Hepatic lipids promote liver metastasis

Bibliographic Details
Title: Hepatic lipids promote liver metastasis
Authors: Yongjia Li, Xinming Su, Nidhi Rohatgi, Yan Zhang, Jonathan R. Brestoff, Kooresh I. Shoghi, Yalin Xu, Clay F. Semenkovich, Charles A. Harris, Lindsay L. Peterson, Katherine N. Weilbaecher, Steven L. Teitelbaum, Wei Zou
Source: JCI Insight, Vol 5, Iss 17 (2020)
Publisher Information: American Society for Clinical investigation, 2020.
Publication Year: 2020
Collection: LCC:Medicine
Subject Terms: Hepatology, Oncology, Medicine
More Details: Obesity predisposes to cancer and a virtual universality of nonalcoholic fatty liver disease (NAFLD). However, the impact of hepatic steatosis on liver metastasis is enigmatic. We find that while control mice were relatively resistant to hepatic metastasis, those which were lipodystrophic or obese, with NAFLD, had a dramatic increase in breast cancer and melanoma liver metastases. NAFLD promotes liver metastasis by reciprocal activation initiated by tumor-induced triglyceride lipolysis in juxtaposed hepatocytes. The lipolytic products are transferred to cancer cells via fatty acid transporter protein 1, where they are metabolized by mitochondrial oxidation to promote tumor growth. The histology of human liver metastasis indicated the same occurs in humans. Furthermore, comparison of isolates of normal and fatty liver established that steatotic lipids had enhanced tumor-stimulating capacity. Normalization of glucose metabolism by metformin did not reduce steatosis-induced metastasis, establishing the process is not mediated by the metabolic syndrome. Alternatively, eradication of NAFLD in lipodystrophic mice by adipose tissue transplantation reduced breast cancer metastasis to that of control mice, indicating the steatosis-induced predisposition is reversible.
Document Type: article
File Description: electronic resource
Language: English
ISSN: 2379-3708
Relation: https://doaj.org/toc/2379-3708
DOI: 10.1172/jci.insight.136215
Access URL: https://doaj.org/article/823957cb09a84ffc8fbd4f0dac29a9b4
Accession Number: edsdoj.823957cb09a84ffc8fbd4f0dac29a9b4
Database: Directory of Open Access Journals
More Details
ISSN:23793708
DOI:10.1172/jci.insight.136215
Published in:JCI Insight
Language:English