Your browser doesn't support javascript.
loading
Nanoways to overcome docetaxel resistance in prostate cancer.
Ganju, Aditya; Yallapu, Murali M; Khan, Sheema; Behrman, Stephen W; Chauhan, Subhash C; Jaggi, Meena.
Affiliation
  • Ganju A; Department of Pharmaceutical Sciences and the Center for Cancer Research, College of Pharmacy, University of Tennessee Health Science Center, Memphis, TN 38163, USA; College of Graduate Health Sciences, University of Tennessee Health Science Center, Memphis, TN 38163, USA.
  • Yallapu MM; Department of Pharmaceutical Sciences and the Center for Cancer Research, College of Pharmacy, University of Tennessee Health Science Center, Memphis, TN 38163, USA. Electronic address: myallapu@uthsc.edu.
  • Khan S; Department of Pharmaceutical Sciences and the Center for Cancer Research, College of Pharmacy, University of Tennessee Health Science Center, Memphis, TN 38163, USA.
  • Behrman SW; Department of Surgery, University of Tennessee Health Science Center, Memphis, TN 38163, USA.
  • Chauhan SC; Department of Pharmaceutical Sciences and the Center for Cancer Research, College of Pharmacy, University of Tennessee Health Science Center, Memphis, TN 38163, USA. Electronic address: schauha1@uthsc.edu.
  • Jaggi M; Department of Pharmaceutical Sciences and the Center for Cancer Research, College of Pharmacy, University of Tennessee Health Science Center, Memphis, TN 38163, USA. Electronic address: mjaggi@uthsc.edu.
Drug Resist Updat ; 17(1-2): 13-23, 2014 Apr.
Article in En | MEDLINE | ID: mdl-24853766
ABSTRACT
Prostate cancer is the most common non-cutaneous malignancy in American men. Docetaxel is a useful chemotherapeutic agent for prostate cancer that has been available for over a decade, but the length of the treatment and systemic side effects hamper compliance. Additionally, docetaxel resistance invariably emerges, leading to disease relapse. Docetaxel resistance is either intrinsic or acquired by adopting various mechanisms that are highly associated with genetic alterations, decreased influx and increased efflux of drugs. Several combination therapies and small P-glycoprotein inhibitors have been proposed to improve the therapeutic potential of docetaxel in prostate cancer. Novel therapeutic strategies that may allow reversal of docetaxel resistance include alterations of enzymes, improving drug uptake and enhancement of apoptosis. In this review, we provide the most current docetaxel reversal approaches utilizing nanotechnology. Nanotechnology mediated docetaxel delivery is superior to existing therapeutic strategies and a more effective method to induce P-glycoprotein inhibition, enhance cellular uptake, maintain sustained drug release, and improve bioavailability.
Subject(s)
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Prostatic Neoplasms / Gene Expression Regulation, Neoplastic / Drug Resistance, Neoplasm / Taxoids / Nanoparticles / Neoplasm Recurrence, Local / Antineoplastic Agents Limits: Animals / Humans / Male Language: En Journal: Drug Resist Updat Journal subject: ANTINEOPLASICOS Year: 2014 Type: Article Affiliation country: United States

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Prostatic Neoplasms / Gene Expression Regulation, Neoplastic / Drug Resistance, Neoplasm / Taxoids / Nanoparticles / Neoplasm Recurrence, Local / Antineoplastic Agents Limits: Animals / Humans / Male Language: En Journal: Drug Resist Updat Journal subject: ANTINEOPLASICOS Year: 2014 Type: Article Affiliation country: United States