Literature DB >> 17428163

Synthetic retinoid fenretinide in breast cancer chemoprevention.

Bernardo Bonanni1, Matteo Lazzeroni, Umberto Veronesi.   

Abstract

Preclinical models suggest that retinoids inhibit mammary carcinogenesis. The induction of apoptosis is a unique feature of fenretinide, the most-studied retinoid in clinical trials of breast cancer chemoprevention, owing to its selective accumulation in breast tissue and its favorable toxicological profile. In a Phase III breast cancer prevention trial, fenretinide showed a strong trend of reduction of incidence of second breast malignancies in premenopausal women, which was confirmed by 15 years of follow-up. This warrants further research on the mechanisms of action and potential efficacy of fenretinide and provides the rationale for a Phase III primary prevention trial in young women at high risk for breast cancer. This review will highlight the role of fenretinide in breast cancer chemoprevention.

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Year:  2007        PMID: 17428163     DOI: 10.1586/14737140.7.4.423

Source DB:  PubMed          Journal:  Expert Rev Anticancer Ther        ISSN: 1473-7140            Impact factor:   4.512


  8 in total

1.  Enhanced apoptotic cancer cell killing after Foscan photodynamic therapy combined with fenretinide via de novo sphingolipid biosynthesis pathway.

Authors:  Nithin B Boppana; Jeremy S DeLor; Eric Van Buren; Alicja Bielawska; Jacek Bielawski; Jason S Pierce; Mladen Korbelik; Duska Separovic
Journal:  J Photochem Photobiol B       Date:  2016-03-16       Impact factor: 6.252

2.  Sphingosine kinase mediates resistance to the synthetic retinoid N-(4-hydroxyphenyl)retinamide in human ovarian cancer cells.

Authors:  Giuditta Illuzzi; Caterina Bernacchioni; Massimo Aureli; Simona Prioni; Gianluca Frera; Chiara Donati; Manuela Valsecchi; Vanna Chigorno; Paola Bruni; Sandro Sonnino; Alessandro Prinetti
Journal:  J Biol Chem       Date:  2010-04-19       Impact factor: 5.157

3.  Sphingolipidomics of A2780 human ovarian carcinoma cells treated with synthetic retinoids.

Authors:  Manuela Valsecchi; Massimo Aureli; Laura Mauri; Giuditta Illuzzi; Vanna Chigorno; Alessandro Prinetti; Sandro Sonnino
Journal:  J Lipid Res       Date:  2010-03-01       Impact factor: 5.922

4.  Identification of dihydroceramide desaturase as a direct in vitro target for fenretinide.

Authors:  Mehrdad Rahmaniyan; Robert W Curley; Lina M Obeid; Yusuf A Hannun; Jacqueline M Kraveka
Journal:  J Biol Chem       Date:  2011-05-04       Impact factor: 5.157

5.  Fumonisin B1 Inhibits Endoplasmic Reticulum Stress Associated-apoptosis After FoscanPDT Combined with C6-Pyridinium Ceramide or Fenretinide.

Authors:  Nithin B Boppana; Jacqueline M Kraveka; Mehrdad Rahmaniyan; L I Li; Alicja Bielawska; Jacek Bielawski; Jason S Pierce; Jeremy S Delor; Kezhong Zhang; Mladen Korbelik; Duska Separovic
Journal:  Anticancer Res       Date:  2017-02       Impact factor: 2.480

6.  In vitro activities of novel 4-HPR derivatives on a panel of rhabdoid and other tumor cell lines.

Authors:  Melissa E Smith; Bhaskar C Das; Ganjam V Kalpana
Journal:  Cancer Cell Int       Date:  2011-09-27       Impact factor: 5.722

7.  Sustained, local delivery of the PARP inhibitor talazoparib prevents the development of mammary gland hyperplasia in Brca1-deficient mice.

Authors:  Di Zhang; Bijay Singh; Jessica Moerland; Owen Mitchell; Lizbeth Lockwood; Sarah Carapellucci; Srinivas Sridhar; Karen T Liby
Journal:  Sci Rep       Date:  2021-01-13       Impact factor: 4.379

8.  Fenretinide (4-HPR) Targets Caspase-9, ERK 1/2 and the Wnt3a/β-Catenin Pathway in Medulloblastoma Cells and Medulloblastoma Cell Spheroids.

Authors:  Barbara Bassani; Desirèe Bartolini; Arianna Pagani; Elisa Principi; Massimo Zollo; Douglas M Noonan; Adriana Albini; Antonino Bruno
Journal:  PLoS One       Date:  2016-07-01       Impact factor: 3.240

  8 in total

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