Literature DB >> 12771527

Multidrug resistance in prostate cancer.

J P van Brussel1, G H J Mickisch.   

Abstract

Advanced hormone-refractory prostate cancer remains a therapeutic challenge, because all available pharmaceutical concepts have been ineffective in improving cancer-specific survival. Failure of chemotherapy may be caused by multidrug resistance (MDR) mechanisms protecting cancer cells against cytotoxic drugs, and the question arises whether prostate cancer is also using MDR principles resulting in resistance against chemotherapeutic agents. In consequence, an array of diverse pathways known to lead to MDR such as MDR1, MRPs, glutathione, and apoptosis have been examined and partially established at varying degrees in hormone-refractory prostate cancer. Thus, evidence keeps accumulating for the involvement of some MDR mechanisms in the chemoresistance of prostate cancer in vitro and in vivo. For some of them, e.g. MRP1, functional expression appears to be probable. This lends credit to the idea that reversal, circumvention, or overcoming of MDR pathways in advanced prostate cancer may be feasible and will lead to new avenues with improved treatment efficacy in otherwise intractable disease. Copyright 2003 S. Karger GmbH, Freiburg

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Year:  2003        PMID: 12771527     DOI: 10.1159/000071510

Source DB:  PubMed          Journal:  Onkologie        ISSN: 0378-584X


  22 in total

1.  Frequency of brain metastases from prostate cancer: an 18-year single-institution experience.

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Journal:  J Neurooncol       Date:  2012-10-25       Impact factor: 4.130

2.  Paclitaxel- and lapatinib-loaded lipopolymer micelles overcome multidrug resistance in prostate cancer.

Authors:  Feng Li; Michael Danquah; Saurabh Singh; Hao Wu; Ram I Mahato
Journal:  Drug Deliv Transl Res       Date:  2011-12       Impact factor: 4.617

3.  Liver protects metastatic prostate cancer from induced death by activating E-cadherin signaling.

Authors:  Bo Ma; Sarah E Wheeler; Amanda M Clark; Diana L Whaley; Min Yang; Alan Wells
Journal:  Hepatology       Date:  2016-09-23       Impact factor: 17.425

Review 4.  Portrait of multifaceted transporter, the multidrug resistance-associated protein 1 (MRP1/ABCC1).

Authors:  Eva Bakos; László Homolya
Journal:  Pflugers Arch       Date:  2006-12-23       Impact factor: 3.657

5.  The NRF2-mediated oxidative stress response pathway is associated with tumor cell resistance to arsenic trioxide across the NCI-60 panel.

Authors:  Qian Liu; Hao Zhang; Lisa Smeester; Fei Zou; Matt Kesic; Ilona Jaspers; Jingbo Pi; Rebecca C Fry
Journal:  BMC Med Genomics       Date:  2010-08-13       Impact factor: 3.063

Review 6.  Functions of normal and malignant prostatic stem/progenitor cells in tissue regeneration and cancer progression and novel targeting therapies.

Authors:  Murielle Mimeault; Parmender P Mehta; Ralph Hauke; Surinder K Batra
Journal:  Endocr Rev       Date:  2008-02-21       Impact factor: 19.871

Review 7.  MicroRNAs and drug resistance in prostate cancers.

Authors:  Feng Li; Ram I Mahato
Journal:  Mol Pharm       Date:  2014-04-29       Impact factor: 4.939

Review 8.  Targeting prostate cancer based on signal transduction and cell cycle pathways.

Authors:  John T Lee; Brian D Lehmann; David M Terrian; William H Chappell; Franca Stivala; Massimo Libra; Alberto M Martelli; Linda S Steelman; James A McCubrey
Journal:  Cell Cycle       Date:  2008-06-16       Impact factor: 4.534

9.  Pharmacologic inhibition of Pim kinases alters prostate cancer cell growth and resensitizes chemoresistant cells to taxanes.

Authors:  Shannon M Mumenthaler; Patricia Y B Ng; Amanda Hodge; David Bearss; Gregory Berk; Sarath Kanekal; Sanjeev Redkar; Pietro Taverna; David B Agus; Anjali Jain
Journal:  Mol Cancer Ther       Date:  2009-10       Impact factor: 6.261

10.  Tumor cell-selective apoptosis induction through targeting of K(V)10.1 via bifunctional TRAIL antibody.

Authors:  Franziska Hartung; Walter Stühmer; Luis A Pardo
Journal:  Mol Cancer       Date:  2011-09-07       Impact factor: 27.401

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