# Wellcome Sanger atlas of 12 glioblastomas shows cancer cells follow a shared state trajectory

- Published: 2026-11-05 12:37 UTC
- Section: Life & Health › Medicine
- Tags: glioblastoma heterogeneity, single-cell multi-omic atlas, spatial transcriptomics Visium, cancer cell state trajectory, glial injury response, hypoxia in tumours, tumour subclones, patient-derived organoids, GBM-space, myeloid cells in glioblastoma
- URL: https://realtech.media/news/rt-db7c1fc6ac8be62b27c1cb66_wellcome_sanger_atlas/

**An atlas of 12 human glioblastomas and more than 1 million nuclei shows cells shifting from developmental-like states to injury response and hypoxia in a pattern shared across tumours.**

![Wellcome Sanger atlas of 12 glioblastomas shows cancer cells follow a shared state trajectory](https://sgzwpqqelzmajkcubgkl.supabase.co/storage/v1/object/public/rt-media/2026/11/08ede06049a429e5.png)
*nature.com*

Researchers from the Wellcome Sanger Institute, EMBL, the German Cancer Research Center (DKFZ), the Cancer Research UK Cambridge Institute and collaborators built a single-cell and spatial multi-omic atlas of 12 human glioblastomas, according to a paper in Nature (nature.com) published on 4 November [1]. The authors report that tumour heterogeneity follows a spatially patterned transition of cancer cells from developmental-like states to states defined by a glial injury response and hypoxia [1].

## Atlas design

The set covers 12 primary IDH wild-type tumours sampled at 57 sites in total. Most cases were sampled at 4 sites of roughly 1.25 cm3 each, and one tumour at 15 sites, effectively covering it whole [1]. Each site was profiled with paired single-nuclei joint RNA and chromatin accessibility sequencing and with Visium spatial transcriptomics on consecutive sections. Selected sites also received Xenium spatial transcriptomics, immunohistochemistry and whole-genome sequencing of tumour microbiopsies [1].

The dataset includes more than 1 million nuclei (657,275 malignant and 368,054 from the tumour microenvironment) and more than 0.3 million spatial transcriptomes across 97 Visium sections. It is available at gbmspace.org [1].

## Trajectory of cancer cells

The transition divides tumours into distinct tissue microenvironments. It appears in a molecularly conserved form across tumours and across genetically distinct subclones [1]. Using a new computational framework that maps cell states together with clones in situ, the authors found that subclones are finely intermixed within these microenvironments [1].

The trajectory was validated with hierarchies based on somatic mutations in vivo and with a patient-derived organoid model ex vivo. The authors also report that it is linked to myeloid heterogeneity and unfolds across regionalized myeloid signalling environments [1].

According to the release, a companion Nature paper used the same data to identify gene regulators that drive and restrict transitions between cell states.

## Glioblastoma background

Glioblastoma is an incurable adult brain cancer. Per the release, about 3,200 people are diagnosed with it in the UK each year, average survival is 12 to 18 months, and 4 per cent of patients survive five years or more. The work is a laboratory atlas study, not a treatment trial.

## Sources

1. [nature.com](https://www.nature.com/articles/s41586-026-11234-8)
2. [EurekAlert](https://www.eurekalert.org/news-releases/1149933)

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Source: RealTech, realtech.media — https://realtech.media/news/rt-db7c1fc6ac8be62b27c1cb66_wellcome_sanger_atlas/