A detailed insight into macrophages' role in shaping lung carcinogenesis.

Alveolar macrophages Inflammation Macrophage plasticity Nrf2 Tumour microenvironment

Journal

Life sciences
ISSN: 1879-0631
Titre abrégé: Life Sci
Pays: Netherlands
ID NLM: 0375521

Informations de publication

Date de publication:
05 Jul 2024
Historique:
received: 05 03 2024
revised: 24 06 2024
accepted: 03 07 2024
medline: 8 7 2024
pubmed: 8 7 2024
entrez: 7 7 2024
Statut: aheadofprint

Résumé

Despite significant advancements in cancer treatment in recent decades, the high mortality rate associated with lung cancer remains a significant concern. The development and proper execution of new targeted therapies needs more deep knowledge regarding the lung cancer associated tumour microenvironment. One of the key component of that tumour microenvironment is the lung resident macrophages. Although in normal physiological condition the lung resident macrophages are believed to maintain lung homeostasis, but they may also initiate a vicious inflammatory response in abnormal conditions which is linked to lung cancer development. Depending on the activation pathway, the lung resident macrophages are either of M1 or M2 sub-type. The M1 and M2 sub-types differ significantly in various prospectuses, from phenotypic markers to metabolic pathways. In addition to this generalized classification, the recent advancement of the multiomics technology is able to identify some other sub-types of lung resident macrophages. Researchers have also observed that these different sub-types can manipulate the pathogenesis of lung carcinogenesis in a context dependent manner and can either promote or inhibit the development of lung carcinogenesis upon receiving proper activation. As proper knowledge about the role played by the lung resident macrophages' in shaping the lung carcinogenesis is limited so the main purpose of this review is to bring all the available information under the same roof. We also elaborated the different mechanisms involved in maintenance of the plasticity of M1/M2 sub-type as this plasticity can be a good target for lung cancer treatment.

Identifiants

pubmed: 38972632
pii: S0024-3205(24)00486-7
doi: 10.1016/j.lfs.2024.122896
pii:
doi:

Types de publication

Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

122896

Informations de copyright

Copyright © 2024. Published by Elsevier Inc.

Déclaration de conflit d'intérêts

Declaration of competing interest Authors declare that there is no conflict of interest.

Auteurs

Tamanna Aktar (T)

Immunology Microbiology Lab, Tripura University, Suryamaninagar, Tripura 799022, India.

Snehashish Modak (S)

Immunology Microbiology Lab, Tripura University, Suryamaninagar, Tripura 799022, India.

Debabrata Majumder (D)

Immunology Microbiology Lab, Tripura University, Suryamaninagar, Tripura 799022, India; Department of Integrative Immunobiology, Duke University Medical Center, Durham, NC 27710, USA.

Debasish Maiti (D)

Immunology Microbiology Lab, Tripura University, Suryamaninagar, Tripura 799022, India. Electronic address: debasish.maiti@tripurauniv.in.

Classifications MeSH