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Copper depletion boosts CNS leukemia therapy by inhibiting nucleotide synthesis through impairment of mitochondrial complex IV activity

Nature Cancer, Published online: 25 May 2026; doi:10.1038/s43018-026-01177-4

Wong et al. uncover a nutritional dependency for acute lymphoblastic leukemia cells that spread to the central nervous system and propose using copper restriction to impair leukemia progression by disrupting nucleotide synthesis through the inhibition of electron transport chain activity.

Tumor irradiation promotes antigen dressing of dendritic cells to enhance CAR T cell persistence and efficacy in lung metastases

Nature Cancer, Published online: 22 May 2026; doi:10.1038/s43018-026-01167-6

Ahmed and colleagues show that, by promoting ‘dressing’ of intact tumor target antigens onto dendritic cells, tumor irradiation enhances chimeric antigen receptor T cell persistence and efficacy in lung metastasis models.

Coupling dead cell recognition to Fcγ receptors augments anticancer immunity

Nature Cancer, Published online: 20 May 2026; doi:10.1038/s43018-026-01168-5

Castro-Dopico et al. report the design of reagents to bridge F-actin and Fcγ receptors, endowing a range of antigen-presenting cells with the ability to cross-present antigens from dead tumor cells and boosting antitumor immunity in preclinical models.

Targeting cysteinyl leukotriene receptor 1 reprograms tumor-promoting myelopoiesis and overcomes immune checkpoint therapy resistance

Nature Cancer, Published online: 19 May 2026; doi:10.1038/s43018-026-01174-7

Tang et al. identify cysteinyl leukotriene receptor 1 (CysLTR1) as a critical regulator of tumor-induced myelopoiesis, suggesting CysLTR1 targeting to sensitize tumors to immune checkpoint blockade.
  • ✇Nature Cancer
  • Immunological outcomes of a bespoke DNA cancer vaccine in glioblastoma
    Nature Cancer, Published online: 18 May 2026; doi:10.1038/s43018-026-01162-xWe report the results of a phase 1 clinical trial (NCT04015700) evaluating the safety and immunogenicity of GNOS-PV01, a personalized DNA cancer vaccine, in patients with MGMT-unmethylated glioblastoma, after surgery and radiotherapy. Immune responses were detected in all but one patient, who received immunosuppressive steroids. The 24-month overall survival was 33%, including one patient who was alive more than 48 month
     

Immunological outcomes of a bespoke DNA cancer vaccine in glioblastoma

18 May 2026 at 08:00

Nature Cancer, Published online: 18 May 2026; doi:10.1038/s43018-026-01162-x

We report the results of a phase 1 clinical trial (NCT04015700) evaluating the safety and immunogenicity of GNOS-PV01, a personalized DNA cancer vaccine, in patients with MGMT-unmethylated glioblastoma, after surgery and radiotherapy. Immune responses were detected in all but one patient, who received immunosuppressive steroids. The 24-month overall survival was 33%, including one patient who was alive more than 48 months after diagnosis.

CD300ld on pathologically activated neutrophils promotes tumor immune suppression by binding phosphatidylserine on CD8<sup>+</sup> T cells

Nature Cancer, Published online: 15 May 2026; doi:10.1038/s43018-026-01169-4

Zhao and colleagues show that CD300ld, upregulated in pathologically activated neutrophils, mediates contact-dependent suppression of cytotoxic CD8+ T cells by binding to phosphatidylserine, inhibiting antitumor immune responses.

Combined ctDNA and serum PSA for dynamic monitoring of metastatic prostate cancer starting first-line treatment: a prospective national cohort study

Nature Cancer, Published online: 15 May 2026; doi:10.1038/s43018-026-01172-9

Jayaram et al. assessed the performance of the combination of circulating tumor DNA and serum prostate-specific antigen for dynamic monitoring of metastatic prostate cancer at first-line treatment in this prospective observational clinical trial.
  • ✇Nature Cancer
  • Harnessing foundation models for digital pathology without re-training Zhiping Xiao · Sheng Wang
    Nature Cancer, Published online: 03 April 2026; doi:10.1038/s43018-025-01108-9Applications of digital pathology in clinical oncology have largely depended on the requirement for labeled data and model re-training. A study now presents PRET, a training-free framework with robust performance for pan-cancer diagnosis that adapts pathology foundation models to diverse tasks at inference stage, from screening and subtyping tasks to segmentation and metastasis detection tasks.
     

Harnessing foundation models for digital pathology without re-training

3 April 2026 at 08:00

Nature Cancer, Published online: 03 April 2026; doi:10.1038/s43018-025-01108-9

Applications of digital pathology in clinical oncology have largely depended on the requirement for labeled data and model re-training. A study now presents PRET, a training-free framework with robust performance for pan-cancer diagnosis that adapts pathology foundation models to diverse tasks at inference stage, from screening and subtyping tasks to segmentation and metastasis detection tasks.

