Literature DB >> 33352766

Natural and Synthetic PPARγ Ligands in Tumor Microenvironment: A New Potential Strategy against Breast Cancer.

Giuseppina Augimeri1,2, Luca Gelsomino1, Pierluigi Plastina1, Cinzia Giordano1,3, Ines Barone1,3, Stefania Catalano1,3, Sebastiano Andò1,3, Daniela Bonofiglio1,3.   

Abstract

Multiple lines of evidence indicate that activation of the peroxisome proliferator-activated receptor γ (PPARγ) by natural or synthetic ligands exerts tumor suppressive effects in different types of cancer, including breast carcinoma. Over the past decades a new picture of breast cancer as a complex disease consisting of neoplastic epithelial cells and surrounding stroma named the tumor microenvironment (TME) has emerged. Indeed, TME is now recognized as a pivotal element for breast cancer development and progression. Novel strategies targeting both epithelial and stromal components are under development or undergoing clinical trials. In this context, the aim of the present review is to summarize PPARγ activity in breast TME focusing on the role of this receptor on both epithelial/stromal cells and extracellular matrix components of the breast cancer microenvironment. The information provided from the in vitro and in vivo research indicates PPARγ ligands as potential agents with regards to the battle against breast cancer.

Entities:  

Keywords:  PPARγ ligands; breast cancer; cancer-associated adipocytes; cancer-associated fibroblasts; extracellular matrix components; extracellular vesicles; peroxisome proliferator-activated receptor gamma; tumor endothelial cells; tumor microenvironment; tumor-associated macrophages

Mesh:

Substances:

Year:  2020        PMID: 33352766      PMCID: PMC7767156          DOI: 10.3390/ijms21249721

Source DB:  PubMed          Journal:  Int J Mol Sci        ISSN: 1422-0067            Impact factor:   5.923


  111 in total

Review 1.  Macrophage diversity enhances tumor progression and metastasis.

Authors:  Bin-Zhi Qian; Jeffrey W Pollard
Journal:  Cell       Date:  2010-04-02       Impact factor: 41.582

Review 2.  Mechanistic insights of adipocyte metabolism in regulating breast cancer progression.

Authors:  Fuchuang Zhang; Suling Liu
Journal:  Pharmacol Res       Date:  2020-03-06       Impact factor: 7.658

3.  New Approaches to Cancer Therapy: Combining Fatty Acid Amide Hydrolase (FAAH) Inhibition with Peroxisome Proliferator-Activated Receptors (PPARs) Activation.

Authors:  Leonardo Brunetti; Fulvio Loiodice; Luca Piemontese; Paolo Tortorella; Antonio Laghezza
Journal:  J Med Chem       Date:  2019-08-22       Impact factor: 7.446

4.  PPAR gamma represses VEGF expression in human endometrial cells: implications for uterine angiogenesis.

Authors:  Louis L H Peeters; Jean-Louis Vigne; Meng Kian Tee; Dong Zhao; Leslie L Waite; Robert N Taylor
Journal:  Angiogenesis       Date:  2006-01-07       Impact factor: 9.596

5.  Bifunctional properties of peroxisome proliferator-activated receptor gamma1 in KDR gene regulation mediated via interaction with both Sp1 and Sp3.

Authors:  Yukio Sassa; Yasuaki Hata; Lloyd Paul Aiello; Yukio Taniguchi; Kimitoshi Kohno; Tatsuro Ishibashi
Journal:  Diabetes       Date:  2004-05       Impact factor: 9.461

6.  Ligand-activated PPARγ downregulates CXCR4 gene expression through a novel identified PPAR response element and inhibits breast cancer progression.

Authors:  Daniela Rovito; Giulia Gionfriddo; Ines Barone; Cinzia Giordano; Fedora Grande; Francesca De Amicis; Marilena Lanzino; Stefania Catalano; Sebastiano Andò; Daniela Bonofiglio
Journal:  Oncotarget       Date:  2016-10-04

Review 7.  Role of extracellular matrix in breast cancer development: a brief update.

Authors:  Manoj Kumar Jena; Jagadeesh Janjanam
Journal:  F1000Res       Date:  2018-03-05

8.  Activation of β2-Adrenergic Receptor Promotes Growth and Angiogenesis in Breast Cancer by Down-regulating PPARγ.

Authors:  Jing Zhou; Zhanzhao Liu; Lingjing Zhang; Xiao Hu; Zhihua Wang; Hong Ni; Yue Wang; Junfang Qin
Journal:  Cancer Res Treat       Date:  2020-03-04       Impact factor: 4.679

9.  IL-6-mediated cross-talk between human preadipocytes and ductal carcinoma in situ in breast cancer progression.

Authors:  Hoe Suk Kim; Minji Jung; Sul Ki Choi; Jisu Woo; Yin Ji Piao; Eun Hye Hwang; Hyelim Kim; Seung Ja Kim; Woo Kyung Moon
Journal:  J Exp Clin Cancer Res       Date:  2018-08-22

10.  Caspase-1 cleaves PPARγ for potentiating the pro-tumor action of TAMs.

Authors:  Zhiyuan Niu; Qian Shi; Wenlong Zhang; Yuxin Shu; Nanfei Yang; Bing Chen; Qingsong Wang; Xuyang Zhao; Jiajia Chen; Nan Cheng; Xiujing Feng; Zichun Hua; Jianguo Ji; Pingping Shen
Journal:  Nat Commun       Date:  2017-10-03       Impact factor: 14.919

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  3 in total

1.  CircRNA TGFBR2/MiR-25-3p/TWIST1 axis regulates osteoblast differentiation of human aortic valve interstitial cells.

Authors:  Cheng Yu; Dannan Wu; Chong Zhao; Chaoguang Wu
Journal:  J Bone Miner Metab       Date:  2020-10-18       Impact factor: 2.626

2.  Ligand-activated PPARδ expression promotes hepatocellular carcinoma progression by regulating the PI3K-AKT signaling pathway.

Authors:  Wei Han; Nan Wang; Rui Kong; Wen Bao; Jie Lu
Journal:  J Transl Med       Date:  2022-02-12       Impact factor: 5.531

3.  PPARgamma: A Potential Intrinsic and Extrinsic Molecular Target for Breast Cancer Therapy.

Authors:  Giuseppina Augimeri; Daniela Bonofiglio
Journal:  Biomedicines       Date:  2021-05-13
  3 in total

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