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Highlights in Cancer Research: January 2023

October 17, 2025
Highlights in Cancer Research: November 2022

The EACR’s ‘Highlights in Cancer Research’ is a regular summary of the most interesting and impactful recent papers in cancer research, curated by the Board of the European Association for Cancer Research (EACR).

The list below appears in no particular order, and the summary information has been provided by the authors unless otherwise indicated.

Use the dropdown menu or ‘Previous’ and ‘Next’ buttons to navigate the list.

1. Cancer cell autophagy, reprogrammed macrophages, and remodeled vasculature in glioblastoma triggers tumor immunity

  • 1. Cancer cell autophagy, reprogrammed macrophages, and remodeled vasculature in glioblastoma triggers tumor immunity
  • 2. A noncoding single-nucleotide polymorphism at 8q24 drives IDH1-mutant glioma formation
  • 3. Breast tumor microenvironment structures are associated with genomic features and clinical outcome
  • 4. A covalent inhibitor of K-Ras(G12C) induces MHC class I presentation of haptenated peptide neoepitopes targetable by immunotherapy
  • 5. Chronic exposure to carbon black ultrafine particles reprograms macrophage metabolism and accelerates lung cancer
  • 6. Deep whole-genome ctDNA chronology of treatment-resistant prostate cancer
  • 7. Deciphering the immunopeptidome in vivo reveals new tumour antigens
  • 8. Lung fibroblasts facilitate pre-metastatic niche formation by remodeling the local immune microenvironment
  • 9. RASA2 ablation in T cells boosts antigen sensitivity and long-term function
  • 10. Sensitisation of cancer cells to radiotherapy by serine and glycine starvation
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Chryplewicz, A. et al. Cancer Cell. 40(10):1111-1127. (2022).
doi: 10.1016/j.ccell.2022.08.014.

Summary of the findings

Glioblastoma (GBM) is the most aggressive tumor in the central nervous system. Despite pronounced efforts to identify effective therapies, curative options for GBM do not exist, and the survival rate of diagnosed patients is low. In this paper, the authors took an approach of co-targeting and disrupting distinct features of the immunosuppressive glioma microenvironment, aiming to elicit a sustained therapeutic response. To do so they combined a tricyclic antidepressant (TCA) – imipramine – with a drug targeting VEGF-A ligand in mice bearing de novo GBM. While neither drug was efficacious as monotherapy, the combination of IM + anti-VEGF significantly delayed tumor growth. Investigation of the basis for the therapeutic efficacy revealed that the combo accentuated autophagy in cancer cells while modifying the angiogenic tumor vasculature with induction of high endothelial venules, known to facilitate the extravasation of T cells. Imipramine downregulated a pro-tumorigenic phenotype of tumor-associated macrophages via inhibiting histamine receptor, thereby reprogramming them to express chemokines attracting otherwise rare T cells, which demonstrably contributed functionally to the observed efficacy. As such, this co-targeting regimen reprograms GBM, rendering it immuno-stimulatory and provocatively sensitive to immune checkpoint blockade, as evidenced by sustained therapeutic responses when an anti-PD-L1 therapy was included in the mix.
A combination of tricyclic antidepressants (TCA) and anti-VEGF treatment increases autophagic flux, reprogrammes tumour-associated macrophages and remodels vascular in glioblastoma rendering the tumour susceptible to immunotherapy such as anti-PD-L1 therapy.

Future impact

This investigation has revealed a provocative new therapeutic approach involving clinically approved drugs that unleashed a potent anti-tumoral immune response in a tumor type that is otherwise refractory to immune intervention. Given the transient response and the dismal prognosis of GBM patients on standard-of-care therapies, these findings motivate consideration of proof-of-concept clinical trials aimed to evaluate the translational potential of TCAs combined with VEGF pathway inhibitors and immune checkpoint blockade. Notably, this study has motivated the Mark Foundation to support a clinical trial in GBM patients progressing on first-line treatment.

Read more in Cancer Cell

 

1. Cancer cell autophagy, reprogrammed macrophages, and remodeled vasculature in glioblastoma triggers tumor immunity

  • 1. Cancer cell autophagy, reprogrammed macrophages, and remodeled vasculature in glioblastoma triggers tumor immunity
  • 2. A noncoding single-nucleotide polymorphism at 8q24 drives IDH1-mutant glioma formation
  • 3. Breast tumor microenvironment structures are associated with genomic features and clinical outcome
  • 4. A covalent inhibitor of K-Ras(G12C) induces MHC class I presentation of haptenated peptide neoepitopes targetable by immunotherapy
  • 5. Chronic exposure to carbon black ultrafine particles reprograms macrophage metabolism and accelerates lung cancer
  • 6. Deep whole-genome ctDNA chronology of treatment-resistant prostate cancer
  • 7. Deciphering the immunopeptidome in vivo reveals new tumour antigens
  • 8. Lung fibroblasts facilitate pre-metastatic niche formation by remodeling the local immune microenvironment
  • 9. RASA2 ablation in T cells boosts antigen sensitivity and long-term function
  • 10. Sensitisation of cancer cells to radiotherapy by serine and glycine starvation
Previous
Next
Tags: EACR Top Ten Cancer Research PublicationsHighlights in Cancer Research

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