TY - JOUR
T1 - Emerging molecular mechanisms and genetic targets for developing novel therapeutic strategies for treating bladder diseases
AU - Zoqlam, Randa
AU - Lazauskaite, Sandra
AU - Glickman, Scott
AU - Zaitseva, Lyubov
AU - Ilie, Petre-Cristian
AU - Qi, Sheng
N1 - Funding Information: This study was supported by a UKRI Medical Research Council Doctoral Antimicrobial Research Training (DART) PhD CASE Studentship Award [grant number MR/R015937/1] and the University of East Anglia, in collaboration with UroPharma Ltd.
PY - 2022/6/1
Y1 - 2022/6/1
N2 - Bladder diseases affect millions of patients worldwide and compromise their quality of life with a substantial economic impact. The not fully understood aetiologies of bladder diseases limit the current diagnosis and therapeutic options to primarily symptomatic treatment. In addition, bladder targeted drug delivery is challenging due to its unique anatomical features and its natural physiological function of urine storage and frequent voiding. Therefore, current treatment options often fail to provide a highly effective, precisely targeted and long-lasting treatment. With the growing maturity of gene therapy, comprehensive studies are needed to provide a better understanding of the molecular mechanisms underpinning bladder diseases and help to identify novel gene therapeutic targets and biomarkers for treating bladder diseases. In this review, molecular mechanisms involved in pathology of bladder cancer, interstitial cystitis and overactive bladder syndrome are reviewed, with focus on establishing potential novel treatment options. Proposed novel therapies, including gene therapy combined with nanotechnology, localised drug delivery by nanoparticles, and probiotics, are discussed in regard to their safety profiles, efficacy, treatment lenght, precise targeting, and in comparison to conventional treatment methods.
AB - Bladder diseases affect millions of patients worldwide and compromise their quality of life with a substantial economic impact. The not fully understood aetiologies of bladder diseases limit the current diagnosis and therapeutic options to primarily symptomatic treatment. In addition, bladder targeted drug delivery is challenging due to its unique anatomical features and its natural physiological function of urine storage and frequent voiding. Therefore, current treatment options often fail to provide a highly effective, precisely targeted and long-lasting treatment. With the growing maturity of gene therapy, comprehensive studies are needed to provide a better understanding of the molecular mechanisms underpinning bladder diseases and help to identify novel gene therapeutic targets and biomarkers for treating bladder diseases. In this review, molecular mechanisms involved in pathology of bladder cancer, interstitial cystitis and overactive bladder syndrome are reviewed, with focus on establishing potential novel treatment options. Proposed novel therapies, including gene therapy combined with nanotechnology, localised drug delivery by nanoparticles, and probiotics, are discussed in regard to their safety profiles, efficacy, treatment lenght, precise targeting, and in comparison to conventional treatment methods.
KW - Bladder cancer
KW - Gene therapy
KW - Interstitial cystitis, Nanoparticles
KW - Overactive bladder
KW - Probiotics
UR - http://www.scopus.com/inward/record.url?scp=85126580655&partnerID=8YFLogxK
U2 - 10.1016/j.ejps.2022.106167
DO - 10.1016/j.ejps.2022.106167
M3 - Article
VL - 173
JO - European Journal of Pharmaceutical Sciences
JF - European Journal of Pharmaceutical Sciences
SN - 0928-0987
M1 - 106167
ER -