anticancer杂志

anticancer杂志

期刊名 anticancer research 出版周期: 月刊
中科院杂志分区 肿瘤学分类下的 4 区期刊

近四年影响因子:
2013年度 2012年度 2011年度 2010年度
1.872 1.713 1.725 1.656

出版社或管理机构 杂志由 INT INST ANTICANCER RESEARCH 出版或管理。 ISSN号：0250-7005
杂志简介/稿件收录要求 Anticancer Research (AR) publishes high quality works and reviews on all aspects of experimental and clinical cancer research. AR preferentially publishes papers advancing the understanding of cancer causation, and papers applying the results of basic research to cancer diagnosis, prognosis and therapy.

那位兄弟 帮我找份 药物销售的外文文献啊 高分

【分享】有奖翻译外文文献摘要（药物专区）

药物专区

这篇综述重点阐述了藻类中具有食用和保健价值的各种长链不饱和脂肪酸的研究状况。

文题：Lipids and lipid metabolism in eukaryotic algae
作者：Guschina, I. A. Harwood, J. L.
杂志全名：Progress in Lipid Research
年份，卷（期）: 起止页码： 2006, Vol 45, No 2, 160-186
英文摘要：
Eukaryotic algae are a very diverse group of organisms which inhabit a huge range of ecosystems from the Antarctic to deserts. They account for over half the primary productivity at the base of the food chain. In recent years studies on the lipid biochemistry of algae has shifted from experiments with a few model organisms to encompass a much larger number of, often unusual, algae. This has led to the discovery of new compounds, including major membrane components, as well as the elucidation of lipid signalling pathways. A major drive in recent research have been attempts to discover genes that code for expression of the various proteins involved in the production of very long-chain polyunsaturated fatty acids such as arachidonic, eicosapentaenoic and docosahexaenoic acids. Such work is described here together with information about how environmental factors, such as light, temperature or minerals, can change algal lipid metabolism and how adaptation may take place.
中文译文：
真核藻类中脂类及其代谢研究综述
真核藻类是一大类具有多样性的种群，它的覆盖范围很广的，栖息地遍及从南极圈到沙漠的各类生态系统。藻类占据了初级生产力的一半以上，成为食物链的基础。近年来，人们对藻细胞中脂类物质的生化研究已经从很少的几种模式微生物其他物种拓展，开展了对众多物种包括一些非常见藻类的研究。这些研究带来了许多新的化合物的发现，包括一些细胞膜的主要组分、以及脂类信号转导途径中的重要分子。这些研究的主要目标是寻找这些长链不饱和脂肪酸合成蛋白的编码基因。同时本文中还综述了环境因子（例如光、温度、微量元素）对藻类脂肪代谢的影响以及藻细胞的应答机制的相关研究信息。

影响因子（2005） 8.810
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共翻译了5篇，其中三篇综述，两篇研究性文章。都是有关海洋药物方面的，大部分是海洋抗癌药物。尽我所能进行了翻译，部分词汇查不到中文译名，就没有翻译。

个人认为第四篇文章的水平很高，这时发表在PNAS上面的文章，一般化学类的文章，JACS（影响因子7左右）是顶级的杂志了。做的是海洋复杂天然产物的构型构象确定，该化合物是一个含侧链的25元环的大环内酯。类似于沙海葵毒素，研究方法也是从结构的片断开始，逐步确定其立体结构，当然本文所研究的结构没有沙海葵毒素（由129个碳原子组成的聚醚化合物，分子量为2677，含有40个羟基和8个甲基）那么复杂。虽然本文没有确定整个结构的立体结构，但本文的研究为确定该类型化合物的立体结构打下了基础。

