Literature DB >> 28073818

Transcriptional coregulator RIP140: an essential regulator of physiology.

Jaya Nautiyal1.   

Abstract

Transcriptional coregulators drive gene regulatory decisions in the transcriptional space. Although transcription factors including all nuclear receptors provide a docking platform for coregulators to bind, these proteins bring enzymatic capabilities to the gene regulatory sites. RIP140 is a transcriptional coregulator essential for several physiological processes, and aberrations in its function may lead to diseased states. Unlike several other coregulators that are known either for their coactivating or corepressing roles, in gene regulation, RIP140 is capable of acting both as a coactivator and a corepressor. The role of RIP140 in female reproductive axis and recent findings of its role in carcinogenesis and adipose biology have been summarised.
© 2017 Society for Endocrinology.

Entities:  

Keywords:  RIP140; adipose; cancer; coregulators; inflammation; mammary gland; metabolism; obesity; ovulation

Mesh:

Substances:

Year:  2017        PMID: 28073818     DOI: 10.1530/JME-16-0156

Source DB:  PubMed          Journal:  J Mol Endocrinol        ISSN: 0952-5041            Impact factor:   5.098


  6 in total

1.  The Transcription Coregulator RIP140 Inhibits Cancer Cell Proliferation by Targeting the Pentose Phosphate Pathway.

Authors:  Valentin Jacquier; Delphine Gitenay; Vincent Cavaillès; Catherine Teyssier
Journal:  Int J Mol Sci       Date:  2022-07-04       Impact factor: 6.208

Review 2.  Contribution of PGC-1α to Obesity- and Caloric Restriction-Related Physiological Changes in White Adipose Tissue.

Authors:  Masaki Kobayashi; Yusuke Deguchi; Yuka Nozaki; Yoshikazu Higami
Journal:  Int J Mol Sci       Date:  2021-06-02       Impact factor: 5.923

3.  FLT1 and transcriptome-wide polyadenylation site (PAS) analysis in preeclampsia.

Authors:  Ami Ashar-Patel; Yasin Kaymaz; Augustine Rajakumar; Jeffrey A Bailey; S Ananth Karumanchi; Melissa J Moore
Journal:  Sci Rep       Date:  2017-09-22       Impact factor: 4.379

4.  NRIP1 is activated by C-JUN/C-FOS and activates the expression of PGR, ESR1 and CCND1 in luminal A breast cancer.

Authors:  Renata Binato; Stephany Corrêa; Carolina Panis; Gerson Ferreira; Igor Petrone; Igor Rodrigues da Costa; Eliana Abdelhay
Journal:  Sci Rep       Date:  2021-10-27       Impact factor: 4.379

5.  RIP140 inhibits glycolysis-dependent proliferation of breast cancer cells by regulating GLUT3 expression through transcriptional crosstalk between hypoxia induced factor and p53.

Authors:  Vincent Cavaillès; Catherine Teyssier; Valentin Jacquier; Delphine Gitenay; Samuel Fritsch; Sandrine Bonnet; Balázs Győrffy; Stéphan Jalaguier; Laetitia K Linares
Journal:  Cell Mol Life Sci       Date:  2022-05-03       Impact factor: 9.207

6.  Differential in Vitro Biological Action, Coregulator Interactions, and Molecular Dynamic Analysis of Bisphenol A (BPA), BPAF, and BPS Ligand-ERα Complexes.

Authors:  Yin Li; Lalith Perera; Laurel A Coons; Katherine A Burns; J Tyler Ramsey; Katherine E Pelch; René Houtman; Rinie van Beuningen; Christina T Teng; Kenneth S Korach
Journal:  Environ Health Perspect       Date:  2018-01-31       Impact factor: 9.031

  6 in total

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