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通过原位杂交检测膀胱癌中的染色体数目畸变。

Numerical chromosome aberrations in bladder cancer detected by in situ hybridization.

作者信息

Nemoto R, Nakamura I, Uchida K, Harada M

机构信息

Department of Urology, Tottori Prefectural Central Hospital, Japan.

出版信息

Br J Urol. 1995 Apr;75(4):470-6. doi: 10.1111/j.1464-410x.1995.tb07267.x.

DOI:10.1111/j.1464-410x.1995.tb07267.x
PMID:7788258
Abstract

OBJECTIVE

To investigate the relationship between interphase cytogenetics and the grade and stage of bladder cancer in patients with transitional cell carcinomas of the urinary bladder.

PATIENTS AND METHODS

By use of in situ hybridization with chromosome-specific DNA probes, the copy number of pericentromeric sequences on chromosomes 7, 10, 11, 17, 18, X and Y was detected within interphase nuclei in formalin-fixed and paraffin-embedded sections of the routinely processed bladder cancers from 20 patients. The percentage of hyperdiploid cells (three or more spots) was estimated using light microscopy.

RESULTS

The percentage of hyperdiploid cells for chromosomes 7, 11 and 17 was highly correlated with increasing tumour grade (P < 0.01, Spearman rank correlation) or increasing pathological stage (P < 0.01). The percentage of hyperdiploid cells for chromosome Y was not correlated with either grade or stage (P > 0.05). As high tumour grade and stage are both indicative of more aggressive tumour behaviour and a worse prognosis, these findings suggest that the percentage of hyperdiploid cells, especially for chromosomes 7, 11 and 17, may be highly predictive of bladder tumour aggressiveness.

CONCLUSION

These preliminary results suggest that measurement of numerical chromosome aberrations using in situ hybridization in bladder cancer may offer a new objective and quantitative assay of the biological potential of individual tumours.

摘要

目的

研究膀胱移行细胞癌患者间期细胞遗传学与膀胱癌分级和分期之间的关系。

患者与方法

通过使用染色体特异性DNA探针进行原位杂交,在20例患者常规处理的膀胱癌福尔马林固定石蜡包埋切片的间期核内,检测7、10、11、17、18、X和Y染色体着丝粒周围序列的拷贝数。使用光学显微镜估计超二倍体细胞(三个或更多位点)的百分比。

结果

7、11和17号染色体超二倍体细胞的百分比与肿瘤分级增加(P < 0.01,Spearman等级相关性)或病理分期增加(P < 0.01)高度相关。Y染色体超二倍体细胞的百分比与分级或分期均无相关性(P > 0.05)。由于高肿瘤分级和分期均表明肿瘤行为更具侵袭性且预后更差,这些发现提示超二倍体细胞的百分比,尤其是7、11和17号染色体的,可能高度预测膀胱肿瘤的侵袭性。

结论

这些初步结果表明,在膀胱癌中使用原位杂交测量染色体数目畸变可能为个体肿瘤的生物学潜能提供一种新的客观定量检测方法。

相似文献

1
Numerical chromosome aberrations in bladder cancer detected by in situ hybridization.通过原位杂交检测膀胱癌中的染色体数目畸变。
Br J Urol. 1995 Apr;75(4):470-6. doi: 10.1111/j.1464-410x.1995.tb07267.x.
2
[A comparative study of DNA measurement of bladder cancer from image cytometry and chromosome aberration in in situ hybridization].[图像细胞术检测膀胱癌DNA与原位杂交染色体畸变的比较研究]
Gan To Kagaku Ryoho. 1995 Jun;22 Suppl 2:153-7.
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Centromeric copy number of chromosome 7 is strongly correlated with tumor grade and labeling index in human bladder cancer.在人类膀胱癌中,7号染色体着丝粒拷贝数与肿瘤分级和标记指数密切相关。
Cancer Res. 1991 Jul 15;51(14):3807-13.
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Detection of numerical chromosome aberrations using in situ hybridization in paraffin sections of routinely processed bladder cancers.在常规处理的膀胱癌石蜡切片中使用原位杂交检测染色体数目畸变
Mod Pathol. 1991 Jul;4(4):503-13.
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Genomic heterogeneity in bladder cancer as detected by fluorescence in situ hybridization.通过荧光原位杂交检测到的膀胱癌基因组异质性。
Br J Urol. 1996 Nov;78(5):699-703. doi: 10.1046/j.1464-410x.1996.01786.x.
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Numeric aberration of chromosome 17 is strongly correlated with p53 overexpression, tumor proliferation and histopathology in human bladder cancer.17号染色体的数值畸变与人类膀胱癌中的p53过表达、肿瘤增殖及组织病理学密切相关。
Int J Urol. 1998 Jul;5(4):317-23. doi: 10.1111/j.1442-2042.1998.tb00358.x.
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Numerical aberrations of chromosome 8 and allelic loss at 8p in non-muscle-invasive urothelial carcinomas of the urinary bladder.膀胱非肌层浸润性尿路上皮癌中8号染色体的数值畸变及8p等位基因缺失
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[Detection of numerical chromosome aberrations in urologic malignancies using in situ hybridization from formarin-fixed paraffin sections].[利用福尔马林固定石蜡切片原位杂交技术检测泌尿系统恶性肿瘤中的染色体数目畸变]
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Chromosomal aberrations in transitional cell carcinoma: its correlation with tumor behavior.移行细胞癌中的染色体畸变:其与肿瘤行为的相关性。
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