第一篇（文章类型：Review）

文题：Marine pharmacology in 2003–2004: Anti-tumour and cytotoxic compounds
作者：Alejandro M.S. Mayer, Kirk R. Gustafson
杂志全名：European Journal of Cancer（IF for 2005：3.706；IF for 2005：3.302）
年份，卷（期）: 起止页码：42 (2006 )：2241－2270
英文摘要：During 2003 and 2004, marine pharmacology research directed towards the discovery and development of novel anti-tumour agents was published in 163 peer-reviewed articles. The purpose of this reviewis to present a structured assessment of the anti-tumour and cytotoxic properties of 150 marine natural products, many of which are novel compounds that belong to diverse structural classes, including polyketides, terpenes, steroids and peptides. The organisms yielding these bioactive marine compounds include invertebrate animals, algae, fungi and bacteria. Anti-tumour pharmacological studies were conducted with 31 structurally defined marine natural products in a number of experimental and clinical models that further defined their mechanisms of action. Particularly potent in vitro cytotoxicity data generated with murine and human tumour cell lines was reported for 119 novel marine chemicals with as yet undetermined mechanisms of action. Noteworthy is the fact that marine anti-cancer research was sustained by a global collaborative effort, involving researchers from Australia, Austria, Canada, China, Egypt, France, Germany, Italy, Japan, Mexico, the Netherlands, New Zealand, Papua New Guinea, the Philippines, South Africa, South Korea, Spain, Switzerland, Taiwan, Thailand and the United States of America (USA). Finally, this 2003–2004 overview of the marinepharmacology literature highlights the fact that the discovery of novel marine anti-tumour agents continued at the same pace as during 1998–2002.

中文译文(包括题目)：
2003-2004海洋药理学：抗肿瘤及细胞毒化合物
2003至2004年度，研究方向为寻找发现新抗肿瘤药物的海洋药理学论文总共发表了163篇。 本综述旨在对大约150个海洋天然产物的抗肿瘤及细胞毒活性进行化学结构上的分析，其中许多化合物属于不同的结构类型，包括聚酮化合物、帖类、甾体以及多肽。产生这些活性化合物的生物包括无脊椎动物、海藻、真菌和细菌。在大量的实验及临床模型上，研究人员对31个结构明确的海洋天然产物进行了抗肿瘤药理研究，这样的研究进一步明确了其作用机制。据报道，共有119种新的海洋化合物在体外对鼠或人类肿瘤细胞有特别强的细胞毒作用，作用机制尚未阐明。值得注意的是，全球许多国家合作进行海洋抗肿瘤药物研究，包括澳大利亚、奥地利、加拿大、埃及、法国、德国、意大利、日本、墨西哥、荷兰、新西兰、新几内亚、菲律宾、南非、南朝鲜、西班牙、瑞士、台湾、泰国及美国。最后，2003－2004年的海洋药理学研究综述表明发现新抗肿瘤化合物的速度与1998－2002期间一致。

第二篇（文章类型：Review）
文题：Indole alkaloid marine natural products: An established source of cancer drug leads with considerable promise for the control of parasitic, neurological and other diseases
作者：Waseem Gul, Mark T. Hamann
杂志全名：Life Sciences（IF for 2005：2.512；IF for 2005：2.158）
年份，卷（期）: 起止页码：78 (2005)：442－453
英文摘要：The marine environment produces natural products from a variety of structural classes exhibiting activity against numerous disease targets. Historically marine natural products have largely been explored as anticancer agents. The indole alkaloids are a class of marine natural products that show unique promise in the development of new drug leads. This report reviews the literature on indole alkaloids of marine origin and also highlights our own research. Specific biological activities of indole alkaloids presented here include: cytotoxicity, antiviral, antiparasitic, antiinflammatory, serotonin antagonism, Ca-releasing, calmodulin antagonism, and other pharmacological activities.

中文译文(包括题目)：
吲哚生物碱海洋天然产物：明确的抗癌药物先导化合物库，在治疗寄生虫病、神经病及其它疾病具有良好的前景

海洋产生了大量的各种结构类型的天然产物，它们作用于不同的疾病靶点。历史上，对海洋天然产物的研究大都是在抗癌方向。海洋中的吲哚类生物碱在作为新药先导化合物方面，具有独一无二的良好前景。本文综述了有关海洋来源的吲哚生物碱的文献，同时也包括了我们自己的研究。在这里，我们展示了吲哚类生物碱的独特生物活性，包括：细胞毒、抗病毒、抗寄生虫、抗炎、拮抗5-羟色胺、钙释放、拮抗钙调蛋白及其他药理活性。

