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高效液相色谱法测定抗前列腺癌药阿比特龙乙酸酯 被引量:2
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作者 龚爱琴 扈田进 贾志祥 《理化检验(化学分册)》 CAS CSCD 北大核心 2014年第8期983-986,共4页
提出了高效液相色谱法测定抗前列腺癌药阿比特龙乙酸酯的含量。色谱分离用Amethyst C18-H色谱柱(150mm×4.6mm,5μm),流动相为乙腈-磷酸盐缓冲溶液,流量为1.0mL·min-1,检测波长为236nm,进样量为20μL。阿比特龙乙酸酯的质量浓... 提出了高效液相色谱法测定抗前列腺癌药阿比特龙乙酸酯的含量。色谱分离用Amethyst C18-H色谱柱(150mm×4.6mm,5μm),流动相为乙腈-磷酸盐缓冲溶液,流量为1.0mL·min-1,检测波长为236nm,进样量为20μL。阿比特龙乙酸酯的质量浓度在0.1~1.2g·L-1范围内与峰面积呈线性关系,检出限(3S/N)为0.05mg·L-1。以空白样品为基体进行加标回收试验,所得平均加标回收率为99.6%,测定值的相对标准偏差(n=6)为0.17%。 展开更多
关键词 高效液相色谱法 阿比特龙乙酸酯 前列腺癌药
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抗前列腺癌药Atrasentan
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作者 林达 《药学进展》 CAS 2002年第5期316-317,共2页
关键词 前列腺癌药 ATRASENTAN
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03040 Atrix计划申请前列腺癌药
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作者 金伟华 《国外药讯》 2001年第3期22-22,共1页
关键词 Atrix 前列腺癌药 生物学标记物 拮抗剂
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与前列腺癌恩杂鲁胺耐药相关铁死亡基因的生物信息学分析 被引量:1
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作者 叶大文 张兆存 +2 位作者 赵海锋 王硕 姜先洲 《山东医药》 CAS 2022年第29期24-27,共4页
目的基于生物信息学方法分析与前列腺癌恩杂鲁胺耐药相关的铁死亡差异表达基因。方法从基因表达数据库(GEO)中下载恩杂鲁胺耐药与未耐药的前列腺癌细胞测序基因集(GSE104935、GSE78201),筛选差异表达基因;通过FerrDb数据库收集铁死亡相... 目的基于生物信息学方法分析与前列腺癌恩杂鲁胺耐药相关的铁死亡差异表达基因。方法从基因表达数据库(GEO)中下载恩杂鲁胺耐药与未耐药的前列腺癌细胞测序基因集(GSE104935、GSE78201),筛选差异表达基因;通过FerrDb数据库收集铁死亡相关基因。通过ImageGP维恩图工具将GEO数据库中差异表达基因及FerrDb数据库中铁死亡相关基因取交集,获得铁死亡相关恩杂鲁胺耐药前列腺癌的差异表达基因。将筛选出来的差异表达基因通过R软件进行GO功能(包括生物过程、分子功能、细胞成分)和KEGG作用通路富集分析。选取美国癌症研究所及美国人类基因组研究所收集处理的关于前列腺癌的测序数据和临床数据(TCGA-PRAD),通过R软件对铁死亡相关恩杂鲁胺耐药前列腺癌差异表达基因进行临床预后的单因素、多因素Cox回归分析,获得铁死亡相关恩杂鲁胺耐药前列腺癌的预后标志基因。用R软件在TCGA-PRAD队列中分析铁死亡相关恩杂鲁胺耐药前列腺癌预后标志基因的表达水平,Kaplan-Meier法比较预后标志基因高、低表达者的总生存期(OS)、无进展生存期(PFI)和疾病特异性生存期(DSS)。利用R软件绘制预测患者1、3、5年OS、PFI的受试者工作特征(ROC)曲线,通过曲线下面积(AUC)评价预测价值。结果从GEO、FerrDb数据库中共筛选获得铁死亡相关恩杂鲁胺耐药前列腺癌的差异表达基因31个。GO功能分析显示,铁死亡相关恩杂鲁胺耐药前列腺癌差异表达基因主要富集的生物过程为营养水平反应、细胞对外界刺激的反应、氧化应激反应等,主要富集的细胞成分为自噬体膜、次级溶酶体、自噬体等,主要富集的分子功能为类固醇脱氢酶活性、醛醇NADP+1-氧化还原酶、酰CoA连接酶活性等;KEGG作用通路分析显示,铁死亡相关恩杂鲁胺耐药前列腺癌差异表达基因主要富集的作用通路为花生四烯酸代谢、自噬、卡波西肉瘤相关疱疹病毒感染等。单因素、多因素Cox回归分析显示,LAMP2为铁死亡相关恩杂鲁胺耐药前列腺癌的预后标志基因。TCGA-PRAD队列中,LAMP2在前列腺癌组织中相对表达量低于正常组织(P<0.01),LAMP2低表达者OS、PFI均低于高表达者(P均<0.05),DSS与高表达者差异无统计学意义。ROC曲线结果显示,LAMP2预测前列腺癌患者1、3、5年OS的AUC分别为0.825、0.747、0.770,预测前列腺癌患者1、3、5年PFI的AUC分别为0.539、0.601、0.568。结论LAMP2、VEGFA、ACSF2等铁死亡相关恩杂鲁胺耐药前列腺癌差异表达基因主要富集在营养水平反应、细胞对外界刺激的反应、氧化应激反应等功能及花生四烯酸代谢、自噬、卡波西肉瘤相关疱疹病毒感染等作用通路。LAMP2为铁死亡相关恩杂鲁胺耐药前列腺癌的预后标志基因,LAMP2异常低表达是前列腺癌患者预后不良的独立危险因素,其对患者预后具有良好的预测价值。 展开更多
关键词 铁死亡 杂鲁胺耐前列腺 生物信息学 LAMP2 预后标志基因 分子机制
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新药研究与开发
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作者 黄世杰 《国外医学(药学分册)》 2006年第2期159-160,F0003,共3页
关键词 申报 研究与开发 生物技术公司 PROVENGE 晚期前列腺 Ⅲ期临床试验 前列腺癌药 免疫治疗 阿曲生坦 心脏毒性
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abarelix—depot—MⅢ期试验资料
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作者 景新 《国外药讯》 2000年第10期14-14,共1页
关键词 abarelix—depot—M Ⅲ期试验资料 AMGEN Praecis 前列腺癌药 激素治疗
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11046 Ferring公司的泌尿领域计划表
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作者 景新(摘) 《国外药讯》 2006年第11期21-22,共2页
