Sexual dimorphism of liver metastasis by murine pancreatic neuroendocrine tumors is affected by expression of complement C5 Journal Article


Authors: Contractor, T.; Kobayashi, S.; da Silva, E.; Clausen, R.; Chan, C.; Vosburgh, E.; Tang, L. H.; Levine, A. J.; Harris, C. R.
Article Title: Sexual dimorphism of liver metastasis by murine pancreatic neuroendocrine tumors is affected by expression of complement C5
Abstract: In a mouse model for neuroendocrine tumors of the pancreas (PanNETs), liver metastasis occurred at a higher frequency in males. Male mice also had higher serum and intratumoral levels of the innate immunity protein complement C5. In mice that lost the ability to express complement C5, there was a lower frequency of metastasis, and males no longer had a higher frequency of metastasis than females. Treatment with PMX53, a small molecule antagonist of C5aR1/CD88, the receptor for complement C5a, also reduced metastasis. Mice lacking a functional gene for complement C5 had smaller primary tumors, which were less invasive and lacked the CD68+ macrophages that have previously been associated with metastasis in this type of tumor. This is the first report of a gene that causes sexual dimorphism of metastasis in a mouse model. In the human disease, which also shows sexual dimorphism for metastasis, clinically advanced tumors expressed more complement C5 than less advanced tumors.
Keywords: metastasis; pancreatic; neuroendocrine tumors; complement c5; sexual dimorphism
Journal Title: Oncotarget
Volume: 7
Issue: 21
ISSN: 1949-2553
Publisher: Impact Journals  
Date Published: 2016-05-24
Start Page: 30585
End Page: 30596
Language: English
DOI: 10.18632/oncotarget.8874
PROVIDER: scopus
PUBMED: 27105526
PMCID: PMC5058703
DOI/URL:
Notes: Article -- Export Date: 1 July 2016 -- Source: Scopus
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  1. Laura Hong Tang
    447 Tang