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Registered report: androgen receptor splice variants determine taxane sensitivity in prostate cancer.注册报告:雄激素受体剪接变体决定前列腺癌对紫杉烷的敏感性。
PeerJ. 2015 Sep 15;3:e1232. doi: 10.7717/peerj.1232. eCollection 2015.
2
Replication study: androgen receptor splice variants determine taxane sensitivity in prostate cancer.复制研究:雄激素受体剪接变体决定前列腺癌对紫杉烷的敏感性。
PeerJ. 2018 Apr 16;6:e4661. doi: 10.7717/peerj.4661. eCollection 2018.
3
Registered report: the androgen receptor induces a distinct transcriptional program in castration-resistant prostate cancer in man.注册报告:雄激素受体在男性去势抵抗性前列腺癌中诱导独特的转录程序。
PeerJ. 2015 Sep 15;3:e1231. doi: 10.7717/peerj.1231. eCollection 2015.
4
Androgen receptor splice variants determine taxane sensitivity in prostate cancer.雄激素受体剪接变异体决定前列腺癌对紫杉烷类药物的敏感性。
Cancer Res. 2014 Apr 15;74(8):2270-2282. doi: 10.1158/0008-5472.CAN-13-2876. Epub 2014 Feb 20.
5
Androgen Receptor Splice Variant 7 Drives the Growth of Castration Resistant Prostate Cancer without Being Involved in the Efficacy of Taxane Chemotherapy.雄激素受体剪接变体7驱动去势抵抗性前列腺癌的生长,且不参与紫杉烷化疗的疗效。
J Clin Med. 2018 Nov 16;7(11):444. doi: 10.3390/jcm7110444.
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Growth Inhibition by Testosterone in an Androgen Receptor Splice Variant-Driven Prostate Cancer Model.雄激素受体剪接变体驱动的前列腺癌模型中睾酮的生长抑制作用
Prostate. 2016 Dec;76(16):1536-1545. doi: 10.1002/pros.23238. Epub 2016 Jul 30.
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The RNA helicase DDX39B and its paralog DDX39A regulate androgen receptor splice variant AR-V7 generation.RNA解旋酶DDX39B及其旁系同源物DDX39A调节雄激素受体剪接变体AR-V7的产生。
Biochem Biophys Res Commun. 2017 Jan 29;483(1):271-276. doi: 10.1016/j.bbrc.2016.12.153. Epub 2016 Dec 23.
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Exploitation of the Androgen Receptor to Overcome Taxane Resistance in Advanced Prostate Cancer.雄激素受体的利用克服晚期前列腺癌中的紫杉烷耐药性。
Adv Cancer Res. 2015;127:123-58. doi: 10.1016/bs.acr.2015.03.001. Epub 2015 Mar 29.
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Androgen receptor splice variant 7 in castration-resistant prostate cancer: Clinical considerations.去势抵抗性前列腺癌中的雄激素受体剪接变体7:临床考量
Int J Urol. 2016 Aug;23(8):646-53. doi: 10.1111/iju.13134. Epub 2016 Jun 3.
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ARv7 Represses Tumor-Suppressor Genes in Castration-Resistant Prostate Cancer.ARv7 抑制去势抵抗性前列腺癌中的肿瘤抑制基因。
Cancer Cell. 2019 Mar 18;35(3):401-413.e6. doi: 10.1016/j.ccell.2019.01.008. Epub 2019 Feb 14.

引用本文的文献

1
Impact of taxanes on androgen receptor signaling.紫杉烷类药物对雄激素受体信号的影响。
Asian J Androl. 2019 May-Jun;21(3):249-252. doi: 10.4103/aja.aja_37_18.
2
Replication study: androgen receptor splice variants determine taxane sensitivity in prostate cancer.复制研究:雄激素受体剪接变体决定前列腺癌对紫杉烷的敏感性。
PeerJ. 2018 Apr 16;6:e4661. doi: 10.7717/peerj.4661. eCollection 2018.
3
Early abiraterone acetate treatment is beneficial in Japanese castration-resistant prostate cancer after failure of primary combined androgen blockade.在初次联合雄激素阻断治疗失败后,早期使用醋酸阿比特龙治疗对日本去势抵抗性前列腺癌有益。
Prostate Int. 2018 Mar;6(1):18-23. doi: 10.1016/j.prnil.2017.07.001. Epub 2017 Aug 9.

