| Literature DB >> 32910905 |
Maayan Baron1, Mohita Tagore2, Miranda V Hunter2, Isabella S Kim2, Reuben Moncada1, Yun Yan1, Nathaniel R Campbell3, Richard M White4, Itai Yanai5.
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.Entities:
Keywords: cancer cell states; drug-resistant states; melanoma; single-cell RNA-seq; spatial transcriptomics; stress-like
Year: 2020 PMID: 32910905 PMCID: PMC8027961 DOI: 10.1016/j.cels.2020.08.018
Source DB: PubMed Journal: Cell Syst ISSN: 2405-4712 Impact factor: 10.304