第三篇（文章类型：Review）
文题：Marine natural products as anticancer drugs
作者：T. Luke Simmons, Eric Andrianasolo, Kerry McPhail, Patricia Flatt, and William H. Gerwick
杂志全名：Molecular Cancer Therapeutics（IF for 2005：5.171；IF for 2004：5.242）
年份，卷（期）: 起止页码：2005;4(2)：333–42
英文摘要：The chemical and biological diversity of the marine environment is immeasurable and therefore is an extraordinary resource for the discovery of new anticancer drugs. Recent technological and methodologic advances in structure elucidation, organic synthesis, and biological assay have resulted in the isolation and clinical evaluation of various novel anticancer agents. These compounds range in structural class from simple linear peptides, such as dolastatin 10, to complex macrocyclic polyethers, such as halichondrin B; equally as diverse are the molecular modes of action by which these molecules impart their biological activity. This review highlights several marine natural products and their synthetic derivatives that are currently undergoing clinical evaluation as anticancer drugs.

中文译文(包括题目)：
作为抗肿瘤药物的海洋天然产物

海洋环境的化学与生物多样性是无法衡量的，因此海洋是发现新抗癌药物的特别资源库。今年来，结构鉴定、有机合成、生物分析在技术及方法学方面的发展带动了各种新抗癌药物的分离及临床评价。这些化合物的结构各异，从简单的线性多肽如多拉司他汀10，到复杂的大环聚醚类化合物如软海绵素B。有如结构差异，这些化合物赖以传递作用的分子模式也各不相同。本文综述了一些来自海洋的天然产物及其合成衍生物，目前这些化合物正作为抗癌药进行临床评价。

第四篇（文章类型：research article）
文题：Synthesis of antimicrofilament marine macrolides: Synthesis and configurational assignment of a C5–C16 degradation fragment of reidispongiolide A
作者：Ian Paterson, Robert Britton, Kate Ashton, Henner Knust, and Jonathan Stafford
杂志全名：proceedings of the national academy of sciences of the united states of america
年份，卷（期）: 起止页码：2004 August 17; 101(33): 11986–11991.
英文摘要：Reidispongiolide A is a representative member of the sphinxolide/reidispongiolide group of cytotoxic 26-membered macrolides of marine origin. By interacting with actin in the cell cytoskeleton, the reidispongiolides and sphinxolides are potent microfilament destabilizing agents that represent a promising mechanism of action for developing novel anticancer drugs. An aldol-based synthesis of a library of diastereomers of C8–C16 and C5–C16 fragments and detailed NMR comparison with a reported degradation fragment enabled a configurational assignment for a major part of the reidispongiolide macrocyclic core, thus setting a solid foundation for ongoing synthetic efforts.

中文译文(包括题目)：
具抗微丝活性的海洋大环内酯合成：reidispongiolide A分解片断C5–C16的合成及构象指定

Reidispongiolide A是来自海洋的含sphinxolide/reidispongiolide 基团的26元环大环内酯类化合物的代表。通过与细胞骨架的肌动蛋白相互作用，这些大环内酯类化合物使得微丝失稳，这是研发新抗癌药物的有望机制。从丁间醇醛开始，合成了C8-C16及C5–C16的非对映体库，并将其NMR数据与一已报道的分解片断进行详细的比较，从而指定了reidispongiolide大环母核主要部分的构象，为后续的合成工作提供了坚实的基础。

第五篇（文章类型：research article）
文题：Aureoverticillactam, a novel 22-atom macrocyclic lactam from the marine actinomycete Streptomyces aureoverticillatus.
作者：Scott S. Mitchell, Benjamin Nicholson, Sy Teisan, Kin S. Lam, and Barbara C. M. Potts
杂志全名：journal of natural products（IF for 2005：2.202； IF for 2004：2.267）
年份，卷（期）: 起止页码：2004 Aug;67:1400-2.
英文摘要：During the course of our screening program designed to discover novel anticancer and anti-infective agents from marine microorganisms, a strain of Streptomyces aureoverticillatus (NPS001583) isolated from a marine sediment was found to produce a novel macrocyclic lactam with cytotoxicity against various tumor cell lines. Using extensive MS, UV, and NMR spectral analyses, the structure has been established as compound 1, aureoverticillactam, a 22-atom macrocyclic lactam incorporating both triene and tetraene conjugated olefins.

