Kidney injury molecule-1 inhibits metastasis of renal cell carcinoma
Abstract Metastasis is present in approximately 30% of patients diagnosed with renal cell carcinoma (RCC) and is associated with a 5-year survival rate of < 15%. Kidney injury molecule 1 (KIM-1), encoded by the HAVCR1 gene, is a proximal tubule cell-surface glycoprotein and a biomarker for early...
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2021-06-01
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Online Access: | https://doi.org/10.1038/s41598-021-90919-8 |
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doaj-3782d411acd84457baceedd045480f732021-06-06T11:37:00ZengNature Publishing GroupScientific Reports2045-23222021-06-0111111210.1038/s41598-021-90919-8Kidney injury molecule-1 inhibits metastasis of renal cell carcinomaJasper C. Lee0Demitra M. Yotis1Ji Yun Lee2Marie A. Sarabusky3Bradly Shrum4Audrey Champagne5Ola Z. Ismail6Elena Tutunea-Fatan7Hon S. Leong8Lakshman Gunaratnam9Department of Microbiology and Immunology, Schulich School of Medicine and Dentistry, Western UniversityDepartment of Microbiology and Immunology, Schulich School of Medicine and Dentistry, Western UniversityDepartment of Microbiology and Immunology, Schulich School of Medicine and Dentistry, Western UniversityDepartment of Microbiology and Immunology, Schulich School of Medicine and Dentistry, Western UniversityMatthew Mailing Centre for Translational Transplant Studies, Lawson Health Research InstituteCentre de recherche du CHU de Québec-Université Laval, CHU de Québec-Université LavalDepartment of Microbiology and Immunology, Schulich School of Medicine and Dentistry, Western UniversityMatthew Mailing Centre for Translational Transplant Studies, Lawson Health Research InstituteSunnybrook Health Sciences CentreDepartment of Microbiology and Immunology, Schulich School of Medicine and Dentistry, Western UniversityAbstract Metastasis is present in approximately 30% of patients diagnosed with renal cell carcinoma (RCC) and is associated with a 5-year survival rate of < 15%. Kidney injury molecule 1 (KIM-1), encoded by the HAVCR1 gene, is a proximal tubule cell-surface glycoprotein and a biomarker for early detection of RCC, but its pathophysiological significance in RCC remains unclear. We generated human and murine RCC cell lines either expressing or lacking KIM-1, respectively, and compared their growth and metastatic properties using validated methods. Surprisingly, KIM-1 expression had no effect on cell proliferation or subcutaneous tumour growth in immune deficient (Rag1−/−) Balb/c mice, but inhibited cell invasion and formation of lung metastasis in the same model. Further, we show that the inhibitory effect of KIM-1 on metastases was observed in both immune deficient and immune competent mice. Transcriptomic profiling identified the mRNA for the pro-metastatic GTPase, Rab27b, to be downregulated significantly in KIM-1 expressing human and murine RCC cells. Finally, analysis of The Cancer Genome Atlas (TCGA) data revealed that elevated HAVCR1 mRNA expression in the two most common types of RCC, clear cell and papillary RCC, tumours correlated with significantly improved overall patient survival. Our findings reveal a novel role for KIM-1 in inhibiting metastasis of RCC and suggests that tumour-associated KIM-1 expression may be a favourable prognostic factor.https://doi.org/10.1038/s41598-021-90919-8 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Jasper C. Lee Demitra M. Yotis Ji Yun Lee Marie A. Sarabusky Bradly Shrum Audrey Champagne Ola Z. Ismail Elena Tutunea-Fatan Hon S. Leong Lakshman Gunaratnam |
spellingShingle |
Jasper C. Lee Demitra M. Yotis Ji Yun Lee Marie A. Sarabusky Bradly Shrum Audrey Champagne Ola Z. Ismail Elena Tutunea-Fatan Hon S. Leong Lakshman Gunaratnam Kidney injury molecule-1 inhibits metastasis of renal cell carcinoma Scientific Reports |
author_facet |
Jasper C. Lee Demitra M. Yotis Ji Yun Lee Marie A. Sarabusky Bradly Shrum Audrey Champagne Ola Z. Ismail Elena Tutunea-Fatan Hon S. Leong Lakshman Gunaratnam |
author_sort |
Jasper C. Lee |
title |
Kidney injury molecule-1 inhibits metastasis of renal cell carcinoma |
title_short |
Kidney injury molecule-1 inhibits metastasis of renal cell carcinoma |
title_full |
Kidney injury molecule-1 inhibits metastasis of renal cell carcinoma |
title_fullStr |
Kidney injury molecule-1 inhibits metastasis of renal cell carcinoma |
title_full_unstemmed |
Kidney injury molecule-1 inhibits metastasis of renal cell carcinoma |
title_sort |
kidney injury molecule-1 inhibits metastasis of renal cell carcinoma |
publisher |
Nature Publishing Group |
series |
Scientific Reports |
issn |
2045-2322 |
publishDate |
2021-06-01 |
description |
Abstract Metastasis is present in approximately 30% of patients diagnosed with renal cell carcinoma (RCC) and is associated with a 5-year survival rate of < 15%. Kidney injury molecule 1 (KIM-1), encoded by the HAVCR1 gene, is a proximal tubule cell-surface glycoprotein and a biomarker for early detection of RCC, but its pathophysiological significance in RCC remains unclear. We generated human and murine RCC cell lines either expressing or lacking KIM-1, respectively, and compared their growth and metastatic properties using validated methods. Surprisingly, KIM-1 expression had no effect on cell proliferation or subcutaneous tumour growth in immune deficient (Rag1−/−) Balb/c mice, but inhibited cell invasion and formation of lung metastasis in the same model. Further, we show that the inhibitory effect of KIM-1 on metastases was observed in both immune deficient and immune competent mice. Transcriptomic profiling identified the mRNA for the pro-metastatic GTPase, Rab27b, to be downregulated significantly in KIM-1 expressing human and murine RCC cells. Finally, analysis of The Cancer Genome Atlas (TCGA) data revealed that elevated HAVCR1 mRNA expression in the two most common types of RCC, clear cell and papillary RCC, tumours correlated with significantly improved overall patient survival. Our findings reveal a novel role for KIM-1 in inhibiting metastasis of RCC and suggests that tumour-associated KIM-1 expression may be a favourable prognostic factor. |
url |
https://doi.org/10.1038/s41598-021-90919-8 |
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