Chemokines and NSCLC: Emerging role in prognosis, heterogeneity, and therapeutics.
Chemokines
Prognostic markers
Therapeutics
Tumor microenvironment
Journal
Seminars in cancer biology
ISSN: 1096-3650
Titre abrégé: Semin Cancer Biol
Pays: England
ID NLM: 9010218
Informations de publication
Date de publication:
11 2022
11 2022
Historique:
received:
02
02
2022
revised:
15
06
2022
accepted:
24
06
2022
pubmed:
6
7
2022
medline:
18
11
2022
entrez:
5
7
2022
Statut:
ppublish
Résumé
Lung cancer persists to contribute to one-quarter of cancer-associated deaths. Among the different histologies, non-small cell lung cancer (NSCLC) alone accounts for 85% of the cases. The development of therapies involving immune checkpoint inhibitors and angiogenesis inhibitors has increased patients' survival probability and reduced mortality rates. Developing targeted therapies against essential genetic alterations also translates to better treatment strategies. But the benefits still seem farfetched due to the development of drug resistance and refractory tumors. In this review, we have highlighted the interplay of different tumor microenvironment components, essentially discussing the chemokine families (CC, CXC, C, and CX3C) that regulate the tumor biology in NSCLC and promote tumor growth, metastasis, and associated heterogeneity. The development of therapeutics and prognostic markers is a complex and multipronged approach. However, some essential chemokines can act as critical players for being considered potential prognostic markers and therapeutic targets.
Identifiants
pubmed: 35787939
pii: S1044-579X(22)00154-7
doi: 10.1016/j.semcancer.2022.06.010
pii:
doi:
Substances chimiques
Chemokines
0
Types de publication
Journal Article
Review
Research Support, U.S. Gov't, Non-P.H.S.
Langues
eng
Sous-ensembles de citation
IM
Pagination
233-246Informations de copyright
Copyright © 2022. Published by Elsevier Ltd.
Déclaration de conflit d'intérêts
Conflicts of interest The authors have no conflicts of interest to disclose.