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Normal view

  • ✇Nature Cancer
  • Targeting valine metabolism and ferroptosis to overcome chemoresistance in PDAC
    Nature Cancer, Published online: 14 September 2026; doi:10.1038/s43018-026-01235-xWe identified a metabolic signaling axis that enables pancreatic cancer cells to survive chemotherapy by suppressing ferroptosis. Targeting of the valine catabolism enzyme MMSDH reverses this chemoresistance and shows promise as a potential component of combination strategies against refractory tumors.
     

Targeting valine metabolism and ferroptosis to overcome chemoresistance in PDAC

14 September 2026 at 08:00

Nature Cancer, Published online: 14 September 2026; doi:10.1038/s43018-026-01235-x

We identified a metabolic signaling axis that enables pancreatic cancer cells to survive chemotherapy by suppressing ferroptosis. Targeting of the valine catabolism enzyme MMSDH reverses this chemoresistance and shows promise as a potential component of combination strategies against refractory tumors.

MMSDH facilitates ACSL4 propionylation to counteract ferroptosis upon hypoxia and impairs PDAC chemotherapy efficacy

Nature Cancer, Published online: 11 September 2026; doi:10.1038/s43018-026-01236-w

Zheng et al. describe how hypoxia-induced methylmalonate semialdehyde dehydrogenase lactylation promotes acyl-CoA synthetase long-chain family member 4 propionylation and degradation, thereby suppressing ferroptosis induced by chemotherapy, and develop a blocking peptide that increased chemotherapy efficacy in pancreatic ductal adenocarcinoma.

Commensal <i>Nakaseomyces glabratus</i> migrates into prostate tumors to accelerate cancer progression

Nature Cancer, Published online: 09 September 2026; doi:10.1038/s43018-026-01229-9

Lai et al. show that Nakaseomyces glabratus is enriched in fecal and tumor samples of patients with castration-resistant prostate cancer and that administration of the fungus accelerates cancer progression in prostate cancer-bearing castrated mice.
  • ✇Nature Cancer
  • <span>l</span>-Glutamine’s potential to enhance chemotherapy efficacy in advanced pancreatic cancer
    Nature Cancer, Published online: 01 September 2026; doi:10.1038/s43018-026-01231-1The addition of oral l-glutamine to first-line gemcitabine plus nab-paclitaxel appears safe and is associated with improved survival outcomes and tumor responses compared with historical benchmarks in untreated advanced pancreatic cancer. The beneficial effects of l-glutamine may be mediated through modulation of intermediary metabolism, gut microbial function, inflammatory responses and gut barrier integrity.
     

<span>l</span>-Glutamine’s potential to enhance chemotherapy efficacy in advanced pancreatic cancer

1 September 2026 at 08:00

Nature Cancer, Published online: 01 September 2026; doi:10.1038/s43018-026-01231-1

The addition of oral l-glutamine to first-line gemcitabine plus nab-paclitaxel appears safe and is associated with improved survival outcomes and tumor responses compared with historical benchmarks in untreated advanced pancreatic cancer. The beneficial effects of l-glutamine may be mediated through modulation of intermediary metabolism, gut microbial function, inflammatory responses and gut barrier integrity.

SlideChat is a multimodal generative artificial intelligence assistant for whole-slide computational pathology across cancer types

Nature Cancer, Published online: 01 September 2026; doi:10.1038/s43018-026-01220-4

Chen et al. have developed SlideChat, a multimodal generative artificial intelligence assistant, which they benchmark on 27 pathology tasks across 33 cancer types. Expert pathologists rated the assistant as clinically relevant and accurate.

<span>l</span>-Glutamine in combination with first-line gemcitabine and nab-paclitaxel in advanced pancreatic ductal adenocarcinoma: an open-label, single-arm, phase 1 GlutaPanc trial

Nature Cancer, Published online: 31 August 2026; doi:10.1038/s43018-026-01225-z

In this open-label, single-arm, phase 1 GlutaPanc trial, Gong and colleagues report the safety and feasibility of l-glutamine in participants with advanced pancreatic ductal adenocarcinoma and determine the recommended phase 2 dose of l-glutamine in combination with gemcitabine and nab-paclitaxel.

Author Correction: Low-protein diet enhances antitumor immunity in pancreatic cancer through microbiota-derived UDP-galactose

Nature Cancer, Published online: 25 August 2026; doi:10.1038/s43018-026-01241-z

Author Correction: Low-protein diet enhances antitumor immunity in pancreatic cancer through microbiota-derived UDP-galactose

Galanin impairs tumor immunity in glioblastoma by promoting infiltration and ferroptosis resistance of myeloid-derived suppressor cells

Nature Cancer, Published online: 25 August 2026; doi:10.1038/s43018-026-01221-3

Chen and colleagues report that the neuropeptide galanin impairs antitumor immunity in glioblastoma by interacting with its receptor GALR3 on monocytic myeloid-derived suppressor cells, promoting their infiltration and ferroptosis resistance.
  • ✇Nature Cancer
  • Coming full circle Paul S. Mischel
    Nature Cancer, Published online: 21 August 2026; doi:10.1038/s43018-026-01219-xPaul Mischel obtained his MD from Cornell University Medical College, trained in anatomic and neuropathology at UCLA and did post-doctoral research training in Louis Reichardt’s lab at HHMI/UCSF. He is the Fortinet Founders Professor, vice chair for research for the department of pathology, and deputy director of translational science and an institute scholar at Sarafan ChEM-H, Stanford University. Mischel leads Team
     

Coming full circle

21 August 2026 at 08:00

Nature Cancer, Published online: 21 August 2026; doi:10.1038/s43018-026-01219-x

Paul Mischel obtained his MD from Cornell University Medical College, trained in anatomic and neuropathology at UCLA and did post-doctoral research training in Louis Reichardt’s lab at HHMI/UCSF. He is the Fortinet Founders Professor, vice chair for research for the department of pathology, and deputy director of translational science and an institute scholar at Sarafan ChEM-H, Stanford University. Mischel leads Team eDyNAmiC of the Cancer Grand Challenges Program. He is a member of the National Academy of Medicine, a fellow of the AACR Academy, and past president of the American Society for Clinical Investigation.

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.
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