Skip to content
DraconiticResearch
Search Sources API
203,203 studies31 sourcesUpdated 5 min ago
PreprintCC BY-NC-NDbioRxiv

Age-associated transcriptional programs in tumor-associated macrophages are associated with tumor progression in HPV-negative oral cancer

  1. 1University of Texas MD Anderson Cancer Center

Abstract

Aging and tobacco exposure are major determinants of risk and outcome in HPV-negative oral cavity squamous cell carcinoma (OSCC), yet the cellular programs linking host factors to tumor immunity remain poorly defined. We reprocessed and reanalyzed previously published single-cell RNA-seq data from 19 HPV-negative OSCC tumors and we identified a robust age- and smoking-associated expansion of SPP1high tumor-associated macrophages (TAMs), accompanied by a shift toward a myeloid-dominant and lymphocyte-reduced tumor microenvironment. SPP1high TAMs exhibit a distinct transcriptional state enriched for extracellular-matrix remodeling and metabolic programs and reduced antigen-presentation pathways. They also express inflammatory chemokines such as CXCL2 and CXCL3 and down-regulate the cytotoxic mediator TNFSF10, suggesting a broadly protumor TAM phenotype. Ligand-receptor modeling suggests that SPP1high TAMs act as key communication hubs, with dominant SPP1-CD44 signaling to T-cell subsets. Transcription-factor analysis further implicates a POU2F1/POU2F2/SP1 module in maintaining this state. In the TCGA HNSCC cohort, the association between SPP1 expression and overall survival did not reach statistical significance after adjustment for age and tumor purity. These findings demonstrate that aging and tobacco exposure converge to expand an SPP1high TAM population that remodels the extracellular matrix and suppresses antitumor immunity, highlighting the SPP1-CD44 axis and its upstream regulators as potential therapeutic targets in high-risk OSCC.

Related

  1. Autumn–winter progression triggers distinct transcriptional programs in Arabidopsis thaliana
    Mélanie Ormancey, Benjamin Tremblay, Yajiao Cheng +5
    Genome BiologyPeer-reviewedCC BY 4.0Plant biologyHALCrossref
  2. Reprogramming tumor-associated macrophages in breast cancer: from myeloid plasticity and tumor-promoting programs to CAR-macrophage therapy.
    Farshad Heydari, Mehdi Derakhshani, Jalal Naghinezhad
    Journal of hematology & oncologyPeer-reviewedCC BY-NC-NDFull textImmunologyEurope PMCDOAJ
  3. Enhanced Synaptic-Related Transcriptional Programs in Human Forebrain Organoids for Modeling Synaptopathy-Associated Neurodevelopmental Disorders
    Xiu-Ping Zhang, Ling-Liang Zhang, Xi-Yuan Wang +2
    CellsPeer-reviewedCC BY 4.0Full textNeuroscienceCrossrefEurope PMC
  4. SEC31A promotes gastric cancer progression by inducing the PI3K/AKT/mTOR pathway and enhancing the CCL5-mediated M2 polarization and recruitment of tumor-associated macrophages
    Xixian Zhao, Liuye Huang
    Oncology ReportsPeer-reviewedCC BY-NC-ND 4.0Full textImmunologyPMC
  5. Oxeiptosis-associated transcriptional states, immune heterogeneity, and oxidative-stress susceptibility in triple-negative breast cancer
    Ziyun Zhuang, Haiyu Zhang, Jiawei Lei +4
    Frontiers in ImmunologyPeer-reviewedCC BY 4.0ImmunologyCrossref
BibTeX
@misc{gujar2026ageassociated,
  title = {{Age-associated transcriptional programs in tumor-associated macrophages are associated with tumor progression in HPV-negative oral cancer}},
  author = {H. Gujar and S. Hanache and S. Aggarwal},
  howpublished = {bioRxiv},
  year = {2026},
  month = oct,
  doi = {10.64898/2026.10.02.756061},
  url = {https://www.biorxiv.org/content/10.64898/2026.10.02.756061v1},
  note = {CC BY-NC-ND},
}
RIS
TY  - UNPB
TI  - Age-associated transcriptional programs in tumor-associated macrophages are associated with tumor progression in HPV-negative oral cancer
AU  - H. Gujar
AU  - S. Hanache
AU  - S. Aggarwal
PY  - 2026
DA  - 2026/10/02
PB  - bioRxiv
DO  - 10.64898/2026.10.02.756061
UR  - https://www.biorxiv.org/content/10.64898/2026.10.02.756061v1
AB  - Aging and tobacco exposure are major determinants of risk and outcome in HPV-negative oral cavity squamous cell carcinoma (OSCC), yet the cellular programs linking host factors to tumor immunity remain poorly defined. We reprocessed and reanalyzed previously published single-cell RNA-seq data from 19 HPV-negative OSCC tumors and we identified a robust age- and smoking-associated expansion of SPP1high tumor-associated macrophages (TAMs), accompanied by a shift toward a myeloid-dominant and lymphocyte-reduced tumor microenvironment. SPP1high TAMs exhibit a distinct transcriptional state enriched for extracellular-matrix remodeling and metabolic programs and reduced antigen-presentation pathways. They also express inflammatory chemokines such as CXCL2 and CXCL3 and down-regulate the cytotoxic mediator TNFSF10, suggesting a broadly protumor TAM phenotype. Ligand-receptor modeling suggests that SPP1high TAMs act as key communication hubs, with dominant SPP1-CD44 signaling to T-cell subsets. Transcription-factor analysis further implicates a POU2F1/POU2F2/SP1 module in maintaining this state. In the TCGA HNSCC cohort, the association between SPP1 expression and overall survival did not reach statistical significance after adjustment for age and tumor purity. These findings demonstrate that aging and tobacco exposure converge to expand an SPP1high TAM population that remodels the extracellular matrix and suppresses antitumor immunity, highlighting the SPP1-CD44 axis and its upstream regulators as potential therapeutic targets in high-risk OSCC.
ER  -