Literature DB >> 36107314

Nuclear Receptors and Lipid Sensing.

James L Thorne1, Giorgia Cioccoloni2.   

Abstract

Fluctuations in concentration of diverse lipid classes occur in response to diet and metabolism. These changes are managed and mediated by a cell network of enzymes, pumps, and carriers under the control of the lipid responsive nuclear receptors. The understanding of how dysregulation of lipid metabolism are causes and indicators of disease beyond the cardiovascular system has developed in the last decade. A particular emphasis on the role of lipids and lipid-sensing nuclear receptors has emerged in the fields of cancer and the immune system's interaction with cancer. The range of known lipid-based ligands has also expanded. Lipids are not just signalling molecules, but also play structural roles in cells and tissues, for example as major constituents of the lipid bilayer - positioning them as integrators and mediators of signaling. This chapter will discuss the major groups of lipid-sensing nuclear receptors focusing on the liver x receptors, farnesoid x receptor, and the peroxisome proliferator-activated receptors. Initially the reader is presented with information on how these receptors behave and function at the molecular biology level, the range of selective modulation of function by endogenous ligands, and examples of how activity is fine-tuned by mechanisms such as miRNA regulation and post-translational modification of the proteins. We then explore the advances in understanding that have positioned these receptors as therapeutic targets in cancer and immuno-oncology. Finally, the chapter explains the gaps in understanding and experimental challenges that should be prioritized in the coming decade.
© 2022. The Author(s), under exclusive license to Springer Nature Switzerland AG.

Entities:  

Keywords:  Cancer; Immuno-oncology; Lipids; Oxysterols; Selective modulation; Splicing; Transcription

Mesh:

Substances:

Year:  2022        PMID: 36107314     DOI: 10.1007/978-3-031-11836-4_5

Source DB:  PubMed          Journal:  Adv Exp Med Biol        ISSN: 0065-2598            Impact factor:   3.650


  200 in total

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Authors:  M Adams; M J Reginato; D Shao; M A Lazar; V K Chatterjee
Journal:  J Biol Chem       Date:  1997-02-21       Impact factor: 5.157

Review 2.  Alternative Splicing in the Nuclear Receptor Superfamily Expands Gene Function to Refine Endo-Xenobiotic Metabolism.

Authors:  Andrew J Annalora; Craig B Marcus; Patrick L Iversen
Journal:  Drug Metab Dispos       Date:  2020-01-24       Impact factor: 3.922

3.  SUMOylation of the farnesoid X receptor (FXR) regulates the expression of FXR target genes.

Authors:  Natarajan Balasubramaniyan; Yuhuan Luo; An-Qiang Sun; Frederick J Suchy
Journal:  J Biol Chem       Date:  2013-04-01       Impact factor: 5.157

4.  Activation of Farnesoid X Receptor impairs the tumor-promoting function of breast cancer-associated fibroblasts.

Authors:  Ines Barone; Valentina Vircillo; Cinzia Giordano; Luca Gelsomino; Balázs Győrffy; Roberta Tarallo; Antonio Rinaldi; Giuseppina Bruno; Antonella Caruso; Francesco Romeo; Daniela Bonofiglio; Sebastiano Andò; Stefania Catalano
Journal:  Cancer Lett       Date:  2018-09-01       Impact factor: 8.679

5.  Elevated NCOR1 disrupts PPARalpha/gamma signaling in prostate cancer and forms a targetable epigenetic lesion.

Authors:  Sebastiano Battaglia; Orla Maguire; James L Thorne; Laura B Hornung; Craig L Doig; Song Liu; Lara E Sucheston; Anna Bianchi; Farhat L Khanim; Lyndon M Gommersall; Henry S O Coulter; Serena Rakha; Ian Giddings; Laura P O'Neill; Colin S Cooper; Christopher J McCabe; Christopher M Bunce; Moray J Campbell
Journal:  Carcinogenesis       Date:  2010-05-13       Impact factor: 4.944

6.  Elevated NCOR1 disrupts a network of dietary-sensing nuclear receptors in bladder cancer cells.

Authors:  S Asad Abedin; James L Thorne; Sebastiano Battaglia; Orla Maguire; Laura B Hornung; Alan P Doherty; Ian G Mills; Moray J Campbell
Journal:  Carcinogenesis       Date:  2009-01-06       Impact factor: 4.944

7.  Low density lipoprotein (LDL) cholesterol is converted to 27-hydroxycholesterol in human fibroblasts. Evidence that 27-hydroxycholesterol can be an important intracellular mediator between LDL and the suppression of cholesterol production.

Authors:  M Axelson; O Larsson
Journal:  J Biol Chem       Date:  1995-06-23       Impact factor: 5.157

8.  PGC-1α Promotes Breast Cancer Metastasis and Confers Bioenergetic Flexibility against Metabolic Drugs.

Authors:  Sylvia Andrzejewski; Eva Klimcakova; Radia M Johnson; Sébastien Tabariès; Matthew G Annis; Shawn McGuirk; Jason J Northey; Valérie Chénard; Urshila Sriram; David J Papadopoli; Peter M Siegel; Julie St-Pierre
Journal:  Cell Metab       Date:  2017-10-05       Impact factor: 27.287

9.  Activation of the Farnesoid X-receptor in breast cancer cell lines results in cytotoxicity but not increased migration potential.

Authors:  Noura Alasmael; Rati Mohan; Lisiane B Meira; Karen E Swales; Nick J Plant
Journal:  Cancer Lett       Date:  2015-11-03       Impact factor: 8.679

10.  The cholesterol metabolite 27 hydroxycholesterol facilitates breast cancer metastasis through its actions on immune cells.

Authors:  Amy E Baek; Yen-Rei A Yu; Sisi He; Suzanne E Wardell; Ching-Yi Chang; Sanghoon Kwon; Ruchita V Pillai; Hannah B McDowell; J Will Thompson; Laura G Dubois; Patrick M Sullivan; Jongsook K Kemper; Michael D Gunn; Donald P McDonnell; Erik R Nelson
Journal:  Nat Commun       Date:  2017-10-11       Impact factor: 14.919

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