Immunomodulation via macrophages to fight solid tumor malignancies
- PMID: 32578301
- DOI: 10.1111/febs.15437
Immunomodulation via macrophages to fight solid tumor malignancies
Abstract
The paper 'A C-Terminal Fragment of Adhesion Protein Fibulin-7 Inhibits Growth of Murine Breast Tumor by Regulating Macrophage Reprogramming' by Chakraborty et al. highlights that Fbln7-C could be explored as a potential immunomodulatory agent against various solid cancers and have shown its abilities to regulate tumor microenvironment reprogramming of TAMs in a breast cancer model. Fbln7, which is a secreted glycoprotein, has been shown to be anti-angiogenic and has an immunomodulatory role regulating various functional properties of monocytes, macrophages, and neutrophils, thereby influencing inflammation. In this study, the authors have shown that in a murine breast tumor model, intravenous administration of Fbln7-C significantly reduces the size of tumors via macrophage reprogramming. Comment on: https://doi.org/10.1111/febs.15333.
Keywords: fibulins; immunomodulation; macrophages; solid tumor.
© 2020 Federation of European Biochemical Societies.
Comment on
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A C-terminal fragment of adhesion protein fibulin-7 inhibits growth of murine breast tumor by regulating macrophage reprogramming.FEBS J. 2021 Feb;288(3):803-817. doi: 10.1111/febs.15333. Epub 2020 May 1. FEBS J. 2021. PMID: 32297473
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- Chakraborty P, Dash SP, Dalpati N, Kumar P, Jain D & Sarangi PP (2020) A C-Terminal fragment of adhesion protein fibulin-7 inhibits growth of murine breast tumor by regulating macrophage reprogramming [published online ahead of print, 2020 Apr 16]. FEBS J 288, 803-817.
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