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本文引用的文献

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Taxol resistance in breast cancer cells is mediated by the hippo pathway component TAZ and its downstream transcriptional targets Cyr61 and CTGF.乳腺癌细胞中的紫杉醇耐药是由 hippo 通路成分 TAZ 及其下游转录靶标 Cyr61 和 CTGF 介导的。
Cancer Res. 2011 Apr 1;71(7):2728-38. doi: 10.1158/0008-5472.CAN-10-2711. Epub 2011 Feb 24.
2
[DNA microarrays--perspective of application for drug effectivity and safety evaluation].[DNA微阵列——药物有效性和安全性评估的应用前景]
Postepy Biochem. 2008;54(1):107-15.
3
The p63/p73 network mediates chemosensitivity to cisplatin in a biologically defined subset of primary breast cancers.p63/p73网络在生物学定义的原发性乳腺癌亚群中介导对顺铂的化学敏感性。
J Clin Invest. 2007 May;117(5):1370-80. doi: 10.1172/JCI30866. Epub 2007 Apr 19.
4
Epigenetic inactivation of BRCA1 is associated with aberrant expression of CTCF and DNA methyltransferase (DNMT3B) in some sporadic breast tumours.在一些散发性乳腺肿瘤中,BRCA1的表观遗传失活与CTCF和DNA甲基转移酶(DNMT3B)的异常表达有关。
Eur J Cancer. 2007 Jan;43(1):210-9. doi: 10.1016/j.ejca.2006.09.002. Epub 2006 Oct 27.
5
Classification of ductal carcinoma in situ by gene expression profiling.通过基因表达谱对导管原位癌进行分类。
Breast Cancer Res. 2006;8(5):R61. doi: 10.1186/bcr1613.
6
Genetic expression profiles and chromosomal alterations in sporadic breast cancer in Mexican women.墨西哥女性散发性乳腺癌的基因表达谱和染色体改变
Cancer Genet Cytogenet. 2006 Oct 15;170(2):147-51. doi: 10.1016/j.cancergencyto.2006.06.002.
7
Regulation of transcription by synthetic DNA-bending agents.合成DNA弯曲剂对转录的调控。
Chembiochem. 2006 Nov;7(11):1715-21. doi: 10.1002/cbic.200600141.
8
AP-2gamma induces p21 expression, arrests cell cycle, and inhibits the tumor growth of human carcinoma cells.AP-2γ诱导p21表达,使细胞周期停滞,并抑制人癌细胞的肿瘤生长。
Neoplasia. 2006 Jul;8(7):568-77. doi: 10.1593/neo.06367.
9
HOXA5 regulates hMLH1 expression in breast cancer cells.HOXA5调节乳腺癌细胞中hMLH1的表达。
Neoplasia. 2006 Apr;8(4):250-8. doi: 10.1593/neo.05766.
10
AP-2alpha and AP-2gamma are transcriptional targets of p53 in human breast carcinoma cells.AP - 2α和AP - 2γ是人类乳腺癌细胞中p53的转录靶点。
Oncogene. 2006 Aug 31;25(39):5405-15. doi: 10.1038/sj.onc.1209534. Epub 2006 Apr 24.

检测紫杉醇对体外乳腺癌导管细胞中特定转录因子基因表达变化的影响。

The determination of changes in the expression of genes for selected specific transcriptional factors in in vitro ductal breast cancer cells under the influence of paclitaxel.

机构信息

Department of Biology and Genetics, Medical University of Lublin, 20-093, Lublin, Chodźki 4A, Poland.

出版信息

Cell Mol Biol Lett. 2011 Dec;16(4):610-24. doi: 10.2478/s11658-011-0026-8. Epub 2011 Sep 7.

DOI:10.2478/s11658-011-0026-8
PMID:21909792
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6275663/
Abstract

This study aimed to determine the changes in the expression of genes for selected specific transcriptional factors that have both activating and repressing functions in in vitro ductal breast cancer cells, under the influence of paclitaxel, applying the microarray technique. The cells are treated with 60 ng/ml and 300 ng/ml doses of paclitaxel that correspond to those applied in breast cancer therapy. About 60 ng/ml doses of paclitaxel cause a statistically significant increase in expression of all the 16 analysed genes coding transcriptional factors, ranging from 1.84-fold (for PO4F2) to 4.65-fold (for LMO4) (p < 0.05) in comparison with the control cells, and enhanced the taxane mechanism of action. The 300 ng/ml doses of paclitaxel cause a cytotoxic effect in the cells. In this article, we argue that these changes in gene expression values may constitute prognostic and predictive factors in ductal breast cancer therapy.

摘要

本研究旨在应用微阵列技术确定紫杉醇作用于体外乳腺癌细胞时,具有激活和抑制功能的特定转录因子基因表达的变化。用分别相当于乳腺癌治疗中应用剂量的 60ng/ml 和 300ng/ml 的紫杉醇处理细胞。约 60ng/ml 的紫杉醇剂量引起 16 个分析的编码转录因子的基因的表达均显著增加,范围从 1.84 倍(PO4F2)至 4.65 倍(LMO4)(p < 0.05),与对照细胞相比,并增强了紫杉烷的作用机制。300ng/ml 的紫杉醇剂量对细胞产生细胞毒性作用。在本文中,我们认为这些基因表达值的变化可能构成导管乳腺癌治疗的预后和预测因素。