Ferring制药公司说,其前列腺癌新药促性腺激素释放激素(GnRH)拮抗剂degarelix(FE106486)(Ⅰ)是其后期开发计划表中的关键产品。Ferring公司也在扩大其妇科药业务。(Ⅰ)是Decapepty[(Debiopharm公司的triptorelin)的第二代制... Ferring制药公司说,其前列腺癌新药促性腺激素释放激素(GnRH)拮抗剂degarelix(FE106486)(Ⅰ)是其后期开发计划表中的关键产品。Ferring公司也在扩大其妇科药业务。(Ⅰ)是Decapepty[(Debiopharm公司的triptorelin)的第二代制剂,与较老的抗前列腺癌药不同,它不会引起首次给药时初期的睾酮高峰。“GnRH拮抗剂如Decapeptyl在出现抑制作用前先有睾酮的上升,导致初期症状的恶化。(Ⅰ)的作用机理是能在给药后立即阻断睾酮分泌”。Ferring公司说,(Ⅰ)的作用持续时间也比别的抗前列腺癌药长,(Ⅰ)是第一批被开发的GnRH拮抗剂之一。 展开更多
关键词 GNRH拮抗剂 促性腺激素释放激素 前列腺癌药 pharm公司 泌尿 睾酮分泌 开发计划表 公司
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Casodex的临床及成本益处
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作者 曹菊 《国外药讯》 2005年第6期44-44,共1页
在《European Journal of Hospital Pharmacy》上发表的一篇文章强调了AstraZeneca公司的Casodex(bicalutamide,比卡鲁胺)(Ⅰ)在英国医疗系统中临床及成本益处。该药物可延缓局部晚期前列腺癌患者疾病的进展,并因此减少了该类患者终... 在《European Journal of Hospital Pharmacy》上发表的一篇文章强调了AstraZeneca公司的Casodex(bicalutamide,比卡鲁胺)(Ⅰ)在英国医疗系统中临床及成本益处。该药物可延缓局部晚期前列腺癌患者疾病的进展,并因此减少了该类患者终末期治疗所需的医疗资源。早期前列腺癌试验的结果显示,(I)不仅使接受放疗患者疾病进展的危险性减少42%,随诊观察及根治性前列腺切除患者的相应风险分别减少47%及29%,同时可以提高生活质量。 展开更多
关键词 Casodex 比卡鲁胺 前列腺癌药 医疗资源
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Analysis of drug use law and mechanism of prostate cancer based on data mining and network pharmacology
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作者 Yao Yang Ying Chen +1 位作者 Zhen-ning Yang Guo-wei Zhang 《TMR Modern Herbal Medicine》 2019年第3期140-150,共11页
Objective: Excavate the medication rule of traditional Chinese medicine in the treatment of prostate cancer, and predicting the biomolecular level mechanism of high-frequency drug compatibility. Methods: Relevant docu... Objective: Excavate the medication rule of traditional Chinese medicine in the treatment of prostate cancer, and predicting the biomolecular level mechanism of high-frequency drug compatibility. Methods: Relevant documents in CNKI, Wanfang Medical Network and VIP Chinese Biomedical Periodical Database Pubmed, EMbase were collected and collated systematically. Frequency statistics, association rule analysis and new party mining were carried out using TCMISSV2.5. BATMAN-TCM was used to analyze the interaction relationship and related pathways between high-frequency drug targets. Results: Huangqi (Astragalus membranaceus) was the single drug most used of the 102prescriptions included in the standard. There are 6 pairs of combinations with high confidence in association rule analysis. System entropy cluster analysis resulted in 20 core drug combinations and 9 new prescriptions. Through KEGG pathway analysis of Huangqi, Fuling (Poria cocos), Gancao (Glycyrrhiza uralensis) and Dihuang (Rehmannia glutinosa), it was found that the number of potential targets of the neural active ligand receptor rented pathway and purine metabolism pathway was the largest. Conclusions: Prostate cancer is mainly treated with deficiency-tonifying drugs, which are combined with drugs for promoting blood circulation, removing blood stasis, clearing heat, promoting diuresis, detoxifying and resolving hard mass. The mechanism of action of high-frequency traditional Chinese medicine may be realized by interfering with the neuroactive ligand receptor interaction pathway and purine metabolism pathway. 展开更多
关键词 prostate cancer medication law mechanism of action data mining network pharmacology
