Literature DB >> 24597633

A new dawn for the use of thiazolidinediones in cancer therapy.

Hardik Joshi1, Tanushree Pal, C S Ramaa.   

Abstract

INTRODUCTION: The thiazolidinedione (TZD) class of PPAR-γ ligands is predominantly known for its insulin sensitization activity. Unfortunately, these drugs have discernible side effects at diabetic dose. However, rosiglitazone and pioglitazone are still in the market with controversies. Past few years have noted the use of these drugs for the treatment of various other ailments. AREAS COVERED: In this review, the authors present the anticancer mechanisms of established TZDs and highlight some of the new-fangled agents discovered. Remarkable preclinical and clinical activity of the known and newly developed agents, alone or in combination with the known cytotoxic agents, offer a new perspective for clinical studies carving a niche in cancer chemotherapy. EXPERT OPINION: Various preclinical and clinical studies strongly suggest a role for TZDs both alone and in combination with existing chemotherapeutic agents, for the treatment of cancer. The exploration of newer TZDs at different doses, as well as developing partial agonists, can potentially help in unveiling the underlying mechanisms of these therapeutics, and consequently, treat this dreadful group of diseases.

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Year:  2014        PMID: 24597633     DOI: 10.1517/13543784.2014.884708

Source DB:  PubMed          Journal:  Expert Opin Investig Drugs        ISSN: 1354-3784            Impact factor:   6.206


  12 in total

1.  Structure guided design and synthesis of furyl thiazolidinedione derivatives as inhibitors of GLUT 1 and GLUT 4, and evaluation of their anti-leukemic potential.

Authors:  Kalpana Tilekar; Neha Upadhyay; Jessica D Hess; Lucasantiago Henze Macias; Piotr Mrowka; Renato J Aguilera; Franz-Josef Meyer-Almes; Cristina V Iancu; Jun-Yong Choe; C S Ramaa
Journal:  Eur J Med Chem       Date:  2020-07-02       Impact factor: 6.514

2.  The Cannabidiol Analog PECS-101 Prevents Chemotherapy-Induced Neuropathic Pain via PPARγ Receptors.

Authors:  Nicole Rodrigues Silva; Francisco Isaac Fernandes Gomes; Alexandre Hashimoto Pereira Lopes; Isadora Lopes Cortez; Jéssica Cristina Dos Santos; Conceição Elidianne Aníbal Silva; Raphael Mechoulam; Felipe Villela Gomes; Thiago Mattar Cunha; Francisco Silveira Guimarães
Journal:  Neurotherapeutics       Date:  2021-12-13       Impact factor: 6.088

3.  Distinct gene regulatory programs define the inhibitory effects of liver X receptors and PPARG on cancer cell proliferation.

Authors:  Daniel Savic; Ryne C Ramaker; Brian S Roberts; Emma C Dean; Todd C Burwell; Sarah K Meadows; Sara J Cooper; Michael J Garabedian; Jason Gertz; Richard M Myers
Journal:  Genome Med       Date:  2016-07-11       Impact factor: 11.117

4.  Synthesis and Anticancer Activity of New 1-Thia-4-azaspiro[4.5]decane, Their Derived Thiazolopyrimidine and 1,3,4-Thiadiazole Thioglycosides.

Authors:  Eman M Flefel; Wael A El-Sayed; Ashraf M Mohamed; Walaa I El-Sofany; Hanem M Awad
Journal:  Molecules       Date:  2017-01-20       Impact factor: 4.411

5.  Design, Molecular Docking, Synthesis, Anticancer and Anti-Hyperglycemic Assessments of Thiazolidine-2,4-diones Bearing Sulfonylthiourea Moieties as Potent VEGFR-2 Inhibitors and PPARγ Agonists.

Authors:  Mohamed A Abdelgawad; Khaled El-Adl; Sanadelaslam S A El-Hddad; Mostafa M Elhady; Nashwa M Saleh; Mohamed M Khalifa; Fathalla Khedr; Mohamed Alswah; AbdElAziz A Nayl; Mohammed M Ghoneim; Nour E A Abd El-Sattar
Journal:  Pharmaceuticals (Basel)       Date:  2022-02-14

Review 6.  An update on PPAR activation by cannabinoids.

Authors:  Saoirse Elizabeth O'Sullivan
Journal:  Br J Pharmacol       Date:  2016-05-19       Impact factor: 8.739

7.  Oxaliplatin neurotoxicity involves peroxisome alterations. PPARγ agonism as preventive pharmacological approach.

Authors:  Matteo Zanardelli; Laura Micheli; Lorenzo Cinci; Paola Failli; Carla Ghelardini; Lorenzo Di Cesare Mannelli
Journal:  PLoS One       Date:  2014-07-18       Impact factor: 3.240

8.  Pioglitazone Effect on Glioma Stem Cell Lines: Really a Promising Drug Therapy for Glioblastoma?

Authors:  Chiara Cilibrasi; Valentina Butta; Gabriele Riva; Angela Bentivegna
Journal:  PPAR Res       Date:  2016-05-25       Impact factor: 4.964

9.  Peroxisome proliferator-activated receptor (PPAR) α and δ activators induce ICAM-1 expression in quiescent non stimulated endothelial cells.

Authors:  Julia Naidenow; Igor Hrgovic; Monika Doll; Tsige Hailemariam-Jahn; Victoria Lang; Johannes Kleemann; Stefan Kippenberger; Roland Kaufmann; Nadja Zöller; Markus Meissner
Journal:  J Inflamm (Lond)       Date:  2016-08-20       Impact factor: 4.981

10.  CB11, a novel purine-based PPARɣ ligand, overcomes radio-resistance by regulating ATM signalling and EMT in human non-small-cell lung cancer cells.

Authors:  Tae Woo Kim; Da-Won Hong; Joung Whan Park; Sung Hee Hong
Journal:  Br J Cancer       Date:  2020-09-22       Impact factor: 7.640

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