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- Publisher Website: 10.1172/JCI174319
- Scopus: eid_2-s2.0-85174749230
- PMID: 37843275
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Article: Chemical carcinogens: implications for cancer treatment
Title | Chemical carcinogens: implications for cancer treatment |
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Authors | |
Issue Date | 16-Oct-2023 |
Publisher | American Society for Clinical Investigation |
Citation | The Journal of Clinical Investigation, 2023, v. 133, n. 20 How to Cite? |
Abstract | Carcinogen 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 Identifier | http://hdl.handle.net/10722/346351 |
ISSN | 2023 Impact Factor: 13.3 2023 SCImago Journal Rankings: 4.833 |
DC Field | Value | Language |
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dc.contributor.author | Liu, Shaofeng | - |
dc.contributor.author | Saunders, Mary | - |
dc.contributor.author | Mak, Tak Wah | - |
dc.date.accessioned | 2024-09-16T00:30:22Z | - |
dc.date.available | 2024-09-16T00:30:22Z | - |
dc.date.issued | 2023-10-16 | - |
dc.identifier.citation | The Journal of Clinical Investigation, 2023, v. 133, n. 20 | - |
dc.identifier.issn | 0021-9738 | - |
dc.identifier.uri | http://hdl.handle.net/10722/346351 | - |
dc.description.abstract | Carcinogen 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.language | eng | - |
dc.publisher | American Society for Clinical Investigation | - |
dc.relation.ispartof | The Journal of Clinical Investigation | - |
dc.rights | This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License. | - |
dc.title | Chemical carcinogens: implications for cancer treatment | - |
dc.type | Article | - |
dc.identifier.doi | 10.1172/JCI174319 | - |
dc.identifier.pmid | 37843275 | - |
dc.identifier.scopus | eid_2-s2.0-85174749230 | - |
dc.identifier.volume | 133 | - |
dc.identifier.issue | 20 | - |
dc.identifier.eissn | 1558-8238 | - |
dc.identifier.issnl | 0021-9738 | - |