Epithelial‐mesenchymal transition polarization in ovarian carcinomas from patients with high social isolation

Susan K. Lutgendorf & Anil K. Sood · 2020-07-21

Background

Social isolation has shown robust associations with clinical outcomes in the general population and in patients with cancer. In patients with ovarian cancer, social isolation has been found to be related to decreased survival and multiple biomarkers supporting tumor progression. However, to the authors' knowledge, little is known regarding the relationship between social isolation and the molecular characteristics of ovarian tumors. Herein, the authors have used genome‐wide transcriptional profiling to quantify associations between social isolation and epithelial‐mesenchymal transition (EMT) polarization in ovarian tumors and transcriptome‐driven, promoter‐based bioinformatics analyses to identify gene regulatory pathways that may potentially underlie these changes.

Methods

Tumor was sampled during primary surgical resection and immediately frozen in liquid nitrogen. After RNA extraction, microarray analysis of the transcriptome was performed and samples were analyzed to assess associations between EMT‐related gene transcripts and social isolation (as indicated by a Social Provisions Scale Attachment subscale score <15). Convergent validation was provided by a promoter‐based bioinformatic analysis of transcription factor activity.

Results

Primary analyses of 99 women demonstrated a lower average expression of gene transcripts previously associated with epithelial differentiation in women with high social isolation (−0.143 ± 0.048 log2 mRNA abundance; P = .004), but no difference in mesenchymal differentiation as a function of social isolation (+0.007 ± 0.0064 log2 mRNA abundance; P = .900). Upregulated activity was shown for 3 of the 4 targeted EMT‐related transcription factors, including GATA4 (P = .014); SMAD2, SMAD3, and/or SMAD4 (P < .001); and TWIST1 (P < .001). Analyses of SNAIL2/SLUG activity indicated a directional trend toward increased activity that did not reach statistical significance (P = .123).

Conclusions

The findings of the current study demonstrated differential EMT polarization and EMT‐related transcription factor activity according to social isolation, a known socioenvironmental risk factor.

Lay Summary

  • Social isolation has shown robust associations with clinical outcomes in the general population and in patients with cancer. Herein, the authors examined the relationship between social isolation and the molecular characteristics of ovarian tumors.

  • The authors investigated the epithelial‐mesenchymal transition (EMT), a process whereby tumor cells lose epithelial characteristics and become more embryonic (mesenchymal), thereby enhancing invasiveness.

  • Primary analyses demonstrated lower expression of genes previously associated with epithelial differentiation and increased activity of specific EMT‐related transcription factors in individuals with high social isolation, indicating increased EMT polarization in these patients. These findings extend the understanding of how socioenvironmental factors may modulate tumor growth.

Journal
Cancer
Funding
Behavioral Influences on Ovarian Cancer Progression: Role of ChemoresistanceHarnessing the power of exosomes for non-coding RNA deliveryCancer Center Support GrantLiving Well: A Web-based Intervention to Improve Quality of Life in Rural and Urban Ovarian Cancer SurvivorsNeural, Inflammatory, and Genomic Mechanisms Underlying Risk for Depression in AdolescenceCore B - Program Development Pilot CoreOvarian Cancer: Mechanisms of Neuroendocrine RegulationBiobehavioral Influences and the Ovarian Tumor MicroenvironmentHarnessing the power of exosomes for non-coding RNA deliveryCancer Center Support GrantOvarian Cancer: Mechanisms of Neuroendocrine RegulationBiobehavioral Influences and the Ovarian Tumor MicroenvironmentBehavioral Influences on Ovarian Cancer Progression: Role of ChemoresistanceLiving Well: A Web-based Intervention to Improve Quality of Life in Rural and Urban Ovarian Cancer SurvivorsSocial regulation of pro-inflammatory monocytesNIA NIH HHS Grant AG17265Social regulation of pro-inflammatory monocytesNational Institute on Aging Grant AG043404National Institute on Aging Grant AG17265National Cancer Institute Grant CA109298National Cancer Institute Grant CA140933National Cancer Institute Grant CA193249National Cancer Institute Grant CA209904National Cancer Institute Grant CA246540Cancer Center Support Grant

NCI NIH HHS

R35 CA209904

NCI NIH HHS

P30CA086862

NIMH NIH HHS

K08 MH103443

NIA NIH HHS

P30 AG017265

NCI NIH HHS

R01 CA140933

NCI NIH HHS

P30 CA086862

NCI NIH HHS

R01 CA109298

NCI NIH HHS

R01 CA193249

NCI NIH HHS

R01 CA246540

NIA NIH HHS

R01 AG043404

National Cancer Institute

P30CA086862