A tumor-derived metabolite primes the leptomeningeal pre-metastatic niche

3 April 2026 at 08:00

Nature Cancer, Published online: 03 April 2026; doi:10.1038/s43018-026-01138-x

Leptomeningeal metastases are a devastating complication of solid tumors; how this niche becomes pro-metastatic remains poorly understood. A study now reveals that tumor cells prime a pre-metastatic niche within the leptomeninges via exosome-derived 5-HIAA, triggering vascular leakiness and accumulation of disseminated tumor cells.

Leptomeningeal metastatic cancer cells induce a permissive choroid plexus vasculature through extracellular-vesicle-derived 5-HIAA signaling

Nature Cancer, Published online: 03 April 2026; doi:10.1038/s43018-026-01145-y

Huang, Hou, Yang et al. demonstrate that leptomeningeal metastatic cells favor the formation of a premetastatic niche by remodeling the choroid plexus vasculature through the serotonin metabolite 5-hydroxyindoleacetic acid, which signals into endothelial cells through the aryl hydrocarbon receptor.

PRET is a few-shot system for pan-cancer recognition without example training

Nature Cancer, Published online: 03 April 2026; doi:10.1038/s43018-026-01141-2

Li et al. present PRET, a few-shot system for pan-cancer detection not requiring model fine-tuning, validated it in multicenter datasets and found that it outperformed existing approaches across tasks and pathologists in lymph node metastasis detection.

Single-cell and spatial profiling in cancer biology and clinical oncology

Nature Cancer, Published online: 03 April 2026; doi:10.1038/s43018-026-01142-1

Izar and colleagues review the insights into cancer biology gained via single-cell analyses and spatial profiling and overview the challenges and opportunities associated with the implementation of these approaches to guide clinical discovery.

Decoding pediatric brain tumors via CSF-derived methylomes

30 March 2026 at 08:00

Nature Cancer, Published online: 30 March 2026; doi:10.1038/s43018-026-01139-w

Cerebrospinal fluid (CSF)-derived cell-free DNA holds promise for CNS tumors, but its limited yield poses challenges. A study now presents M-PACT, a framework that uses sub-nanogram CSF-derived cell-free DNA methylomes for tumor classification, paving the way for minimally invasive diagnosis of pediatric brain tumors.
  • ✇Nature Cancer
  • A functional map of m<sup>6</sup>A sites in cancer Yalong Wang · Han Xu
    Nature Cancer, Published online: 13 March 2026; doi:10.1038/s43018-026-01137-yRNA N6-methyladenosine (m6A) is the most abundant internal RNA modification, yet its functional landscape in cancer remains poorly defined. A study now introduces a METTL3-based RNA base-editing screen that maps functional m6A sites and reveals m6A-dependent translational activation of the tumor suppressor CHD9 in prostate cancer and beyond.
     

A functional map of m<sup>6</sup>A sites in cancer

13 March 2026 at 08:00

Nature Cancer, Published online: 13 March 2026; doi:10.1038/s43018-026-01137-y

RNA N6-methyladenosine (m6A) is the most abundant internal RNA modification, yet its functional landscape in cancer remains poorly defined. A study now introduces a METTL3-based RNA base-editing screen that maps functional m6A sites and reveals m6A-dependent translational activation of the tumor suppressor CHD9 in prostate cancer and beyond.

The genomic model P-CARE enables precision prostate cancer screening in a national healthcare system

13 March 2026 at 08:00

Nature Cancer, Published online: 13 March 2026; doi:10.1038/s43018-025-01111-0

We developed and clinically implemented the genomic prostate cancer risk prediction model P-CARE that identifies men at a high or low risk of prostate cancer. P-CARE enabled the design and initiation of a precision screening trial across the national healthcare system in which it was developed.
  • ✇Nature Cancer
  • AI for breast cancer screening Allan Hackshaw · Rosalind Given-Wilson
    Nature Cancer, Published online: 10 March 2026; doi:10.1038/s43018-025-01109-8Whether support from artificial intelligence (AI) models improves breast screening is a topic of research in national cancer screening programmes and clinical oncology. Three studies now show that AI tools can assist radiologists with evaluating mammograms, substantially reducing workloads and possibly improving screening performance.
     

AI for breast cancer screening

10 March 2026 at 08:00

Nature Cancer, Published online: 10 March 2026; doi:10.1038/s43018-025-01109-8

Whether support from artificial intelligence (AI) models improves breast screening is a topic of research in national cancer screening programmes and clinical oncology. Three studies now show that AI tools can assist radiologists with evaluating mammograms, substantially reducing workloads and possibly improving screening performance.
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