Literature DB >> 28695226

Fenretinide differentially modulates the levels of long- and very long-chain ceramides by downregulating Cers5 enzyme: evidence from bench to bedside.

Dušan Garić1, Juan B De Sanctis2, Gabriella Wojewodka1,3, Daniel Houle4, Shanon Cupri4, Asmahan Abu-Arish5, John W Hanrahan5, Marian Hajduch6, Elias Matouk4, Danuta Radzioch7,8.   

Abstract

Cystic fibrosis is the most common genetic disease, in which symptoms may be alleviated but not fully eliminated. Ceramides have long been implicated in the inflammatory etiology of cystic fibrosis, with contradicting reports with regards to their role. Recently, significant biological and biophysical differences have been observed between long- and very long-chain ceramides. This work reveals that long-chain ceramides are upregulated whereas very long-chain ceramides are downregulated in cell lines, mouse animal model, and patients with cystic fibrosis, compared with their controls. Treatment with fenretinide decreases the levels of long-chain ceramides and increases the levels of very long-chain ceramides. Our results show that restoration of cystic fibrosis conductance regulator (CFTR) expression is associated with normalization of aberrant levels of specific ceramides. This demonstrates for the first time a correlation between CFTR protein expression and regulation of specific ceramide levels. Furthermore, using cystic fibrosis lung epithelial cell lines, we demonstrate that this effect can be attributed to the transcriptional downregulation of ceramide synthase 5 (Cers5) enzyme. We also discovered a partial synergism between fenretinide and zinc (Zn2+), which deficiency has been reported in patients with cystic fibrosis. Overall, in addition to having direct translational application, we believe that our findings contribute to the understanding of ceramide metabolism in cystic fibrosis, as well as other inflammatory diseases where imbalances of ceramides have also been observed. KEY MESSAGES: Long- and very long-chain ceramides (LCCs and VLCCs) are biochemically distinct. LCCs are upregulated whereas VLCCs are downregulated in cystic fibrosis. Fenretinide downregulates the levels of LCCs and upregulates the levels of VLCCs. Fenretinide changes the balance of LCCs and VLCCs by downregulating Cers5 enzyme. Fenretinide and zinc ions cooperate in the modulation of ceramide levels.

Entities:  

Keywords:  Ceramides; Cystic fibrosis; Fenretinide

Mesh:

Substances:

Year:  2017        PMID: 28695226     DOI: 10.1007/s00109-017-1564-y

Source DB:  PubMed          Journal:  J Mol Med (Berl)        ISSN: 0946-2716            Impact factor:   4.599


  44 in total

Review 1.  Cystic fibrosis genetics: from molecular understanding to clinical application.

Authors:  Garry R Cutting
Journal:  Nat Rev Genet       Date:  2014-11-18       Impact factor: 53.242

2.  PPAR activation and decreased proliferation in oral carcinoma cells with 4-HPR.

Authors:  George Harris; Raed Abu Ghazallah; David Nascene; Beverly Wuertz; Frank G Ondrey
Journal:  Otolaryngol Head Neck Surg       Date:  2005-11       Impact factor: 3.497

Review 3.  Translating the genetics of cystic fibrosis to personalized medicine.

Authors:  Harriet Corvol; Kristin E Thompson; Olivier Tabary; Philippe le Rouzic; Loïc Guillot
Journal:  Transl Res       Date:  2015-04-15       Impact factor: 7.012

4.  Long chain ceramides and very long chain ceramides have opposite effects on human breast and colon cancer cell growth.

Authors:  Daniela Hartmann; Jessica Lucks; Sina Fuchs; Susanne Schiffmann; Yannick Schreiber; Nerea Ferreirós; Jennifer Merkens; Rolf Marschalek; Gerd Geisslinger; Sabine Grösch
Journal:  Int J Biochem Cell Biol       Date:  2012-01-02       Impact factor: 5.085

5.  Zinc modulates PPARgamma signaling and activation of porcine endothelial cells.

Authors:  Purushothaman Meerarani; Gudrun Reiterer; Michal Toborek; Bernhard Hennig
Journal:  J Nutr       Date:  2003-10       Impact factor: 4.798

6.  Cystic fibrosis fatty acid imbalance is linked to ceramide deficiency and corrected by fenretinide.

Authors:  Claudine Guilbault; Gabriella Wojewodka; Zienab Saeed; Marian Hajduch; Elias Matouk; Juan B De Sanctis; Danuta Radzioch
Journal:  Am J Respir Cell Mol Biol       Date:  2008-12-04       Impact factor: 6.914

7.  Effect of zinc supplementation on respiratory tract infections in children with cystic fibrosis.

Authors:  I Abdulhamid; F W J Beck; S Millard; X Chen; A Prasad
Journal:  Pediatr Pulmonol       Date:  2008-03