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Hepatotoxicity induced by cyproterone acetate:A report of three cases
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作者 Ioanna Savidou Melanie Deutsch +3 位作者 Aspasia S Soultati Dimitrios Koudouras Georgia Kafiri Spyridon P Dourakis 《World Journal of Gastroenterology》 SCIE CAS CSCD 2006年第46期7551-7555,共5页
Cyproterone acetate (CPA) is a steroidal synthetic progestagen and anti-androgenic compound widely administered in prostate cancer which has been evidentially correlated with a severe hepatotoxic potency. Three male p... Cyproterone acetate (CPA) is a steroidal synthetic progestagen and anti-androgenic compound widely administered in prostate cancer which has been evidentially correlated with a severe hepatotoxic potency. Three male patients aged 78-83 years are presented, in whom severe hepatotoxic reactions emerged after CPA administration. Patients were treated with CPA at the doses of 200-300 mg/d for malignant prostate disease for 3-12 mo prior to the acute manifestation of the hepatic disease. Clinical features compatible with mixed hepatocellular and cholestatic liver disease including jaundice, white stools and dark urine, manifested in all three cases whereas encephalopathy and ascites were present in two of the patients. Other primary causes of hepatotoxicity (alcohol consumption and viral hepatitis) were also verified in two cases, and in those patients biopsy findings revealed the presence of cirrhotic lesions in liver parenchyma. Discontinuation of the therapeutic agent led to the amelioration of the clinical profile in all the patients whereas a patient died 40 d after hospital admission due to sepsis, despite acute liver disease improvement. The current article highlights the hepatotoxic potency of a widely administered therapeutic agent and illustrates the importance of clinical surveillance especially in patients with previous hepatic diseases. Three relevant cases are reported and a review of the published literature is made. 展开更多
关键词 Cyproterone acetate Drug induced hepatotoxicity Prostate cancer Idiosyncratic drug reaction Hepatomitogen action
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Neuroendocrine differentiation in prostate cancer
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作者 Jingwen Wang Yang Yao 《The Chinese-German Journal of Clinical Oncology》 CAS 2008年第3期150-153,共4页
Hormonal therapy is an important treatment for advanced/metastatic prostate cancer. But it can induce neuroen-docrine(NE) differentiation in prostate cancer cells. These NE cells will secrete manifold neural peptide o... Hormonal therapy is an important treatment for advanced/metastatic prostate cancer. But it can induce neuroen-docrine(NE) differentiation in prostate cancer cells. These NE cells will secrete manifold neural peptide or hormones which can lead to androgen-independent growth of non-NE tumor cells. When this happens,hormonal therapy becomes useless and indicates bad prognosis. In this paper,the mechanism of neuroendocrine differentiation and its relationship with andro-gen-independent were reviewed. 展开更多
关键词 prostate cancer neuroendocrine differentiation drug resistance
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