中文译文(包括题目)：
由海洋放线菌Streptomyces aureoverticillatus产生的22元环大环内酰胺Aureoverticillactam

在试图从海洋微生物中筛选得到新抗癌药物的过程中，我们发现一株分离自海洋沉积物的链酶菌属放线菌aureoverticillatus (NPS001583) 能产生一种新的大环内酰胺，其对数种不同的肿瘤细胞都有细胞毒作用。运用包括质谱、紫外及核磁共振的多种光谱分析，解析确定了该化合物1（aureoverticillactam）的结构，是一个含有共轭三烯和共轭四烯的22元环大环内酰胺。

如果你英语水平可以的话，可以直接到 （美国专利网）找找。

《外文文献信息检索》PPT版(包括：外文图书信息检索、外文期刊论文检索、外文报纸检索），如有需要再联系我。

张琚的主要学术论文

:张立国、石建党、冯剑利、李钟、张琚. Type IV collagenase (matrix metalloproteinase-2 and-9) in prostate cancer. PROSTATE CANCER AND PROSTATIC DISEASES 7-4-327.2005-1-1吴荃，周颖，陈林峰，石建党，王春雨，苗琳，Mocker, H; Park, I;李钟，张琚. Benign prostatic hyperplasia (BPH) epithelial cell line BPH-1 induces aromatase expression in prostatic stromal cells via prostaglandin E2. JOURNAL OF ENDOCRINOLOGY王春雨，石建党，闫春和，吴荃，Klocker, H; Park, I;李钟，张琚. Development of a cell-isolation method for human prostatic smooth muscle cells based on cell type-specific activation of the SM22 gene promoter. BJU INTERNATIONALZhang, J; Qi, HX; Wang, HJ; Hu, P; Ou, LL; Guo, SH; Li, J; Che, YZ;Yu,YT; Kong, DL. Engineering of vascular grafts with genetically modified bone marrow mesenchymal stem cells on poly (propylene carbonate) graft. ARTIFICIAL ORGANS张智松王亮梅玫朱彦杜小玲李钟Irwin Park张琚石建党. Both nongenomic and genomic effects are involved in estradiol’s enhancing the phenotype of smooth muscle cells in cultured prostate stromal cells. The Prostate樊官伟高秀梅王宏朱彦张琚胡黎明Yan-Fang Su, Li-Yuan Kang,张伯礼. The anti-inflammatory activities of Tanshinone IIA, an active component of TCM, are mediated by estr. Journal of Steroid Biochemistry & Molecular Biology周颖肖向茜陈林锋杨睿石建党杜小玲Helmut Klocker, Irwin Park李钟张琚. Proliferation and phenotypic changes of stromal cells in response to varying estrogen/androgen levels in castrated rats. Asian Journal of AndrologyIrwin I Park, Qiang Zhang, Victoria Liu,张琚, Chung Lee. Estrogen at low concentrations acts through distinct pathways in normal versus BPH-derived prostate stromal cells. the Journal of Clinical Endocrinology张立国王春雨杨睿石建党符蓉陈林锋Helmut Klocker张琚. Real-time quantitative RT-PCR assay of prostate-specific antigen and prostate-specific membrane antigen in peripheral blood for detection of prostate cancer micrometastasis. Urol Oncol张智松段磊杜小玲马洪顺Irwin Park李钟张琚石建党. The proliferative effect of estradiol on human prostate stromal cells is mediated through activation of ERK. The Prostate吴荃石建党陈林锋王春雨Irwin Park李钟张琚. Regulation of proliferation and differentiation of prostatic stromal cells by estradiol through prostateic epithelial cells (BPH-1) in a paracrine manner. The BJU International刘树业Yu XD, Song CJ, Lu W, Zhang JD, Shi XR, Duan Y张琚. Cloning and