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New Advances of Macrophages in Cancer

A special issue of International Journal of Molecular Sciences (ISSN 1422-0067). This special issue belongs to the section "Molecular Biology".

Deadline for manuscript submissions: closed (30 November 2021) | Viewed by 12908

Special Issue Editors


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Guest Editor
Institute of General Pathology and Pathophysiology, Moscow State University of Medicine and Dentistry, Baltijskaya Street 8, 125315 Moscow, Russia
Interests: immunotherapy; biotechnology; adoptive cell transfer; macrophages; ex vivo cell reprogramming; solid tumour; ex vivo tumour models

E-Mail Website
Guest Editor
Institute of General Pathology and Pathophysiology, Moscow State University of Medicine and Dentistry, Baltijskaya Street 8, Moscow 125315, Russia
Interests: immunotherapy; biotechnology; adoptive cell transfer; macrophages; ex vivo cell reprogramming; solid tumour; ex vivo tumour models

Special Issue Information

Dear Colleagues,

Macrophages are a major component of the solid tumor microenvironment. Depending on their activation status, macrophages can exert dual influences on tumorigenesis, by either promoting tumor growth or by enhancing antitumor responses. Currently, there are two main macrophage-centered anticancer therapeutic strategies, namely: (1) depletion/re-education of disease-promoting tumor-associated macrophages (TAM), and (2) adoptive transfer of designer macrophages reprogrammed/engineered ex vivo and possessing anti-tumor activities. While TAM-targeting therapy has already yielded promising results in both preclinical and clinical trials, adoptive macrophage transfer is a relatively new paradigm. There is a strong hope that designer macrophages will finally deliver on the promise of adoptive cell immunotherapy for solid tumors. Indeed, the problem with the adoptive transfer of T cells and other lymphocytes is that they cannot easily reach the solid tumor microenvironment and persist once there. In contrast, macrophages and other phagocytes naturally traffic to tumors. This makes them “the perfect cell” type to reprogram for tumor-targeting purposes. This Special Issue will be dedicated to the current knowledge available on the pathophysiological role of macrophages in cancer and macrophage-centered approaches to anticancer therapy, including experimental tumor models. We welcome contributions in the form of original research articles and reviews.

Dr. Larisa Kuznetsova
Prof. Dr. Igor Malyshev
Guest Editors

Manuscript Submission Information

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Keywords

  • solid tumors
  • tumor microenvironment
  • macrophages
  • immunotherapy
  • TAM targeting
  • adoptive cell transfer
  • ex vivo macrophage reprogramming

Published Papers (3 papers)

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Research

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24 pages, 3946 KiB  
Article
Targeting Glycolysis in Macrophages Confers Protection Against Pancreatic Ductal Adenocarcinoma
by Hweixian Leong Penny, Je Lin Sieow, Sin Yee Gun, Mai Chan Lau, Bernett Lee, Jasmine Tan, Cindy Phua, Florida Toh, Yvonne Nga, Wei Hseun Yeap, Baptiste Janela, Dilip Kumar, Hao Chen, Joe Yeong, Justin A. Kenkel, Angela Pang, Diana Lim, Han Chong Toh, Tony Lim Kiat Hon, Christopher I. Johnson, Hanif Javanmard Khameneh, Alessandra Mortellaro, Edgar G. Engleman, Olaf Rotzschke, Florent Ginhoux, Jean-Pierre Abastado, Jinmiao Chen and Siew Cheng Wongadd Show full author list remove Hide full author list
Int. J. Mol. Sci. 2021, 22(12), 6350; https://0-doi-org.brum.beds.ac.uk/10.3390/ijms22126350 - 14 Jun 2021
Cited by 16 | Viewed by 4627
Abstract
Inflammation in the tumor microenvironment has been shown to promote disease progression in pancreatic ductal adenocarcinoma (PDAC); however, the role of macrophage metabolism in promoting inflammation is unclear. Using an orthotopic mouse model of PDAC, we demonstrate that macrophages from tumor-bearing mice exhibit [...] Read more.
Inflammation in the tumor microenvironment has been shown to promote disease progression in pancreatic ductal adenocarcinoma (PDAC); however, the role of macrophage metabolism in promoting inflammation is unclear. Using an orthotopic mouse model of PDAC, we demonstrate that macrophages from tumor-bearing mice exhibit elevated glycolysis. Macrophage-specific deletion of Glucose Transporter 1 (GLUT1) significantly reduced tumor burden, which was accompanied by increased Natural Killer and CD8+ T cell activity and suppression of the NLRP3-IL1β inflammasome axis. Administration of mice with a GLUT1-specific inhibitor reduced tumor burden, comparable with gemcitabine, the current standard-of-care. In addition, we observe that intra-tumoral macrophages from human PDAC patients exhibit a pronounced glycolytic signature, which reliably predicts poor survival. Our data support a key role for macrophage metabolism in tumor immunity, which could be exploited to improve patient outcomes. Full article
(This article belongs to the Special Issue New Advances of Macrophages in Cancer)
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Review

