Growth characteristics of HCT116 xenografts lacking asparagine synthetase vary according to sex

Authors

Oladimeji Aladelokun, Department of Environmental Health Sciences, Yale School of Public Health, Yale University, New Haven, CT, USA.Follow
Lingeng Lu, Department of Chronic Disease Epidemiology, Yale School of Public Health, Yale University, New Haven, CT, 06510, USA.Follow
Jie Zheng, Department of Environmental Health Sciences, Yale School of Public Health, Yale University, New Haven, CT, USA.Follow
Hong Yan, Department of Environmental Health Sciences, Yale School of Public Health, Yale University, New Haven, CT, USA.Follow
Abhishek Jain, Department of Environmental Health Sciences, Yale School of Public Health, Yale University, New Haven, CT, USA.Follow
Joanna Gibson, Department of Pathology, Yale University, New Haven, CT, USA.
Sajid A. Khan, Division of Surgical Oncology, Department of Surgery, Yale School of Medicine, New Haven, CT, USA. sajid.khan@yale.edu.Follow
Caroline H. Johnson, Department of Environmental Health Sciences, Yale School of Public Health, Yale University, New Haven, CT, USA. caroline.johnson@yale.edu.Follow

Document Type

Article

Publication Title

Human genomics

Abstract

BACKGROUND: Sex-related differences in colorectal (CRC) incidence and mortality are well-documented. However, the impact of sex on metabolic pathways that drive cancer growth is not well understood. High expression of asparagine synthetase (ASNS) is associated with inferior survival for female CRC patients only. Here, we used a CRISPR/Cas9 technology to generate HCT116 ASNS and HCT 116 ASNS cancer cell lines. We examine the effects of ASNS deletion on tumor growth and the subsequent rewiring of metabolic pathways in male and female Rag2/IL2RG mice. RESULTS: ASNS loss reduces cancer burden in male and female tumor-bearing mice (40% reduction, q < 0.05), triggers metabolic reprogramming including gluconeogenesis, but confers a survival improvement (30 days median survival, q < 0.05) in female tumor-bearing mice alone. Transcriptomic analyses revealed upregulation of G-protein coupled estrogen receptor (GPER1) in tumors from male and female mice with HCT116 ASNS xenograft. Estradiol activates GPER1 in vitro in the presence of ASNS and suppresses tumor growth. CONCLUSIONS: Our study indicates that inferior survival for female CRC patients with high ASNS may be due to metabolic reprogramming that sustains tumor growth. These findings have translational relevance as ASNS/GPER1 signaling could be a future therapeutic target to improve the survival of female CRC patients.

First Page

67

DOI

10.1186/s40246-024-00635-3

Publication Date

6-17-2024

Recommended Citation

Aladelokun, Oladimeji; Lu, Lingeng; Zheng, Jie; Yan, Hong; Jain, Abhishek; Gibson, Joanna; Khan, Sajid A.; and Johnson, Caroline H., "Growth characteristics of HCT116 xenografts lacking asparagine synthetase vary according to sex" (2024). Surgery. 201.
https://scholar.bridgeporthospital.org/surgery/201

Identifier

38886847 (pubmed); PMC11184737 (pmc); 10.1186/s40246-024-00635-3 (doi); 10.1186/s40246-024-00635-3 (pii)