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本文引用的文献

1
Classifying the medulloblastoma: insights from morphology and molecular genetics.髓母细胞瘤的分类:来自形态学和分子遗传学的见解
Neuropathol Appl Neurobiol. 2002 Aug;28(4):257-82. doi: 10.1046/j.1365-2990.2002.00419.x.
2
Expression of telomerase genes in thyroid carcinoma.端粒酶基因在甲状腺癌中的表达。
Int J Oncol. 2002 Aug;21(2):265-72.
3
Prediction of survival in stage I lung carcinoma patients by telomerase function evaluation.通过端粒酶功能评估预测I期肺癌患者的生存率
Lab Invest. 2002 Jun;82(6):729-36. doi: 10.1097/01.lab.0000017165.26718.60.
4
Amplification of the telomerase reverse transcriptase (hTERT) gene in cervical carcinomas.宫颈癌中端粒酶逆转录酶(hTERT)基因的扩增。
Genes Chromosomes Cancer. 2002 Jul;34(3):269-75. doi: 10.1002/gcc.10071.
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Telomerase in brain tumors.脑肿瘤中的端粒酶
Childs Nerv Syst. 2002 Apr;18(3-4):112-7. doi: 10.1007/s00381-002-0562-7. Epub 2002 Feb 23.
6
Complex regulatory mechanisms of telomerase activity in normal and cancer cells: how can we apply them for cancer therapy?正常细胞和癌细胞中端粒酶活性的复杂调控机制:我们如何将其应用于癌症治疗?
Oncogene. 2002 Jan 21;21(4):688-97. doi: 10.1038/sj.onc.1205163.
7
Clinical utility of telomerase in cancer.端粒酶在癌症中的临床应用
Oncogene. 2002 Jan 21;21(4):643-9. doi: 10.1038/sj.onc.1205070.
8
hTERT gene dosage correlates with telomerase activity in human lung cancer cell lines.人端粒酶逆转录酶(hTERT)基因剂量与人类肺癌细胞系中的端粒酶活性相关。
Cancer Lett. 2002 Feb 8;176(1):81-91. doi: 10.1016/s0304-3835(01)00644-9.
9
Comparative genomic hybridization detects an increased number of chromosomal alterations in large cell/anaplastic medulloblastomas.比较基因组杂交检测发现,在大细胞/间变性髓母细胞瘤中存在更多数量的染色体改变。
Brain Pathol. 2002 Jan;12(1):36-44. doi: 10.1111/j.1750-3639.2002.tb00420.x.
10
Quantitative analysis of telomerase hTERT mRNA and telomerase activity in endometrioid adenocarcinoma and in normal endometrium.子宫内膜样腺癌及正常子宫内膜中端粒酶hTERT mRNA和端粒酶活性的定量分析。
Gynecol Oncol. 2002 Jan;84(1):120-5. doi: 10.1006/gyno.2001.6474.

端粒酶逆转录酶(hTERT)基因在中枢神经系统胚胎性肿瘤中的扩增及mRNA表达增加。

hTERT gene amplification and increased mRNA expression in central nervous system embryonal tumors.

作者信息

Fan Xing, Wang Yunyue, Kratz John, Brat Dan J, Robitaille Yves, Moghrabi Albert, Perlman Elizabeth J, Dang Chi V, Burger Peter C, Eberhart Charles G

机构信息

Johns Hopkins University School of Medicine, Baltimore, Maryland 21205, USA.

出版信息

Am J Pathol. 2003 Jun;162(6):1763-9. doi: 10.1016/S0002-9440(10)64311-8.

DOI:10.1016/S0002-9440(10)64311-8
PMID:12759234
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1868122/
Abstract

High-level gains at 5p15, a chromosomal region including the human telomerase catalytic protein subunit (hTERT) gene, have been documented in several medulloblastomas. We therefore analyzed hTERT gene dosage in a group of medulloblastomas and other embryonal brain tumors using differential PCR. Amplification of the hTERT locus was detected in 15 of 36 (42%) tumors examined. To correlate gene amplification with message level, we used real-time quantitative PCR to measure hTERT mRNA in 50 embryonal brain tumors. hTERT mRNA was detected in all but one of these cases, and mRNA level correlated significantly with gene dosage (r = 0.82). Log-rank analysis of survival data revealed a trend toward poor clinical outcomes in patients with medulloblastomas containing high hTERT mRNA levels, but clinical follow-up was relatively short and the association was not statistically significant (P = 0.078). Comparative genomic hybridization was used to further analyze the tumor with the greatest hTERT gene dosage and mRNA level, a recurrent medulloepithelioma. hTERT was amplified in the recurrent tumor but not in the primary lesion, suggesting this locus can be involved in tumor progression. Our data indicate that hTERT gene amplification is relatively common in embryonal brain tumors, and that increased expression of hTERT mRNA may be associated with biologically aggressive tumor behavior.

摘要

在几个成神经管细胞瘤中已记录到5号染色体短臂15区(5p15)的高水平扩增,该染色体区域包含人类端粒酶催化蛋白亚基(hTERT)基因。因此,我们使用差异PCR分析了一组成神经管细胞瘤和其他胚胎性脑肿瘤中的hTERT基因剂量。在所检测的36个肿瘤中有15个(42%)检测到hTERT基因座的扩增。为了将基因扩增与信使水平相关联,我们使用实时定量PCR来测量50个胚胎性脑肿瘤中的hTERT mRNA。除其中1例之外,所有这些病例均检测到hTERT mRNA,且mRNA水平与基因剂量显著相关(r = 0.82)。生存数据的对数秩分析显示,hTERT mRNA水平高的成神经管细胞瘤患者临床结局有较差的趋势,但临床随访时间相对较短,且这种关联无统计学意义(P = 0.078)。使用比较基因组杂交进一步分析hTERT基因剂量和mRNA水平最高的肿瘤,即复发性髓上皮瘤。hTERT在复发性肿瘤中扩增,但在原发性病变中未扩增,提示该基因座可能参与肿瘤进展。我们的数据表明,hTERT基因扩增在胚胎性脑肿瘤中相对常见,且hTERT mRNA表达增加可能与具有生物学侵袭性的肿瘤行为相关。