Compression drives diverse transcriptomic and phenotypic adaptations in melanoma

Author:

Zhang Xingjian12ORCID,Shi Xin3ORCID,Zhang Dingyao1,Gong Xiangyu1,Wen Zhang1,Demandel Israel1ORCID,Zhang Junqi1ORCID,Rossello-Martinez Alejandro1,Chan Trevor J.4,Mak Michael12ORCID

Affiliation:

1. Department of Biomedical Engineering, Yale University, New Haven, CT 06511

2. Yale Cancer Center, Yale University, New Haven, CT 06511

3. School of Chemical Engineering and Technology, Tianjin University, Tianjin 300350, China

4. Department of Bioengineering, University of Pennsylvania, Philadelphia, PA 19104

Abstract

Physical forces are prominent during tumor progression. However, it is still unclear how they impact and drive the diverse phenotypes found in cancer. Here, we apply an integrative approach to investigate the impact of compression on melanoma cells. We apply bioinformatics to screen for the most significant compression-induced transcriptomic changes and investigate phenotypic responses. We show that compression-induced transcriptomic changes are associated with both improvement and worsening of patient prognoses. Phenotypically, volumetric compression inhibits cell proliferation and cell migration. It also induces organelle stress and intracellular oxidative stress and increases pigmentation in malignant melanoma cells and normal human melanocytes. Finally, cells that have undergone compression become more resistant to cisplatin treatment. Our findings indicate that volumetric compression is a double-edged sword for melanoma progression and drives tumor evolution.

Funder

HHS | National Institutes of Health

Publisher

Proceedings of the National Academy of Sciences

Subject

Multidisciplinary

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