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雄激素剥夺治疗及前列腺癌雄激素非依赖性进展中的细胞凋亡和其他机制:综述

Apoptosis and other mechanisms in androgen ablation treatment and androgen independent progression of prostate cancer: a review.

作者信息

Westin P, Bergh A

机构信息

Department of Pathology, University of Umeå, Sweden.

出版信息

Cancer Detect Prev. 1998;22(5):476-84.

PMID:9727630
Abstract

Patients with advanced prostate cancer commonly present with disseminated disease. For these patients, androgen ablation is a first-line treatment. This mode of therapy usually has an initially palliative effect on tumor-related symptoms and slows growth, although virtually all tumors eventually relapse to an androgen-independent, more aggressively growing phenotype. However, surprisingly little is known about the actions mediating the initial palliative effect as well as the initiation of androgen-independent tumor growth. In this review, some current concepts on mechanisms of androgen ablation treatment and androgen-independent progression of prostate cancer is highlighted. Special attention is given to the involvement of apoptosis in these processes.

摘要

晚期前列腺癌患者通常表现为播散性疾病。对于这些患者,雄激素剥夺是一线治疗方法。这种治疗方式通常对肿瘤相关症状最初具有姑息作用,并减缓肿瘤生长,尽管几乎所有肿瘤最终都会复发为雄激素非依赖性、生长更具侵袭性的表型。然而,令人惊讶的是,对于介导初始姑息作用以及雄激素非依赖性肿瘤生长起始的作用了解甚少。在本综述中,重点介绍了一些关于雄激素剥夺治疗机制和前列腺癌雄激素非依赖性进展的当前概念。特别关注细胞凋亡在这些过程中的作用。

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Apoptosis and other mechanisms in androgen ablation treatment and androgen independent progression of prostate cancer: a review.雄激素剥夺治疗及前列腺癌雄激素非依赖性进展中的细胞凋亡和其他机制:综述
Cancer Detect Prev. 1998;22(5):476-84.
2
Sequencing hormonal ablation and radiotherapy in prostate cancer: a molecular and therapeutic prespective (Review).前列腺癌中激素消融与放疗的序贯治疗:分子与治疗学视角(综述)
Oncol Rep. 2002 Nov-Dec;9(6):1151-6.
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Sustained in vivo regression of Dunning H rat prostate cancers treated with combinations of androgen ablation and Trk tyrosine kinase inhibitors, CEP-751 (KT-6587) or CEP-701 (KT-5555).用雄激素去除与Trk酪氨酸激酶抑制剂CEP-751(KT-6587)或CEP-701(KT-5555)联合治疗的Dunning H大鼠前列腺癌在体内持续消退。
Cancer Res. 1999 May 15;59(10):2395-401.
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Cellular changes in prostate cancer cells induced by intermittent androgen suppression.间歇性雄激素抑制诱导的前列腺癌细胞的细胞变化。
Eur Urol. 2007 Sep;52(3):725-32. doi: 10.1016/j.eururo.2006.11.043. Epub 2006 Nov 28.
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Androgen receptor gene amplification at primary progression predicts response to combined androgen blockade as second line therapy for advanced prostate cancer.原发性进展时雄激素受体基因扩增可预测晚期前列腺癌二线治疗中联合雄激素阻断的疗效。
J Urol. 2000 Dec;164(6):1992-5.
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Alternative nonsteroidal antiandrogen therapy for advanced prostate cancer that relapsed after initial maximum androgen blockade.初始最大雄激素阻断治疗后复发的晚期前列腺癌的替代性非甾体抗雄激素治疗
J Urol. 2008 Sep;180(3):921-7. doi: 10.1016/j.juro.2008.05.045. Epub 2008 Jul 17.
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Amino-terminus domain of the androgen receptor as a molecular target to prevent the hormonal progression of prostate cancer.雄激素受体的氨基末端结构域作为预防前列腺癌激素进展的分子靶点。
J Cell Biochem. 2006 May 1;98(1):36-53. doi: 10.1002/jcb.20802.
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Increased Hsp27 after androgen ablation facilitates androgen-independent progression in prostate cancer via signal transducers and activators of transcription 3-mediated suppression of apoptosis.雄激素去除后热休克蛋白27增加通过转录信号转导子和激活子3介导的细胞凋亡抑制促进前列腺癌雄激素非依赖性进展。
Cancer Res. 2005 Dec 1;65(23):11083-93. doi: 10.1158/0008-5472.CAN-05-1840.
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Treatment options in androgen-independent prostate cancer.雄激素非依赖性前列腺癌的治疗选择。
Cancer Invest. 1999;17(2):137-44.
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Endocrine treatment of prostate cancer.前列腺癌的内分泌治疗
J Steroid Biochem Mol Biol. 2004 Nov;92(4):287-95. doi: 10.1016/j.jsbmb.2004.10.005. Epub 2004 Dec 31.

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Metabolomic profiling identifies biochemical pathways associated with castration-resistant prostate cancer.代谢组学分析确定了与去势抵抗性前列腺癌相关的生化途径。
J Proteome Res. 2014 Feb 7;13(2):1088-100. doi: 10.1021/pr401106h. Epub 2013 Dec 31.
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Mechanisms of acquired androgen independence during arsenic-induced malignant transformation of human prostate epithelial cells.砷诱导人前列腺上皮细胞恶性转化过程中获得性雄激素非依赖性的机制。
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Acquisition of androgen independence by human prostate epithelial cells during arsenic-induced malignant transformation.
在砷诱导的恶性转化过程中人类前列腺上皮细胞获得雄激素非依赖性
Environ Health Perspect. 2005 Sep;113(9):1134-9. doi: 10.1289/ehp.7832.
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Androgen-independent prostate cancer: potential role of androgen and ErbB receptor signal transduction crosstalk.雄激素非依赖性前列腺癌:雄激素与表皮生长因子受体(ErbB)信号转导相互作用的潜在作用
Neoplasia. 2003 Mar-Apr;5(2):99-109. doi: 10.1016/s1476-5586(03)80001-5.