Stem-cell states converge in multistage cutaneous squamous cell carcinoma development

Author:

Taylor Mark A.12ORCID,Kandyba Eve1ORCID,Halliwill Kyle13,Delrosario Reyno1,Khoroshkin Matvei1ORCID,Goodarzi Hani1456ORCID,Quigley David157ORCID,Li Yun Rose18910ORCID,Wu Di1,Bollam Saumya R.11ORCID,Mirzoeva Olga K.1ORCID,Akhurst Rosemary J.112ORCID,Balmain Allan14ORCID

Affiliation:

1. Helen Diller Family Comprehensive Cancer Center, University of California San Francisco, San Francisco, CA 94158, USA.

2. Clinical Research Centre, Medical University of Bialystok, Bialystok 15-089, Poland.

3. AbbVie, South San Francisco, CA 94080, USA.

4. Department of Biochemistry and Biophysics, University of California San Francisco, San Francisco, CA 94518, USA.

5. Department of Urology, University of California San Francisco, San Francisco, CA 94518, USA.

6. Arc Institute, Palo Alto, CA 94304, USA.

7. Department of Epidemiology & Biostatistics, University of California San Francisco, San Francisco, CA 94518, USA.

8. Department of Radiation Oncology, City of Hope National Medical Center, Duarte, CA 91010, USA.

9. Department of Cancer Genetics & Epigenetics, City of Hope National Medical Center, Duarte, CA 91010, USA.

10. Division of Quantitative Medicine & Systems Biology, Translational Genomics Research Institute, Phoenix, CA 85004, USA.

11. Biomedical Sciences Graduate Program, University of California San Francisco, San Francisco, CA 94518, USA.

12. Department of Anatomy, University of California San Francisco, San Francisco, CA 94518, USA.

Abstract

Stem cells play a critical role in cancer development by contributing to cell heterogeneity, lineage plasticity, and drug resistance. We created gene expression networks from hundreds of mouse tissue samples (both normal and tumor) and integrated these with lineage tracing and single-cell RNA-seq, to identify convergence of cell states in premalignant tumor cells expressing markers of lineage plasticity and drug resistance. Two of these cell states representing multilineage plasticity or proliferation were inversely correlated, suggesting a mutually exclusive relationship. Treatment of carcinomas in vivo with chemotherapy repressed the proliferative state and activated multilineage plasticity whereas inhibition of differentiation repressed plasticity and potentiated responses to cell cycle inhibitors. Manipulation of this cell state transition point may provide a source of potential combinatorial targets for cancer therapy.

Publisher

American Association for the Advancement of Science (AAAS)

Cited by 1 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

1. Carcinogenesis at single-cell resolution;Nature Reviews Cancer;2024-07-04

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