Literature DB >> 21252099

Potential use of HMG-CoA reductase inhibitors (statins) as radioprotective agents.

Gerhard Fritz1, Christian Henninger, Johannes Huelsenbeck.   

Abstract

HMG-CoA reductase inhibitors (statins) are widely used in the therapy of hypercholesterolemia. Apart from their lipid-lowering activity, they have pleiotropic effects that are attributed to the inhibition of regulatory proteins, including Ras-homologous (Rho) GTPases. Here, we discuss the potential usefulness of statins to prevent normal tissue damage provoked by radiotherapy. Statins reduce the mRNA expression of pro-inflammatory and pro-fibrotic cytokines stimulated by ionizing radiation in vitro and alleviate IR-induced inflammation and fibrosis in vivo. The currently available data indicate that statins accelerate the rapid repair of DNA double-strand breaks and, moreover, mitigate the DNA damage response induced by IR. Furthermore, statins increase the mRNA expression of DNA repair factors in vivo. Thus, although the molecular mechanisms involved are still ambiguous, preclinical data concordantly show a promising radioprotective capacity of statins.

Entities:  

Mesh:

Substances:

Year:  2011        PMID: 21252099     DOI: 10.1093/bmb/ldq044

Source DB:  PubMed          Journal:  Br Med Bull        ISSN: 0007-1420            Impact factor:   4.291


  20 in total

1.  Simvastatin improves hematopoietic stem cell engraftment by preventing irradiation-induced marrow adipogenesis and radio-protecting the niche cells.

Authors:  Manmohan S Bajaj; Suprita S Ghode; Rohan S Kulkarni; Lalita S Limaye; Vaijayanti P Kale
Journal:  Haematologica       Date:  2015-04-17       Impact factor: 9.941

2.  Strategies to optimize radiotherapy based on biological responses of tumor and normal tissue.

Authors:  Weidong Wang; Jinyi Lang
Journal:  Exp Ther Med       Date:  2012-05-30       Impact factor: 2.447

Review 3.  Functional response difference between diabetic/normal cancerous patients to inflammatory cytokines and oxidative stresses after radiotherapy.

Authors:  Parinaz Mehnati; Behzad Baradaran; Fatemeh Vahidian; Sousan Nadiriazam
Journal:  Rep Pract Oncol Radiother       Date:  2020-06-30

4.  HMG-CoA Reductase Inhibition Delays DNA Repair and Promotes Senescence After Tumor Irradiation.

Authors:  Elena V Efimova; Natalia Ricco; Edwardine Labay; Helena J Mauceri; Amy C Flor; Aishwarya Ramamurthy; Harold G Sutton; Ralph R Weichselbaum; Stephen J Kron
Journal:  Mol Cancer Ther       Date:  2017-10-13       Impact factor: 6.261

Review 5.  Therapeutic potential of natural plant products and their metabolites in preventing radiation enteropathy resulting from abdominal or pelvic irradiation.

Authors:  Rupak Pathak; Sumit K Shah; Martin Hauer-Jensen
Journal:  Int J Radiat Biol       Date:  2019-01-08       Impact factor: 2.694

Review 6.  Novel Indications for Commonly Used Medications as Radiation Protectants in Spaceflight.

Authors:  Mark F McLaughlin; Dorit B Donoviel; Jeffrey A Jones
Journal:  Aerosp Med Hum Perform       Date:  2017-07-01       Impact factor: 1.053

Review 7.  Addressing the Symptoms or Fixing the Problem? Developing Countermeasures against Normal Tissue Radiation Injury.

Authors:  Jacqueline P Williams; Laura Calvi; Joe V Chakkalakal; Jacob N Finkelstein; M Kerry O'Banion; Edward Puzas
Journal:  Radiat Res       Date:  2016-06-22       Impact factor: 2.841

8.  Differential effects of lovastatin on cisplatin responses in normal human mesothelial cells versus cancer cells: implication for therapy.

Authors:  Yandong Shi; Emanuela Felley-Bosco; Thomas M Marti; Rolf A Stahel
Journal:  PLoS One       Date:  2012-09-17       Impact factor: 3.240

Review 9.  Cancer Stem Cells and Radioresistance: Rho/ROCK Pathway Plea Attention.

Authors:  Annapurna Pranatharthi; Cecil Ross; Sweta Srivastava
Journal:  Stem Cells Int       Date:  2016-08-15       Impact factor: 5.443

10.  Rac1 modulates acute and subacute genotoxin-induced hepatic stress responses, fibrosis and liver aging.

Authors:  A Bopp; F Wartlick; C Henninger; B Kaina; G Fritz
Journal:  Cell Death Dis       Date:  2013-03-21       Impact factor: 8.469

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.