Tumor-Infiltrating Myeloid Cells Co-Express TREM1 and TREM2 and Elevated TREM-1 Associates With Disease Progression in Renal Cell Carcinoma.

TREM family TREM1 TREM2 (triggering receptor expressed on myeloid cells) myeloid-derived suppressor cell renal cell carcinoma sTREM-1 tumor-associated macrophage

Journal

Frontiers in oncology
ISSN: 2234-943X
Titre abrégé: Front Oncol
Pays: Switzerland
ID NLM: 101568867

Informations de publication

Date de publication:
2021
Historique:
received: 08 02 2021
accepted: 27 09 2021
entrez: 28 2 2022
pubmed: 1 3 2022
medline: 1 3 2022
Statut: epublish

Résumé

Myeloid-derived suppressor cells (MDSC) and tumor-associated macrophages (TAM) contribute to cancer-related inflammation and tumor progression. While several myeloid molecules have been ascribed a regulatory function in these processes, the triggering receptors expressed on myeloid cells (TREMs) have emerged as potent modulators of the innate immune response. While various TREMs amplify inflammation, others dampen it and are emerging as important players in modulating tumor progression-for instance, soluble TREM-1 (sTREM-1), which is detected during inflammation, associates with disease progression, while TREM-2 expression is associated with tumor-promoting macrophages. We hypothesized that TREM-1 and TREM-2 might be co-expressed on tumor-infiltrating myeloid cells and that elevated sTREM-1 associates with disease outcomes, thus representing a possibility for mutual modulation in cancer. Using the 4T1 breast cancer model, we found TREM-1 and TREM-2 expression on MDSC and TAM and that sTREM-1 was elevated in tumor-bearing mice in multiple models and correlated with tumor volume. While TREM-1 engagement enhanced TNF, a TREM-2 ligand was detected on MDSC and TAM, suggesting that both TREM could be functional in the tumor setting. Similarly, we detected TREM-1 and

Identifiants

pubmed: 35223446
doi: 10.3389/fonc.2021.662723
pmc: PMC8867210
doi:

Types de publication

Journal Article

Langues

eng

Pagination

662723

Informations de copyright

Copyright © 2021 Ford, Gonzalez-Cotto, MacFarlane, Peri, Howard, Subleski, Ruth, Haseebuddin, Al-Saleem, Yang, Rayman, Rini, Linehan, Finke, Weiss, Campbell and McVicar.

Déclaration de conflit d'intérêts

Author BR: Research Funding to Institution: Pfizer, Hoffman-LaRoche, Incyte, AstraZeneca, Seattle Genetics, Arrowhead Pharmaceuticals, Immunomedics, BMS, Mirati Therapeutics, Merck, Surface Oncology, Dragonfly Therapeutics, Aravive, Exelixis, Jannsen. Consulting: BMS, Pfizer, GNE/Roche, Aveo, Synthorx, Compugen, Merck, Corvus, Surface Oncology, 3DMedicines, Aravive, Alkermes, Arrowhead, GSK, Shionogi, Eisai, Nikang Therapeutics. Stock: PTC therapeutics. The remaining authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

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Auteurs

Jill W Ford (JW)

Laboratory of Cancer Immunometabolism, National Cancer Institute (NCI), Frederick, MD, United States.

Marieli Gonzalez-Cotto (M)

Laboratory of Cancer Immunometabolism, National Cancer Institute (NCI), Frederick, MD, United States.

Alexander W MacFarlane (AW)

Blood Cell Development and Function Program, Institute for Cancer Research, Philadelphia, PA, United States.

Suraj Peri (S)

Biostatistics and Bioinformatics Facility, Fox Chase Cancer Center, Philadelphia, PA, United States.

O M Zack Howard (OMZ)

Laboratory of Cancer Immunometabolism, National Cancer Institute (NCI), Frederick, MD, United States.

Jeffrey J Subleski (JJ)

Laboratory of Cancer Immunometabolism, National Cancer Institute (NCI), Frederick, MD, United States.

Karen J Ruth (KJ)

Biostatistics and Bioinformatics Facility, Fox Chase Cancer Center, Philadelphia, PA, United States.

Mohammed Haseebuddin (M)

Department of Surgical Oncology, Fox Chase Cancer Center, Philadelphia, PA, United States.

Tahseen Al-Saleem (T)

Department of Pathology, Fox Chase Cancer Center, Philadelphia, PA, United States.

Youfeng Yang (Y)

Urologic Oncology Branch, National Cancer Institute (NCI), Bethesda, MD, United States.

Pat Rayman (P)

Cleveland Clinic, Department of Immunology, Lerner Research Institute, Cleveland, OH, United States.

Brian Rini (B)

Cleveland Clinic, Department of Solid Tumor Oncology, Cleveland, OH, United States.

W Marston Linehan (WM)

Urologic Oncology Branch, National Cancer Institute (NCI), Bethesda, MD, United States.

James Finke (J)

Cleveland Clinic, Department of Immunology, Lerner Research Institute, Cleveland, OH, United States.

Jonathan M Weiss (JM)

Laboratory of Cancer Immunometabolism, National Cancer Institute (NCI), Frederick, MD, United States.

Kerry S Campbell (KS)

Blood Cell Development and Function Program, Institute for Cancer Research, Philadelphia, PA, United States.

Daniel W McVicar (DW)

Laboratory of Cancer Immunometabolism, National Cancer Institute (NCI), Frederick, MD, United States.

Classifications MeSH