The Stress-Like Cancer Cell State Is a Consistent Component of Tumorigenesis

Cell Syst. 2020 Nov 18;11(5):536-546.e7. doi: 10.1016/j.cels.2020.08.018. Epub 2020 Sep 9.

Abstract

Transcriptional profiling of tumors has revealed a stress-like state among the cancer cells with the concerted expression of genes such as fos, jun, and heat-shock proteins, though this has been controversial given possible dissociation-effects associated with single-cell RNA sequencing. Here, we validate the existence of this state using a combination of zebrafish melanoma modeling, spatial transcriptomics, and human samples. We found that the stress-like subpopulation of cancer cells is present from the early stages of tumorigenesis. Comparing with previously reported single-cell RNA sequencing datasets from diverse cancer types, including triple-negative breast cancer, oligodendroglioma, and pancreatic adenocarcinoma, indicated the conservation of this state during tumorigenesis. We also provide evidence that this state has higher tumor-seeding capabilities and that its induction leads to increased growth under both MEK and BRAF inhibitors. Collectively, our study supports the stress-like cells as a cancer cell state expressing a coherent set of genes and exhibiting drug-resistance properties.

Keywords: cancer cell states; drug-resistant states; melanoma; single-cell RNA-seq; spatial transcriptomics; stress-like.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adenocarcinoma / genetics
  • Animals
  • Carcinogenesis / metabolism
  • Carcinogenesis / pathology*
  • Cell Line, Tumor
  • Drug Resistance, Neoplasm / genetics
  • Gene Expression / genetics
  • Gene Expression Profiling / methods
  • Gene Expression Regulation, Neoplastic / genetics
  • Humans
  • Melanoma / genetics*
  • Melanoma / metabolism
  • Melanoma / physiopathology
  • Protein Kinase Inhibitors / pharmacology
  • Sequence Analysis, RNA / methods
  • Single-Cell Analysis / methods
  • Stress, Physiological / genetics*
  • Transcriptome / genetics
  • Zebrafish

Substances

  • Protein Kinase Inhibitors