PDAC heterogeneity resolved spatially at the single-cell level: new biological answers, new questions on optimal translation

J Pathol. 2024 Aug;263(4-5):397-399. doi: 10.1002/path.6293. Epub 2024 Jun 3.

Abstract

Pancreatic cancer is a highly aggressive disease. Developing new strategies and using powerful methodologies for its early detection, coupled with in-depth comprehension of the mechanisms governing subtype evolution, will not only help to stratify PDAC patients' prognosis but also prevent unfavourable subtype plasticity upon treatment with chemotherapy. Michiels et al have developed a new approach to better capture PDAC heterogeneity at the single tumour duct spatial resolution level, leveraging detection of transcripts for mutant KRAS and multiple subtype markers. Their study sheds light on the association of mutant KRAS and PDAC phenotypic heterogeneity. The findings support functional cooperation of plastic tumour cells and opens new challenges towards PDAC patient stratification and therapeutic intervention. Pathology-based tools will be of prime importance to address these issues in a clinically meaningful manner. © 2024 The Pathological Society of Great Britain and Ireland.

Keywords: KRAS; molecular heterogeneity; pancreatic cancer; plasticity; spatial biology; transcriptomic subtypes.

Publication types

  • Research Support, Non-U.S. Gov't
  • Comment

MeSH terms

  • Biomarkers, Tumor / genetics
  • Biomarkers, Tumor / metabolism
  • Carcinoma, Pancreatic Ductal* / genetics
  • Carcinoma, Pancreatic Ductal* / pathology
  • Genetic Heterogeneity
  • Humans
  • Mutation
  • Pancreatic Neoplasms* / genetics
  • Pancreatic Neoplasms* / pathology
  • Phenotype
  • Proto-Oncogene Proteins p21(ras) / genetics
  • Single-Cell Analysis* / methods

Substances

  • Biomarkers, Tumor
  • Proto-Oncogene Proteins p21(ras)
  • KRAS protein, human