expression of special F protein from human liver. World Journal of Gastroenterology牛远杰马腾骧张琚徐勇韩瑞发孙光. Androgen and prostatic stroma. ChinaAsian J AndrolZhou W, Park I, Pins M, Kozlowski JM, Jovanovic B,张琚,李钟, Ilio K. Dual regulation of proliferation and growth arrest in prostatic stromal cells by transforming growth factor-beta1. Endocrinology张琚Klaus Jung, Michael Lein, Glen Kristiansen, Birgit Rudolph, Steffen Hauptmann, Dietmar Schnorr, Stefan A. Loening, and Ralf Lichtenhagen. Differential expression of matrix metalloproteinases and their tissue inhibitors in human primary cultured prostatic cells and malignant prostate cell lines. The Prostate牛远杰徐勇张琚马腾骧. Proliferation and differentiation of prostatic stromal cells. BJU InternationalSimone T. Boesch, Stefan Corvin,张琚, Hermann Rogatsch, George Bartsch, and Helmut Klocker. Modulation of the Differentiation Status of Cultured Prostatic Smooth Muscle Cells by an a1-Adrenergic Receptor Antagonist. The ProstateFibroblast Growth Factor Levels in Cancer Cell and in Sera of Patients suffering from Proliferative Disorders of the Prostate. The Prostate 31--223-233.1997-1-1张琚, Michael W. Hess, Martin Thurnher, Alfred Hobisch, Christian Radmayr, Marcus V. Cronauer, Anton Hittmair, Zoran Culig, Georg Bartsch and Helmut Klocker. Human prostatic smooth muscle Cell in culture: Estradiol enhances expression of smooth muscle cell-specific markers. The prostateZoran culig, Alfred hobisch, Marcus V. Cronauer, Christian Radmayr, Anton Hittmair,张琚, Martin Thurnher, Georg Bartsch and Helmut Klocker. Regulation of prostatic growth and function by peptide growth factors. The prostateMathias ziegler, Dierk Jorcke,张琚, Rainer Schneider, Helmut Klocker, Bernhard Auer, Manfred Schweiger. Characterization of Detergent-Solubilized Beef Liver Mitochodrial NAD?glycohydrolase and its Truncated Hydrosoluble Form. Biochemistry 35-16-5207-12.1996-4-23张琚, Mathias Ziegler, Rainer Schneider, Helmut Klocker, Bernhard Auer, Manfred Schweiger. identification and purification of a bovine liver mitochondrial NAD?glycohydrolase. FEBS LETTERS杨睿，张立国，符蓉，王春雨，刘树业，石建党，张琚. 实时定量PCR技术检测前列腺癌微小转移的研究. 南开大学学报于林，王春雨，杨睿，王亮，石建党*，张琚. TAT-GFP-ERB融合蛋白的原核表达与鉴定. 南开大学学报周颖,杨睿,石建党*,刘杰,杜小玲,王克明,张琚*. BPH间质细胞增殖和表型转化与雌激素受体α表达的关系. 解剖学报苗琳,石建党*,周颖,杜小玲,吴荃,王克明,张琚*. BPH-1通过分泌PGE2上调前列腺间质细胞ERR?的表达. 中国生物化学与分子生物学报张智松,刘杰,杜小玲,段磊,张琚*,石建党. 雌激素快速激活MAPK途径促进前列腺间质细胞的增殖. 中国生物化学与分子生物学报Rui Yang, Yu-Xia Ma, Lin-Feng Chen, Ying Zhou1, Zhan-Po Yang, Yan Zhu, Xiao-Ling Du, Jian-Dang Shi*, Hong-Shun Ma, Ju Zhang*. Antagonism of estrogen-mediated cell proliferation by raloxifene in prevention of ageing-related prostatic hyperplasia. Asian Journal of Andrology苗琳;周颖;石建党;杜小玲;焦鸿丽;张琚. 