File Download

There are no files associated with this item.

  Links for fulltext
     (May Require Subscription)
Supplementary

Article: Chemical carcinogens: implications for cancer treatment

TitleChemical carcinogens: implications for cancer treatment
Authors
Issue Date16-Oct-2023
PublisherAmerican Society for Clinical Investigation
Citation
The Journal of Clinical Investigation, 2023, v. 133, n. 20 How to Cite?
AbstractCarcinogen exposure has been associated with enhanced cancer immunogenicity that is often attributed to neoantigen generation. However, the broader, neoantigen-independent impact of carcinogens on immune responses to cancer cells remains underexplored. In this issue of the JCI, Huang et al. uncover a mechanism wherein carcinogen-treated cancer cells exhibit an inability to establish an immunosuppressive tumor microenvironment (TME) due to reduced M-CSF expression. Intriguingly, the so-called carcinogen-induced tumor-associated macrophages (TAMs) within this TME exhibited anti-tumor properties instead of the conventional immunosuppressive phenotype. This phenomenon extended to human lung cancers, as evidenced by TAM reprogramming in smokers versus nonsmokers. This study substantially advances our understanding of carcinogen-mediated effects on cancer immunogenicity, potentially redirecting approaches to cancer immunotherapy.
Persistent Identifierhttp://hdl.handle.net/10722/346351
ISSN
2023 Impact Factor: 13.3
2023 SCImago Journal Rankings: 4.833

 

DC FieldValueLanguage
dc.contributor.authorLiu, Shaofeng-
dc.contributor.authorSaunders, Mary-
dc.contributor.authorMak, Tak Wah-
dc.date.accessioned2024-09-16T00:30:22Z-
dc.date.available2024-09-16T00:30:22Z-
dc.date.issued2023-10-16-
dc.identifier.citationThe Journal of Clinical Investigation, 2023, v. 133, n. 20-
dc.identifier.issn0021-9738-
dc.identifier.urihttp://hdl.handle.net/10722/346351-
dc.description.abstractCarcinogen exposure has been associated with enhanced cancer immunogenicity that is often attributed to neoantigen generation. However, the broader, neoantigen-independent impact of carcinogens on immune responses to cancer cells remains underexplored. In this issue of the JCI, Huang et al. uncover a mechanism wherein carcinogen-treated cancer cells exhibit an inability to establish an immunosuppressive tumor microenvironment (TME) due to reduced M-CSF expression. Intriguingly, the so-called carcinogen-induced tumor-associated macrophages (TAMs) within this TME exhibited anti-tumor properties instead of the conventional immunosuppressive phenotype. This phenomenon extended to human lung cancers, as evidenced by TAM reprogramming in smokers versus nonsmokers. This study substantially advances our understanding of carcinogen-mediated effects on cancer immunogenicity, potentially redirecting approaches to cancer immunotherapy.-
dc.languageeng-
dc.publisherAmerican Society for Clinical Investigation-
dc.relation.ispartofThe Journal of Clinical Investigation-
dc.rightsThis work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.-
dc.titleChemical carcinogens: implications for cancer treatment-
dc.typeArticle-
dc.identifier.doi10.1172/JCI174319-
dc.identifier.pmid37843275-
dc.identifier.scopuseid_2-s2.0-85174749230-
dc.identifier.volume133-
dc.identifier.issue20-
dc.identifier.eissn1558-8238-
dc.identifier.issnl0021-9738-

Export via OAI-PMH Interface in XML Formats


OR


Export to Other Non-XML Formats