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16 pages, 273 KiB  
Review
Endometriosis and Cancer: Exploring the Role of Macrophages
by Daria Artemova, Polina Vishnyakova, Elena Khashchenko, Andrey Elchaninov, Gennady Sukhikh and Timur Fatkhudinov
Int. J. Mol. Sci. 2021, 22(10), 5196; https://0-doi-org.brum.beds.ac.uk/10.3390/ijms22105196 - 14 May 2021
Cited by 15 | Viewed by 3530
Abstract
Endometriosis and cancer have much in common, notably their burgeoning of cells in hypoxic milieus, their invasiveness, and their capacity to trigger remodeling, vascularization, and innervation of other tissues. An important role in these processes is played by permissive microenvironments inhabited by a [...] Read more.
Endometriosis and cancer have much in common, notably their burgeoning of cells in hypoxic milieus, their invasiveness, and their capacity to trigger remodeling, vascularization, and innervation of other tissues. An important role in these processes is played by permissive microenvironments inhabited by a variety of stromal and immune cells, including macrophages. Remarkable phenotypical plasticity of macrophages makes them a promising therapeutic target; some key issues are the range of macrophage phenotypes characteristic of a particular pathology and the possible manners of its modulation. In both endometriosis and cancer, macrophages guard the lesions from immune surveillance while promoting pathological cell growth, invasion, and metastasis. This review article focuses on a comparative analysis of macrophage behaviors in endometriosis and cancer. We also highlight recent reports on the experimental modulation of macrophage phenotypes in preclinical models of endometriosis and cancer. Full article
(This article belongs to the Special Issue New Advances of Macrophages in Cancer)
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26 pages, 2225 KiB  
Review
How Macrophages Become Transcriptionally Dysregulated: A Hidden Impact of Antitumor Therapy
by Galina F. Medvedeva, Daria O. Kuzmina, Julia Nuzhina, Alexander A. Shtil and Marina S. Dukhinova
Int. J. Mol. Sci. 2021, 22(5), 2662; https://0-doi-org.brum.beds.ac.uk/10.3390/ijms22052662 - 06 Mar 2021
Cited by 11 | Viewed by 4161
Abstract
Tumor-associated macrophages (TAMs) are the essential components of the tumor microenvironment. TAMs originate from blood monocytes and undergo pro- or anti-inflammatory polarization during their life span within the tumor. The balance between macrophage functional populations and the efficacy of their antitumor activities rely [...] Read more.
Tumor-associated macrophages (TAMs) are the essential components of the tumor microenvironment. TAMs originate from blood monocytes and undergo pro- or anti-inflammatory polarization during their life span within the tumor. The balance between macrophage functional populations and the efficacy of their antitumor activities rely on the transcription factors such as STAT1, NF-κB, IRF, and others. These molecular tools are of primary importance, as they contribute to the tumor adaptations and resistance to radio- and chemotherapy and can become important biomarkers for theranostics. Herein, we describe the major transcriptional mechanisms specific for TAM, as well as how radio- and chemotherapy can impact gene transcription and functionality of macrophages, and what are the consequences of the TAM-tumor cooperation. Full article
(This article belongs to the Special Issue New Advances of Macrophages in Cancer)
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