雌二醇通过TGFβ1促进前列腺间质细胞MMP-2的表达. 中国生物化学与分子生物学报 25-8-712-718.2009-8-1Lin Miao, Jiandang Shi , Chun-Yu Wang, Yan Zhu, Xiaoling Du, Hongli Jiao, Zengnan Mo, Helmut Klocker, Chung Lee, . Estrogen receptor-related receptor alpha mediates up-regulation of aromatase expression by prostaglandin E2 in prostate stromal cells. Mol EndocrinolRui Yang, Da Xu, Jiandang Shi*, Helmut Klocker, Chung Lee, Ju Zhang*. Tanshinone IIA inhibits estrogen/androgen induced prostatic stromal hyperplasia. The Journal of Urology --.Lin Yu, Jiandang Shi, Chun Yu Wang, Helmut klocker, Doris Mayer*, Ju Zhang*. Estradiol promotes the invasive potency of prostate cancer cells in a paracrine manner through stimulation of prostatic stromal cells. The Journal of Urology --.Z.S. Zhang, L. Wang, H.S. Ma, X.L. Du, J. Zhang*, J.D. Shi* . nongenomic and genomic effects are involved in estradiol’s enhancing the phenotype of smooth muscle cells in cultured prostate stromal cells(AUA). The Journal of Urology --.2009-5-28Y. Zhou, X.Q. Xiao, R. Yang, J.D. Shi*, X.L. Du, J. Zhang*. Dynamic changes of stromal cell in the process of estrogen/androgen induced prostatic stromal hyperplasia in castrated rats. The Journal of Urology --.2009-5-28贾金铭;马卫国;焦拥政;王家辉;罗少波;张琚;张智松. 癃必消胶囊对体外培养的人前列腺增生间质细胞作用机制的实验研究. 中国中西医结合杂志刘树业;杜智;商国强;贾艳慧;段缨;宋佐莉;张琚.. 肝癌中C53的表达及临床病理表现初探. 分子诊断与治疗杂志 1-2-104-107.2009-7-1马卫国;贾金铭;焦拥政;王家辉;罗少波;张琚;石建党;张智松. 癃必消胶囊对体外培养的人前列腺增生间质细胞Fibronectin和Collagen IV基因表达的影响. 中国男科学杂志马卫国;贾金铭;焦拥政;王家辉;罗少波;张琚;石建党;张智松. 癃必消胶囊对体外培养的人前列腺增生间质细胞TGF-β1和Smoothelin基因表达的影响. 中华男科学杂志袁庆东;肖向茜;梁承;张琚;赵建国. 电针用于治疗大鼠实验性前列腺增生症的机制研究. 中国康复医学杂志 23-6-532-534.2008-6-1樊官伟;王虹;张琚;高秀梅. 植物雌激素的临床价值. 国外医药（植物药分册）Iris ,Stefan Corvin,Christoph Maneschg,Marcus er,Georg Bartsch Jr,Ju Zhang,Arnulf Stenzl,Georg Bartsch,Helmut Klocker.. 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BMC Gastroenterology 11--1-10.2011-2-2彭雁飞，师莹，王亮，石建党*，杨小丽，张琚*. 用腺病毒载体包装不同分化程度平滑肌细胞特异性启动子的策略分离鉴定人前列腺间质细胞亚群. 南开大学学报Lin Yu, Jiandang Shi, Sa Cheng, Yan Zhu, Xiulan Zhao, Kuo Yang, Xiaoling Du,Helmut klocker，Xiaoli Yang，Ju Zhang*. Estrogen promotes prostate cancer cell migration via paracrine release of ENO1 from stromal cells. Molecular Endocrinology杜小玲，宁召臣，王春雨，石建党，张琚*. 类固醇激素受体辅助调节因子ARA55和TGFβ1在前列腺癌细胞中作用分子机制的研究. 南开大学学报（自然科学版）Lin Miao, Sina Grebhardt, Jiandang Shi, Isabelle Peipe, Ju Zhang, Doris Mayer. Prostaglandin E2 stimulates S100A8 expression by activating protein kinaseA and CCAAT/enhancer-binding-protein-beta in prostate cancer cells . The International Journal of Biochemistry & Cell Biology --1