Literature DB >> 17414516

Novel targets and approaches in advanced prostate cancer.

Boris A Hadaschik1, Richard D Sowery, Martin E Gleave.   

Abstract

PURPOSE OF REVIEW: The development of therapeutic resistance is the underlying cause for most cancer deaths. By understanding the molecular basis of resistance to androgen withdrawal and chemotherapy in prostate cancer, the rational design of targeted therapeutics is possible. We review new treatment options for men with advanced prostate cancer. RECENT
FINDINGS: Although the taxanes currently represent the most active chemotherapeutic agents and standard of care for first-line treatment of metastatic hormone-refractory prostate cancer, most patients eventually progress because of intrinsic or acquired drug resistance. In recent years, increased knowledge of cancer progression and therapeutic resistance has identified many gene targets that regulate apoptosis, proliferation, and cell signalling. To date, numerous novel compounds have entered clinical trials as either single agents or in combination with cytotoxic chemotherapy.
SUMMARY: Even though hormone-refractory prostate cancer is still incurable, it is not untreatable. As cancer cells are proficient at adapting to therapeutic stressors, a combination regimen with drugs that target crucial cellular networks like the apoptotic rheostat may be more promising than treatment with highly selective single-target agents. Recent findings are very hopeful, but challenges remain to demonstrate effective antitumour activity in phase III trials with survival as the principal endpoint.

Entities:  

Mesh:

Substances:

Year:  2007        PMID: 17414516     DOI: 10.1097/MOU.0b013e3280dd8a4f

Source DB:  PubMed          Journal:  Curr Opin Urol        ISSN: 0963-0643            Impact factor:   2.309


  11 in total

1.  Induction of clusterin by AKT--role in cytoprotection against docetaxel in prostate tumor cells.

Authors:  Bin Zhong; David A Sallman; Danielle L Gilvary; Daniele Pernazza; Eva Sahakian; Dillon Fritz; Jin Q Cheng; Ioannis Trougakos; Sheng Wei; Julie Y Djeu
Journal:  Mol Cancer Ther       Date:  2010-05-25       Impact factor: 6.261

2.  [Optimizing treatment of advanced urologic malignancies].

Authors:  A Heidenreich; C H Ohlmann; E Ozgür; D Pfister; D Sahi; D Thüer; U H Engelmann
Journal:  Urologe A       Date:  2007-09       Impact factor: 0.639

3.  F10 Inhibits Growth of PC3 Xenografts and Enhances the Effects of Radiation Therapy.

Authors:  William H Gmeiner; Mark C Willingham; J Daniel Bourland; Heather C Hatcher; Thomas L Smith; Ralph B D'Agostino; William Blackstock
Journal:  J Clin Oncol Res       Date:  2014 Jul-Aug

4.  Acacetin inhibits VEGF expression, tumor angiogenesis and growth through AKT/HIF-1α pathway.

Authors:  Ling-Zhi Liu; Yi Jing; Lisa L Jiang; Xiu-E Jiang; Yue Jiang; Yongyut Rojanasakul; Bing-Hua Jiang
Journal:  Biochem Biophys Res Commun       Date:  2011-08-27       Impact factor: 3.575

5.  Selection and identification of ligand peptides targeting a model of castrate-resistant osteogenic prostate cancer and their receptors.

Authors:  Jami Mandelin; Marina Cardó-Vila; Wouter H P Driessen; Paul Mathew; Nora M Navone; Sue-Hwa Lin; Christopher J Logothetis; Anna Cecilia Rietz; Andrey S Dobroff; Bettina Proneth; Richard L Sidman; Renata Pasqualini; Wadih Arap
Journal:  Proc Natl Acad Sci U S A       Date:  2015-03-11       Impact factor: 11.205

6.  Molecular decoy to the Y-box binding protein-1 suppresses the growth of breast and prostate cancer cells whilst sparing normal cell viability.

Authors:  Jennifer H Law; Yvonne Li; Karen To; Michelle Wang; Arezoo Astanehe; Karen Lambie; Jaspreet Dhillon; Steven J M Jones; Martin E Gleave; Connie J Eaves; Sandra E Dunn
Journal:  PLoS One       Date:  2010-09-10       Impact factor: 3.240

7.  Clusterin, a haploinsufficient tumor suppressor gene in neuroblastomas.

Authors:  Olesya Chayka; Daisy Corvetta; Michael Dews; Alessandro E Caccamo; Izabela Piotrowska; Giorgia Santilli; Sian Gibson; Neil J Sebire; Nourredine Himoudi; Michael D Hogarty; John Anderson; Saverio Bettuzzi; Andrei Thomas-Tikhonenko; Arturo Sala
Journal:  J Natl Cancer Inst       Date:  2009-04-28       Impact factor: 13.506

8.  RHAMM (CD168) is overexpressed at the protein level and may constitute an immunogenic antigen in advanced prostate cancer disease.

Authors:  Kilian M Gust; Matthias D Hofer; Sven R Perner; Robert Kim; Arul M Chinnaiyan; Sooryanarayana Varambally; Peter Moller; Ludwig Rinnab; Mark A Rubin; Jochen Greiner; Michael Schmitt; Rainer Kuefer; Mark Ringhoffer
Journal:  Neoplasia       Date:  2009-09       Impact factor: 5.715

9.  Downregulation of miR-205 and miR-31 confers resistance to chemotherapy-induced apoptosis in prostate cancer cells.

Authors:  N Bhatnagar; X Li; S K R Padi; Q Zhang; M-S Tang; B Guo
Journal:  Cell Death Dis       Date:  2010-12-09       Impact factor: 8.469

Review 10.  Human xenograft models as useful tools to assess the potential of novel therapeutics in prostate cancer.

Authors:  W M van Weerden; C Bangma; R de Wit
Journal:  Br J Cancer       Date:  2008-12-16       Impact factor: 7.640

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.