8.  Decreased expression of peroxisome proliferator activated receptor gamma in cftr-/- mice.

Authors:  Mario Ollero; Omer Junaidi; Munir M Zaman; Iphigenia Tzameli; Adolfo A Ferrando; Charlotte Andersson; Paola G Blanco; Eldad Bialecki; Steven D Freedman
Journal:  J Cell Physiol       Date:  2004-08       Impact factor: 6.384

9.  Fenretinide corrects newly found ceramide deficiency in cystic fibrosis.

Authors:  Claudine Guilbault; Juan B De Sanctis; Gabriella Wojewodka; Zienab Saeed; Claude Lachance; Thomas A A Skinner; Regina M Vilela; Stan Kubow; Larry C Lands; Marian Hajduch; Elias Matouk; Danuta Radzioch
Journal:  Am J Respir Cell Mol Biol       Date:  2007-07-26       Impact factor: 6.914

10.  Host defense against Pseudomonas aeruginosa requires ceramide-rich membrane rafts.

Authors:  H Grassmé; V Jendrossek; A Riehle; G von Kürthy; J Berger; H Schwarz; M Weller; R Kolesnick; E Gulbins
Journal:  Nat Med       Date:  2003-02-03       Impact factor: 53.440

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  10 in total

1.  Cystic fibrosis: the conductance regulator, ceramides, and possible treatments.

Authors:  Friedrich C Luft
Journal:  J Mol Med (Berl)       Date:  2017-10       Impact factor: 4.599

2.  Efficacy of Optimized Treatment Protocol Using LAU-7b Formulation against Ovalbumin (OVA) and House Dust Mite (HDM) -Induced Allergic Asthma in Atopic Hyperresponsive A/J Mice.

Authors:  Mina Youssef; Juan B De Sanctis; Cynthia Kanagaratham; Shao Tao; Eisha Ahmed; Danuta Radzioch
Journal:  Pharm Res       Date:  2020-01-08       Impact factor: 4.200

3.  Airway profile of bioactive lipids predicts early progression of lung disease in cystic fibrosis.

Authors:  Hamed Horati; Hettie M Janssens; Camilla Margaroli; Mieke Veltman; Marta Stolarczyk; Matthew B Kilgore; Jeffrey Chou; Limin Peng; Harm A M W Tiddens; Joshua D Chandler; Rabindra Tirouvanziam; Bob J Scholte
Journal:  J Cyst Fibros       Date:  2020-02-10       Impact factor: 5.482

4.  Treatment With LAU-7b Complements CFTR Modulator Therapy by Improving Lung Physiology and Normalizing Lipid Imbalance Associated With CF Lung Disease.

Authors:  Amanda Centorame; Daciana Catalina Dumut; Mina Youssef; Martin Ondra; Irenej Kianicka; Juhi Shah; Radu Alexandru Paun; Tomas Ozdian; John W Hanrahan; Ekaterina Gusev; Basil Petrof; Marian Hajduch; Radu Pislariu; Juan Bautista De Sanctis; Danuta Radzioch
Journal:  Front Pharmacol       Date:  2022-05-20       Impact factor: 5.988

5.  Vitamin A and beta (β)-carotene supplementation for cystic fibrosis.

Authors:  Jorrit Jv de Vries; Anne B Chang; Catherine M Bonifant; Elizabeth Shevill; Julie M Marchant
Journal:  Cochrane Database Syst Rev       Date:  2018-08-09

6.  Agonists that stimulate secretion promote the recruitment of CFTR into membrane lipid microdomains.

Authors:  Asmahan Abu-Arish; Elvis Pandžić; Dusik Kim; Hsin Wei Tseng; Paul W Wiseman; John W Hanrahan
Journal:  J Gen Physiol       Date:  2019-05-02       Impact factor: 4.086

Review 7.  Proteostasis Regulators in Cystic Fibrosis: Current Development and Future Perspectives.

Authors:  Irene Brusa; Elvira Sondo; Federico Falchi; Nicoletta Pedemonte; Marinella Roberti; Andrea Cavalli
Journal:  J Med Chem       Date:  2022-04-04       Impact factor: 8.039

Review 8.  Proteomics and Metabolomics for Cystic Fibrosis Research.

Authors:  Nara Liessi; Nicoletta Pedemonte; Andrea Armirotti; Clarissa Braccia
Journal:  Int J Mol Sci       Date:  2020-07-30       Impact factor: 5.923

9.  Sphingomyelinase decreases transepithelial anion secretion in airway epithelial cells in part by inhibiting CFTR-mediated apical conductance.

Authors:  Kirsten A Cottrill; Raven J Peterson; Colby F Lewallen; Michael Koval; Robert J Bridges; Nael A McCarty
Journal:  Physiol Rep       Date:  2021-08

10.  Lipid-driven CFTR clustering is impaired in cystic fibrosis and restored by corrector drugs.

Authors:  Asmahan Abu-Arish; Elvis Pandžić; Yishan Luo; Yukiko Sato; Mark J Turner; Paul W Wiseman; John W Hanrahan
Journal:  J Cell Sci       Date:  2022-03-07       Impact factor: 5.285

  10 in total

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