞动力学。89%的病例能够测量静态和动态动力学参数。通过对每个肿瘤的多次活检分析,证实了肿瘤内的异质性。对每个肿瘤分析的标记程度最高的样本的中位数为:S期持续时间(Ts)12.1小时、BrdUrd标记指数(CLI)9.5%和潜在肿瘤倍增时间4.4天。肿瘤组织与非肿瘤性宫颈组织相比,CLI显著升高,但Ts无差异。CLI、晚期肿瘤和大尺寸肿瘤均显著升高。虽然在非整倍体肿瘤中发现CLI显著升高,但这可能代表计算方法的系统偏差,在不参考细胞核DNA含量测量BrdUrd标记时,非整倍体肿瘤和二倍体肿瘤之间未见差异。这些患者大多数接受了放射治疗,在获得充分随访后,细胞动力学数据将与治疗反应相关联。