| Literature DB >> 33297362 |
Malvina Marku1,2, Nina Verstraete1,2, Flavien Raynal1,2, Miguel Madrid-Mencía1,2, Marcin Domagala1,2, Jean-Jacques Fournié1,2, Loïc Ysebaert1,2,3, Mary Poupot1,2, Vera Pancaldi1,2,4.
Abstract
The tumour microenvironment is the surrounding of a tumour, including blood vessels, fibroblasts, signaling molecules, the extracellular matrix and immune cells, especially neutrophils and monocyte-derived macrophages. In a tumour setting, macrophages encompass a spectrum between a tumour-suppressive (M1) or tumour-promoting (M2) state. The biology of macrophages found in tumours (Tumour Associated Macrophages) remains unclear, but understanding their impact on tumour progression is highly important. In this paper, we perform a comprehensive analysis of a macrophage polarization network, following two lines of enquiry: (i) we reconstruct the macrophage polarization network based on literature, extending it to include important stimuli in a tumour setting, and (ii) we build a dynamical model able to reproduce macrophage polarization in the presence of different stimuli, including the contact with cancer cells. Our simulations recapitulate the documented macrophage phenotypes and their dependencies on specific receptors and transcription factors, while also unravelling the formation of a special type of tumour associated macrophages in an in vitro model of chronic lymphocytic leukaemia. This model constitutes the first step towards elucidating the cross-talk between immune and cancer cells inside tumours, with the ultimate goal of identifying new therapeutic targets that could control the formation of tumour associated macrophages in patients.Entities:
Keywords: Boolean model; chronic lymphocytic leukaemia; macrophage polarization; nurse-like cells; tumour associated macrophage
Year: 2020 PMID: 33297362 PMCID: PMC7762229 DOI: 10.3390/cancers12123664
Source DB: PubMed Journal: Cancers (Basel) ISSN: 2072-6694 Impact factor: 6.639