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通过间期荧光原位杂交分析对42例前列腺肿瘤的触摸涂片进行Y染色体计数。

Y chromosome enumeration in touch preparations from 42 prostate tumors by interphase fluorescence in situ hybridization analysis.

作者信息

Tricoli J V

机构信息

Department of Radiation Oncology, Fox Chase Cancer Center, Philadelphia, PA 19111, USA.

出版信息

Cancer Genet Cytogenet. 1999 May;111(1):1-6. doi: 10.1016/s0165-4608(98)00212-x.

DOI:10.1016/s0165-4608(98)00212-x
PMID:10326583
Abstract

A change in Y chromosome number is but one of the many cytogenetic abnormalities reported in human prostate tumors. However, reports in the literature have varied regarding the frequency of Y loss or gain, whether it is restricted to the cancerous tissue, and its relation to the biology of the disease. The most frequently used materials for analysis of Y enumeration have been metaphase spreads from short-term cell cultures of prostate tumor tissue and paraffin-embedded tissue sections. Analysis of Y chromosome number by using metaphase spreads on short-term cultures can be misleading owing to clonal cell selection during the establishment of these cultures. This may result in an incomplete representation of the loss/gain pattern in the tumor as a whole. Studies using paraffin-embedded tissue sections can be complicated by apparent chromosome loss due to nuclear truncation as a result of tumor sectioning. In an attempt to circumvent these problems, we have used touch preparations from human prostate tumors to search for Y chromosome loss. Fluorescence in situ hybridization analysis was conducted by using a whole chromosome Y paint, with an alpha-satellite chromosome 3 probe as a control, on tumor samples from 42 patients ages 40-75. The results demonstrated a gain of Y in a single prostate tumor sample, with no convincing evidence for loss of the entire Y chromosome in any of the other 41 samples examined. The results suggest that loss of the entire Y chromosome is an infrequent event in prostate cancer.

摘要

Y染色体数量的改变只是人类前列腺肿瘤中报告的众多细胞遗传学异常之一。然而,文献中的报告在Y染色体丢失或增加的频率、是否仅限于癌组织及其与疾病生物学的关系方面存在差异。用于Y染色体计数分析的最常用材料是前列腺肿瘤组织短期细胞培养物的中期染色体铺展和石蜡包埋组织切片。由于在这些培养物建立过程中的克隆细胞选择,使用短期培养物的中期染色体铺展来分析Y染色体数量可能会产生误导。这可能导致整个肿瘤中丢失/增加模式的不完全呈现。使用石蜡包埋组织切片的研究可能会因肿瘤切片导致的核截断引起的明显染色体丢失而变得复杂。为了规避这些问题,我们使用了人类前列腺肿瘤的触片来寻找Y染色体丢失。对42名年龄在40至75岁患者的肿瘤样本,使用全染色体Y探针进行荧光原位杂交分析,并以α卫星染色体3探针作为对照。结果显示在单个前列腺肿瘤样本中Y染色体增加,在所检测的其他41个样本中均未发现令人信服的整个Y染色体丢失的证据。结果表明,整个Y染色体丢失在前列腺癌中是罕见事件。

相似文献

1
Y chromosome enumeration in touch preparations from 42 prostate tumors by interphase fluorescence in situ hybridization analysis.通过间期荧光原位杂交分析对42例前列腺肿瘤的触摸涂片进行Y染色体计数。
Cancer Genet Cytogenet. 1999 May;111(1):1-6. doi: 10.1016/s0165-4608(98)00212-x.
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Loss of the short arm of the Y chromosome in human prostate carcinoma.人类前列腺癌中Y染色体短臂缺失
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Defining the extent and nature of cytogenetic events in prostatic adenocarcinoma: paraffin FISH vs. metaphase analysis.确定前列腺腺癌中细胞遗传学事件的范围和性质:石蜡切片荧光原位杂交与中期分析
Cancer Genet Cytogenet. 1993 Aug;69(1):7-12. doi: 10.1016/0165-4608(93)90103-s.
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Lab Invest. 1997 Nov;77(5):437-48.
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Interphase cytogenetic analysis of prostatic carcinomas by use of nonisotopic in situ hybridization.应用非同位素原位杂交技术对前列腺癌进行间期细胞遗传学分析。
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Numerical abnormalities of chromosome 7 in human prostate cancer detected by fluorescence in situ hybridization (FISH) on paraffin-embedded tissue sections with centromere-specific DNA probes.使用着丝粒特异性DNA探针,通过荧光原位杂交(FISH)技术在石蜡包埋组织切片上检测人类前列腺癌中7号染色体的数目异常。
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Aneusomies of chromosomes 8 and Y detected by fluorescence in situ hybridization are prognostic markers for pathological stage C (pt3N0M0) prostate carcinoma.通过荧光原位杂交检测到的8号和Y染色体的非整倍体是病理分期为C期(pt3N0M0)前列腺癌的预后标志物。
Clin Cancer Res. 1996 Jan;2(1):137-45.

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Epigenetic Pattern on the Human Y Chromosome Is Evolutionarily Conserved.人类Y染色体上的表观遗传模式在进化上是保守的。
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2
Expression of a Y-located human proto-oncogene TSPY in a transgenic mouse model of prostate cancer.Y 染色体定位的人类原癌基因 TSPY 在前列腺癌转基因小鼠模型中的表达。
Cell Biosci. 2014 Feb 17;4(1):9. doi: 10.1186/2045-3701-4-9.
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Loss of Y-chromosome does not correlate with age at onset of head and neck carcinoma: a case-control study.
Y 染色体缺失与头颈部癌发病年龄无关:病例对照研究。
Braz J Med Biol Res. 2012 Feb;45(2):172-8. doi: 10.1590/s0100-879x2012007500004. Epub 2012 Jan 19.