本文引用的文献

1
Exploitation of the Androgen Receptor to Overcome Taxane Resistance in Advanced Prostate Cancer.雄激素受体的利用克服晚期前列腺癌中的紫杉烷耐药性。
Adv Cancer Res. 2015;127:123-58. doi: 10.1016/bs.acr.2015.03.001. Epub 2015 Mar 29.
2
Are androgen receptor variants a substitute for the full-length receptor?雄激素受体变异体是否可以替代全长受体?
Nat Rev Urol. 2015 Mar;12(3):137-44. doi: 10.1038/nrurol.2015.13. Epub 2015 Feb 10.
3
N-terminal targeting of androgen receptor variant enhances response of castration resistant prostate cancer to taxane chemotherapy.雄激素受体变体的N端靶向增强去势抵抗性前列腺癌对紫杉烷化疗的反应。
Mol Oncol. 2014 Nov 15;9(3):628-39. doi: 10.1016/j.molonc.2014.10.014.
4
Biologic and clinical significance of androgen receptor variants in castration resistant prostate cancer.去势抵抗性前列腺癌中雄激素受体变体的生物学及临床意义
Endocr Relat Cancer. 2014 Aug;21(4):T87-T103. doi: 10.1530/ERC-13-0470. Epub 2014 May 23.
5
Targeting the androgen receptor pathway in castration-resistant prostate cancer: progresses and prospects.靶向去势抵抗性前列腺癌中的雄激素受体通路:进展与展望
Oncogene. 2015 Apr 2;34(14):1745-57. doi: 10.1038/onc.2014.115. Epub 2014 May 19.
6
The link between androgen receptor splice variants and castration-resistant prostate cancer.雄激素受体剪接变体与去势抵抗性前列腺癌之间的联系。
Horm Cancer. 2014 Aug;5(4):207-17. doi: 10.1007/s12672-014-0177-y. Epub 2014 May 6.
7
Androgen receptor splice variants determine taxane sensitivity in prostate cancer.雄激素受体剪接变异体决定前列腺癌对紫杉烷类药物的敏感性。
Cancer Res. 2014 Apr 15;74(8):2270-2282. doi: 10.1158/0008-5472.CAN-13-2876. Epub 2014 Feb 20.
8
Androgen receptor variants occur frequently in castration resistant prostate cancer metastases.雄激素受体变异体在去势抵抗性前列腺癌转移中经常发生。
PLoS One. 2011;6(11):e27970. doi: 10.1371/journal.pone.0027970. Epub 2011 Nov 17.
9
Resistance to CYP17A1 inhibition with abiraterone in castration-resistant prostate cancer: induction of steroidogenesis and androgen receptor splice variants.在去势抵抗性前列腺癌中,使用阿比特龙抑制 CYP17A1 产生耐药性:诱导甾体生成和雄激素受体剪接变体。
Clin Cancer Res. 2011 Sep 15;17(18):5913-25. doi: 10.1158/1078-0432.CCR-11-0728. Epub 2011 Aug 1.
10
Taxane-induced blockade to nuclear accumulation of the androgen receptor predicts clinical responses in metastatic prostate cancer.紫杉烷类诱导的雄激素受体核积累阻断可预测转移性前列腺癌的临床反应。
Cancer Res. 2011 Sep 15;71(18):6019-29. doi: 10.1158/0008-5472.CAN-11-1417. Epub 2011 Jul 28.

注册报告:雄激素受体剪接变体决定前列腺癌对紫杉烷的敏感性。

Registered report: androgen receptor splice variants determine taxane sensitivity in prostate cancer.

作者信息

Shan Xiaochuan, Danet-Desnoyers Gwenn, Fung Juan José, Kosaka Alan H, Tan Fraser, Perfito Nicole, Lomax Joelle, Iorns Elizabeth

机构信息

Stem Cell and Xenograft Core, Perelman School of Medicine, University of Pennsylvania , Philadelphia, PA , Unites States.

ProNovus Bioscience LLC , Mountain View, CA , United States.

出版信息

PeerJ. 2015 Sep 15;3:e1232. doi: 10.7717/peerj.1232. eCollection 2015.

DOI:10.7717/peerj.1232
PMID:26401448
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4579034/
Abstract

The Prostate Cancer Foundation-Movember Foundation Reproducibility Initiative seeks to address growing concerns about reproducibility in scientific research by conducting replications of recent papers in the field of prostate cancer. This Registered Report describes the proposed replication plan of key experiments from "Androgen Receptor Splice Variants Determine Taxane Sensitivity in Prostate Cancer" by Thadani-Mulero and colleagues (2014) published in Cancer Research in 2014. The experiment that will be replicated is reported in Fig. 6A. Thadani-Mulero and colleagues generated xenografts from two prostate cancer cell lines; LuCaP 86.2, which expresses predominantly the ARv567 splice variant of the androgen receptor (AR), and LuCaP 23.1, which expresses the full length AR as well as the ARv7 variant. Treatment of the tumors with the taxane docetaxel showed that the drug inhibited tumor growth of the LuCaP 86.2 cells but not of the LuCaP 23.1 cells, indicating that expression of splice variants of the AR can affect sensitivity to docetaxel. The Prostate Cancer Foundation-Movember Foundation Reproducibility Initiative is a collaboration between the Prostate Cancer Foundation, the Movember Foundation and Science Exchange, and the results of the replications will be published by PeerJ.

摘要

前列腺癌基金会 - 胡子月基金会可重复性倡议旨在通过对前列腺癌领域近期论文进行重复实验,来应对科学界对研究可重复性日益增长的担忧。本注册报告描述了对2014年发表在《癌症研究》上的Thadani - Mulero及其同事(2014年)所著论文《雄激素受体剪接变体决定前列腺癌对紫杉烷的敏感性》中关键实验的拟重复计划。将被重复的实验见图6A。Thadani - Mulero及其同事从两种前列腺癌细胞系生成了异种移植瘤;LuCaP 86.2主要表达雄激素受体(AR)的ARv567剪接变体,LuCaP 23.1表达全长AR以及ARv7变体。用紫杉烷多西他赛治疗肿瘤表明,该药物抑制了LuCaP 86.2细胞的肿瘤生长,但未抑制LuCaP 23.1细胞的肿瘤生长,这表明AR剪接变体的表达可影响对多西他赛的敏感性。前列腺癌基金会 - 胡子月基金会可重复性倡议是前列腺癌基金会、胡子月基金会和科学交流公司之间的合作,重复实验结果将由PeerJ发表。