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人膀胱癌中的DNA流式细胞术

DNA flow cytometry in human bladder carcinoma.

作者信息

Fosså S D, Thorud E, Pettersen E O, Shoaib M C, Scott-Knudsen O, Ous S

出版信息

Pathol Res Pract. 1986 Jun;181(3):291-5. doi: 10.1016/S0344-0338(86)80105-4.

DOI:10.1016/S0344-0338(86)80105-4
PMID:3748875
Abstract

The cell kinetic fractions (G0/G1; S; G2 + M) were evaluated by DNA flow cytometry (DNA FCM) in 102 biopsies from bladder carcinoma, previously untreated by cytotoxic therapy, and in 25 biopsies taken at least 3 months after prior treatment (chemotherapy, radiotherapy, surgery). Non-diploid DNA-stemlines were most often found in tumours of a high T category and of a high histopathological grade. Also the number of tumours with a fraction of cells in S-phase above 10% correlated with the clinical stage and histological grade. When the cytotoxic treatment preceded the actual biopsy by 3 months or more the distribution of stemline ploidies in the recurrent or residual tumours were similar to that seen in previously untreated patients. Furthermore, 4 of 5 individual muscle infiltrating bladder tumours treated with surgery, radiotherapy or systemic chemotherapy had the same stemline ploidy before and after treatment. The analysis of ploidy and cell kinetic parameters obtained from DNA FCM offers a possibility to evaluate the prognosis and the therapy effects in human bladder carcinoma.

摘要

通过DNA流式细胞术(DNA FCM)对102例未经细胞毒性治疗的膀胱癌活检样本以及25例在先前治疗(化疗、放疗、手术)后至少3个月采集的活检样本进行细胞动力学组分(G0/G1;S;G2 + M)评估。非二倍体DNA干系最常见于高T类别和高组织病理学分级的肿瘤中。此外,处于S期的细胞比例高于10%的肿瘤数量与临床分期和组织学分级相关。当细胞毒性治疗在实际活检前3个月或更长时间进行时,复发或残留肿瘤中干系倍体的分布与未经治疗患者中所见相似。此外,5例接受手术、放疗或全身化疗的浸润性膀胱肿瘤患者中有4例在治疗前后具有相同的干系倍体。从DNA FCM获得的倍体和细胞动力学参数分析为评估人类膀胱癌的预后和治疗效果提供了一种可能。

相似文献

1
DNA flow cytometry in human bladder carcinoma.人膀胱癌中的DNA流式细胞术
Pathol Res Pract. 1986 Jun;181(3):291-5. doi: 10.1016/S0344-0338(86)80105-4.
2
[The DNA content of bladder carcinoma in relation to pathologic grading, staging and prognosis: a flow cytometric study].[膀胱癌的DNA含量与病理分级、分期及预后的关系:一项流式细胞术研究]
Zhonghua Wai Ke Za Zhi. 1989 Nov;27(11):650-3, 700.
3
Ploidy aberrations and agar cloning ability of malignant cells from human bladder carcinoma.
Anticancer Res. 1984 May-Jun;4(3):113-6.
4
Colony formation in urinary bladder carcinoma. Relationship to DNA flow cytometry, stage and histopathology.膀胱癌中的集落形成。与DNA流式细胞术、分期及组织病理学的关系。
Anticancer Res. 1991 Mar-Apr;11(2):777-81.
5
[DNA ploidy and cell cycle phase analysis with flow cytometry in bladder wash. Preliminary experience].[膀胱冲洗液的DNA倍体及细胞周期阶段的流式细胞术分析。初步经验]
Arch Esp Urol. 2000 Jan-Feb;53(1):29-36.
6
[Combined flow cytometry determination of S-phase fraction and DNA ploidy is an independent prognostic factor in node-negative invasive breast carcinoma: review of a series of 271 patients with stage I and II breast cancer].[联合流式细胞术测定S期分数和DNA倍体是淋巴结阴性浸润性乳腺癌的独立预后因素:对271例I期和II期乳腺癌患者的系列研究回顾]
Cancer Radiother. 2005 Dec;9(8):575-86. doi: 10.1016/j.canrad.2005.09.016. Epub 2005 Oct 20.
7
Flow cytometry and interactive image cytometry in endometrial carcinoma. A comparative and prognostic study.
Anticancer Res. 1991 Mar-Apr;11(2):783-8.
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[Studies on nuclear DNA content in bladder cancers using flow cytometry].[应用流式细胞术对膀胱癌核DNA含量的研究]
Hokkaido Igaku Zasshi. 1996 Jan;71(1):45-53.
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[DNA ploidy pattern of flow cytometry as indicator of malignancy and prognosis in bladder cancer].
Nihon Rinsho. 1992 Oct;50(10):2426-31.
10
[DNA profile, recurrence rate and progression of superficial G2 cancer of the urinary bladder].
Urologe A. 1988 May;27(3):173-6.

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Int J Pancreatol. 1990 Aug-Nov;7(1-3):129-34. doi: 10.1007/BF02924229.