Overexpression of CXCR4 synergizes with LL-37 in the metastasis of breast cancer cells-Reference-Cited by-同舟云学术

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Overexpression of CXCR4 synergizes with LL-37 in the metastasis of breast cancer cells

Published:2018-11 Issue:11 Volume:1864 Page:3837-3846
ISSN:0925-4439
Container-title:Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease
language:en
Short-container-title:Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease

Author:

Pan Wen Liang,Wang Yan,Hao Yuan,Wong Jack Ho,Chan Wing Cheong,Wan David Chi-Cheong,Ng Tzi Bun

Funder

Health and Medical Research Fund

Food and Health Bureau

National Natural Science Foundation of China

Publisher

Elsevier BV

Subject

Molecular Biology,Molecular Medicine

Reference48 articles.

1. Global cancer statistics;Jemal;CA Cancer J. Clin.,2011

2. Global patterns of cancer incidence and mortality rates and trends;Jemal;Cancer Epidemiol. Biomark. Prev.,2010

3. Ligand-activated PPARgamma downregulates CXCR4 gene expression through a novel identified PPAR response element and inhibits breast cancer progression;Rovito;Oncotarget,2016

4. Identification of novel 2-(1H-indol-1-yl)-benzohydrazides CXCR4 ligands impairing breast cancer growth and motility;Grande;Future Med. Chem.,2016

5. Involvement of chemokine receptors in breast cancer metastasis;Muller;Nature,2001

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2. Identifying and Assessing Putative Allosteric Sites and Modulators for CXCR4 Predicted through Network Modeling and Site Identification by Ligand Competitive Saturation;The Journal of Physical Chemistry B;2024-04-22

3. CXCL17 is an allosteric inhibitor of CXCR4 through a mechanism of action involving glycosaminoglycans;Science Signaling;2024-03-19

4. Cathelicidin LL-37 promotes EMT, migration and metastasis of hepatocellular carcinoma cells in vitro and mouse model;Cell Adhesion & Migration;2023-01-19

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