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本文引用的文献

1
Ailanthone targets p23 to overcome MDV3100 resistance in castration-resistant prostate cancer.葶苈子酮通过靶向 p23 克服去势抵抗性前列腺癌中 MDV3100 的耐药性。
Nat Commun. 2016 Dec 13;7:13122. doi: 10.1038/ncomms13122.
2
The updated incidences and mortalities of major cancers in China, 2011.2011年中国主要癌症的最新发病率和死亡率。
Chin J Cancer. 2015 Sep 14;34(11):502-7. doi: 10.1186/s40880-015-0042-6.
3
Cancer statistics, 2015.癌症统计数据,2015 年。
CA Cancer J Clin. 2015 Jan-Feb;65(1):5-29. doi: 10.3322/caac.21254. Epub 2015 Jan 5.
4
AR-V7 and resistance to enzalutamide and abiraterone in prostate cancer.AR-V7 与前列腺癌中对恩杂鲁胺和阿比特龙的耐药性。
N Engl J Med. 2014 Sep 11;371(11):1028-38. doi: 10.1056/NEJMoa1315815. Epub 2014 Sep 3.
5
Lead- and drug-like compounds: the rule-of-five revolution.类铅化合物和类药物化合物:五规则革命
Drug Discov Today Technol. 2004 Dec;1(4):337-41. doi: 10.1016/j.ddtec.2004.11.007.
6
Androgen receptor splice variants mediate enzalutamide resistance in castration-resistant prostate cancer cell lines.雄激素受体剪接变异体介导恩杂鲁胺在去势抵抗性前列腺癌细胞系中的耐药性。
Cancer Res. 2013 Jan 15;73(2):483-9. doi: 10.1158/0008-5472.CAN-12-3630. Epub 2012 Nov 1.
7
Castration resistance in human prostate cancer is conferred by a frequently occurring androgen receptor splice variant.在人类前列腺癌中,雄激素受体剪接变体的频繁发生导致去势抵抗。
J Clin Invest. 2010 Aug;120(8):2715-30. doi: 10.1172/JCI41824. Epub 2010 Jul 19.
8
Molecular mechanisms of castration-resistant prostate cancer progression.去势抵抗性前列腺癌进展的分子机制。
Future Oncol. 2009 Nov;5(9):1403-13. doi: 10.2217/fon.09.117.
9
Quassinoids can induce mitochondrial membrane depolarisation and caspase 3 activation in human cells.苦木素类化合物可诱导人体细胞中的线粒体膜去极化和半胱天冬酶3激活。
Cell Death Differ. 2004 Dec;11 Suppl 2:S216-8. doi: 10.1038/sj.cdd.4401534.
10
Development of two androgen receptor assays using adenoviral transduction of MMTV-luc reporter and/or hAR for endocrine screening.利用MMTV-荧光素酶报告基因和/或人雄激素受体的腺病毒转导开发两种雄激素受体检测方法用于内分泌筛查。
Toxicol Sci. 2002 Mar;66(1):82-90. doi: 10.1093/toxsci/66.1.82.

Ailanthone: a new potential drug for castration-resistant prostate cancer.

作者信息

Peng Shihong, Yi Zhengfang, Liu Mingyao

机构信息

East China Normal University and Shanghai Fengxian District Central Hospital Joint Center for Translational Medicine, Shanghai Key Laboratory of Regulatory Biology, Institute of Biomedical Sciences and School of Life Sciences, East China Normal University, 500 Dongchuan Rd, Shanghai, 200241, P.R. China.

Department of Molecular and Cellular Medicine, Center for Cancer and Stem Cell Biology, Institute of Biosciences and Technology, Texas A&M University Health Sciences Center, Houston, TX, 77030, USA.

出版信息

Chin J Cancer. 2017 Mar 3;36(1):25. doi: 10.1186/s40880-017-0194-7.

DOI:10.1186/s40880-017-0194-7
PMID:28257652
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5336637/
Abstract
摘要