Aller au contenu principal
2026 conference-abstract

Abstract 778: Hypoxia shapes tumor immune microenvironment through cell-type dependent responses in diffuse astrocytomas.

0Citations signalées, ce qui n’est pas une note de qualité
5Institutions déclarées
2Pays d’affiliation déclarés

Rattachement africain : fi, de. Niveau de preuve : code pays fourni par la source.

Le résumé fourni par la source

Abstract Background: Hypoxia is a critical driver of tumor aggressiveness in high-grade gliomas, yet its cell-type-specific effects on immune cell populations within the tumor microenvironment (TME) remain poorly understood. Materials and methods: We have investigated how hypoxia shapes the spatial distribution and functional states of monocyte-derived macrophages (MDMs) and brain-resident microglia (MG) in diffuse astrocytomas and glioblastomas (GB) by using cyclic immunohistochemistry (cIHC), single-cell RNA sequencing, spatial transcriptomics, and in vitro cell culture models in controlled oxygen and pH conditions. Results: Hypoxia induces divergent responses in these myeloid subsets, driving spatial immune patterning. In GB, CD163- MDMs dominate hypoxic niches, while MG populations are excluded from these regions, correlating with hypoxia-induced TNF upregulation, stress response signatures, and dampened interferon responses. Conversely, MDMs exhibit a shift towards hypoxia-associated immunosuppressive traits, altered metabolism and upregulated cell survival. GBs display elevated hypoxic intensity compared to diffuse astrocytomas, as supported by hypoxia-response gene expression in the TCGA dataset. In vitro, MG are characterized by heightened sensitivity to hypoxia-associated acidity compared to MDMs, suggesting that their exclusion from hypoxic zones results from intrinsic vulnerability. Conclusion: Our findings reveal that hypoxia and hypoxia-associated acidity remodel the TME by promoting immunosuppressive MDM accumulation and depletion of MG, creating spatially distinct immune landscapes that may underlie GB progression. These results highlight hypoxia-driven immune dysregulation as a therapeutic target and underscore the importance of cell-type-specific strategies to counteract TME-driven immunosuppression in malignant gliomas. Citation Format: Aliisa Tiihonen, Iida Salonen, Iina Koivisto, Anni Ritamäki, Serafiina Jaatinen, Tanja Hyvärinen, Johanna Tilvis, Joose Kreutzer, Masi Valkonen, Göktug Karabiyik, Sonja Mäntylä, Maryam Mohammadlou, Miina Hoikka, Jürgen Beck, Roland Rölz, Mikael Marttinen, Matti Nykter, Joonas Haapasalo, Pekka Ruusuvuori, Seppo Parkkila, Pasi Kallio, Sanna Hagman, Juha Kesseli, Vidhya Madapusi Ravi, Hannu Haapasalo, Arja Jukkola, Kevin Joseph, Kirsi Rautajoki. Hypoxia shapes tumor immune microenvironment through cell-type dependent responses in diffuse astrocytomas [abstract]. In: Proceedings of the American Association for Cancer Research Annual Meeting 2026; Part 1 (Regular Abstracts); 2026 Apr 17-22; San Diego, CA. Philadelphia (PA): AACR; Cancer Res 2026;86(7 Suppl):Abstract nr 778.

Ce résumé expose les affirmations des auteurs. BNTIC ne l’interprète pas comme une validation indépendante des résultats.

Le contrôle bibliographique ouvert

DOI retrouvé dans Crossref DOI retrouvé ; titre concordant.

Titre Crossref
Abstract 778: Hypoxia shapes tumor immune microenvironment through cell-type dependent responses in diffuse astrocytomas.
Date Crossref
03/04/2026
Éditeur
American Association for Cancer Research (AACR)
Type
journal-article

Ce recoupement confirme des métadonnées liées au DOI. Il ne confirme ni la méthode ni les conclusions de l’étude, et il ne compte pas comme une seconde source scientifique indépendante.

Les institutions déclarées

Une affiliation ne permet pas de déduire la nationalité d’un auteur.

Les sujets associés

Cancer, Hypoxia, and MetabolismImmune cells in cancerFerroptosis and cancer prognosis

BNTIC News n’est pas le producteur de ces données. Les publications sont interrogées à la demande dans Crossref, OpenAIRE, DOAJ, Europe PMC, HAL, DataCite, AfricArXiv, ROR et la Banque mondiale, sans clé d’accès. OpenAlex reste optionnel. Aucun service payant n’est nécessaire et aucune donnée externe n’est enregistrée en base. Consulter les sources et leurs limites.