Literature DB >> 17826663

Therapeutic options for hormone-refractory prostate cancer in 2007.

Boris A Hadaschik1, Martin E Gleave.   

Abstract

Prostate cancer is the most commonly diagnosed cancer in American men and a major health problem. While localized disease has an excellent chance for cure, metastatic disease leads to androgen-independent progression and death within a few years. Although docetaxel represents an important therapeutic milestone and is the current standard of care for metastatic hormone-refractory prostate cancer (HRPC), most patients eventually progress because of clonal selection of therapy-resistant cells or the development of cells with a drug-resistant phenotype. By understanding the molecular basis of resistance to androgen withdrawal and chemotherapy, the rational design of targeted therapeutics is possible. Over the last few years, many gene targets that regulate apoptosis, proliferation, and cell signalling have been identified, and numerous novel compounds have entered clinical trials either as single agents or in combination with cytotoxic chemotherapy. Neoadjuvant trials in particular must be further encouraged since they allow detection of biological activity in the prostatectomy specimen. This article reviews new treatment options available for men with advanced prostate cancer. Even though HRPC remains incurable, it is not untreatable. Recent findings are very promising, but challenges remain in demonstrating effective anti-tumor activity and showing a clinically relevant survival benefit in Phase III trials.

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Year:  2007        PMID: 17826663     DOI: 10.1016/j.urolonc.2007.05.010

Source DB:  PubMed          Journal:  Urol Oncol        ISSN: 1078-1439            Impact factor:   3.498


  23 in total

1.  Silibinin inhibits established prostate tumor growth, progression, invasion, and metastasis and suppresses tumor angiogenesis and epithelial-mesenchymal transition in transgenic adenocarcinoma of the mouse prostate model mice.

Authors:  Rana P Singh; Komal Raina; Girish Sharma; Rajesh Agarwal
Journal:  Clin Cancer Res       Date:  2008-12-01       Impact factor: 12.531

2.  Exosomes secreted under hypoxia enhance invasiveness and stemness of prostate cancer cells by targeting adherens junction molecules.

Authors:  Anand Ramteke; Harold Ting; Chapla Agarwal; Samiha Mateen; Ranganathan Somasagara; Anowar Hussain; Michael Graner; Barbara Frederick; Rajesh Agarwal; Gagan Deep
Journal:  Mol Carcinog       Date:  2013-12-17       Impact factor: 4.784

3.  A phase I clinical study of high dose ketoconazole plus weekly docetaxel for metastatic castration resistant prostate cancer.

Authors:  William D Figg; Sukyung Woo; Wenhui Zhu; Xiaohong Chen; A Seun Ajiboye; Seth M Steinberg; Douglas K Price; John J Wright; Howard L Parnes; Philip M Arlen; James L Gulley; William L Dahut
Journal:  J Urol       Date:  2010-06       Impact factor: 7.450

4.  p21/Cip1 and p27/Kip1 Are essential molecular targets of inositol hexaphosphate for its antitumor efficacy against prostate cancer.

Authors:  Srirupa Roy; Mallikarjuna Gu; Kumaraguruparan Ramasamy; Rana P Singh; Chapla Agarwal; Sunitha Siriwardana; Robert A Sclafani; Rajesh Agarwal
Journal:  Cancer Res       Date:  2009-01-27       Impact factor: 12.701

5.  Expression of the Bcl-2 protein BAD promotes prostate cancer growth.

Authors:  Adrienne J Smith; Yelena Karpova; Ralph D'Agostino; Mark Willingham; George Kulik
Journal:  PLoS One       Date:  2009-07-13       Impact factor: 3.240

6.  NF-kappaB activation enhances cell death by antimitotic drugs in human prostate cancer cells.

Authors:  Ricardo Parrondo; Alicia de las Pozas; Teresita Reiner; Priyamvada Rai; Carlos Perez-Stable
Journal:  Mol Cancer       Date:  2010-07-09       Impact factor: 27.401

7.  CXC receptor-1 silencing inhibits androgen-independent prostate cancer.

Authors:  Nagarajarao Shamaladevi; Dominic A Lyn; Diogo O Escudero; Bal L Lokeshwar
Journal:  Cancer Res       Date:  2009-10-27       Impact factor: 12.701

Review 8.  Chemokines and chemokine receptors as promoters of prostate cancer growth and progression.

Authors:  Nicole Salazar; Miguel Castellan; Samir S Shirodkar; Bal L Lokeshwar
Journal:  Crit Rev Eukaryot Gene Expr       Date:  2013       Impact factor: 1.807

9.  Depletion of intrinsic expression of Interleukin-8 in prostate cancer cells causes cell cycle arrest, spontaneous apoptosis and increases the efficacy of chemotherapeutic drugs.

Authors:  Rajendra K Singh; Bal L Lokeshwar
Journal:  Mol Cancer       Date:  2009-07-31       Impact factor: 27.401

10.  Cyclin D1 repressor domain mediates proliferation and survival in prostate cancer.

Authors:  M J Schiewer; L M Morey; C J Burd; Y Liu; D E Merry; S-M Ho; K E Knudsen
Journal:  Oncogene       Date:  2008-12-15       Impact factor: 9.867

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