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The EACR’s Top 10 Cancer Research Publications: February 2021

October 17, 2025
EACR top 10 cancer research publications

The EACR’s Top 10 Cancer Research Publications is a regular summary of the most interesting and impactful recent papers in cancer research. It is 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.

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

10. Colorectal Cancer Cells Enter a Diapause-like DTP State to Survive Chemotherapy

  • 1. Cross-reactivity between tumor MHC class I–restricted antigens and an enterococcal bacteriophage
  • 2. A Potent and Selective Small-Molecule Degrader of STAT3 Achieves Complete Tumor Regression In Vivo
  • 3. Discovering functional evolutionary dependencies in human cancers
  • 4. High-dose vitamin C enhances cancer immunotherapy
  • 5. Circulating tumour cell clustering shapes DNA methylation to enable metastasis seeding
  • 6. Peripheral CD8+ T cell characteristics associated with durable responses to immune checkpoint blockade in patients with metastatic melanoma
  • 7. Immune-awakening revealed by peripheral T cell dynamics after one cycle of immunotherapy
  • 8. The next entry on the list is two linked papers:
  • 9. MTOR signaling orchestrates stress-induced mutagenesis, facilitating adaptive evolution in cancer
  • 10. Colorectal Cancer Cells Enter a Diapause-like DTP State to Survive Chemotherapy
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S. Rehman, J. Haynes, E. Collignon et al. Cell Volume 184, Issue 1, P226-242.E21, January 07, 2021

“This paper shows evidence that cancer cells which survive therapy enter an embional like state.” Rene Bernards, EACR Board Member

Summary of the findings

Cancer cells enter a reversible drug-tolerant persister (DTP) state to evade death from chemotherapy and targeted agents. It is increasingly appreciated that DTPs are important drivers of therapy failure and tumor relapse. We combined cellular barcoding and mathematical modeling in patient-derived colorectal cancer models to identify and characterize DTPs in response to chemotherapy. Barcode analysis revealed no loss of clonal complexity of tumors that entered the DTP state and recurred following treatment cessation. Our data fit a mathematical model where all cancer cells, and not a small subpopulation, possess an equipotent capacity to become DTPs. Mechanistically, we determined that DTPs display remarkable transcriptional and functional similarities to diapause, a reversible state of suspended embryonic development triggered by unfavorable environmental conditions. Our study provides insight into how cancer cells use a developmentally conserved mechanism to drive the DTP state, pointing to novel therapeutic opportunities to target DTPs.

Read more in Cell

 

10. Colorectal Cancer Cells Enter a Diapause-like DTP State to Survive Chemotherapy

  • 1. Cross-reactivity between tumor MHC class I–restricted antigens and an enterococcal bacteriophage
  • 2. A Potent and Selective Small-Molecule Degrader of STAT3 Achieves Complete Tumor Regression In Vivo
  • 3. Discovering functional evolutionary dependencies in human cancers
  • 4. High-dose vitamin C enhances cancer immunotherapy
  • 5. Circulating tumour cell clustering shapes DNA methylation to enable metastasis seeding
  • 6. Peripheral CD8+ T cell characteristics associated with durable responses to immune checkpoint blockade in patients with metastatic melanoma
  • 7. Immune-awakening revealed by peripheral T cell dynamics after one cycle of immunotherapy
  • 8. The next entry on the list is two linked papers:
  • 9. MTOR signaling orchestrates stress-induced mutagenesis, facilitating adaptive evolution in cancer
  • 10. Colorectal Cancer Cells Enter a Diapause-like DTP State to Survive Chemotherapy
Previous
Next
Tags: EACR BoardEACR Top Ten Cancer Research Publicationspublication

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The EACR, a registered charity, is a global community for those working and studying in cancer research. Our mission is “The advancement of cancer research for the public benefit: from basic research to prevention, treatment and care.”

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