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Peripheral-dominant liver fibrosis and tumor distribution in a mouse model of congestive hepatopathy.
Kawai, Hironari; Osawa, Yosuke; Tsunoda, Tomoyuki; Matsuda, Michitaka; Okawara, Miku; Sakamoto, Yuzuru; Shimagaki, Tomonari; Tsutsui, Yuriko; Yoshida, Yuichi; Yoshikawa, Shiori; Doi, Hiroyoshi; Mori, Taizo; Yamazoe, Taiji; Yoshio, Sachiyo; Okamura, Tadashi; Sugiyama, Masaya; Okuzaki, Daisuke; Komatsu, Haruki; Inui, Ayano; Yanaga, Katsuhiko; Ikegami, Toru; Kanto, Tatsuya.
Affiliation
  • Kawai H; The Research Center for Hepatitis and Immunology, National Center for Global Health and Medicine, Ichikawa, Chiba, Japan.
  • Osawa Y; Department of Surgery, The Jikei University School of Medicine, Minato-ku, Tokyo, Japan.
  • Tsunoda T; The Research Center for Hepatitis and Immunology, National Center for Global Health and Medicine, Ichikawa, Chiba, Japan.
  • Matsuda M; Department of Gastroenterology, International University of Health and Welfare Hospital, Nasushiobara, Tochigi, Japan.
  • Okawara M; Department of Pediatric Hepatology and Gastroenterology, Saiseikai Yokohama-shi Tobu Hospital, Yokohama, Kanagawa, Japan.
  • Sakamoto Y; The Research Center for Hepatitis and Immunology, National Center for Global Health and Medicine, Ichikawa, Chiba, Japan.
  • Shimagaki T; Karsh Division of Gastroenterology and Hepatology, Department of Medicine, Cedars-Sinai Medical Center, Los Angeles, California, USA.
  • Tsutsui Y; The Research Center for Hepatitis and Immunology, National Center for Global Health and Medicine, Ichikawa, Chiba, Japan.
  • Yoshida Y; The Research Center for Hepatitis and Immunology, National Center for Global Health and Medicine, Ichikawa, Chiba, Japan.
  • Yoshikawa S; The Research Center for Hepatitis and Immunology, National Center for Global Health and Medicine, Ichikawa, Chiba, Japan.
  • Doi H; The Research Center for Hepatitis and Immunology, National Center for Global Health and Medicine, Ichikawa, Chiba, Japan.
  • Mori T; The Research Center for Hepatitis and Immunology, National Center for Global Health and Medicine, Ichikawa, Chiba, Japan.
  • Yamazoe T; The Research Center for Hepatitis and Immunology, National Center for Global Health and Medicine, Ichikawa, Chiba, Japan.
  • Yoshio S; The Research Center for Hepatitis and Immunology, National Center for Global Health and Medicine, Ichikawa, Chiba, Japan.
  • Okamura T; The Research Center for Hepatitis and Immunology, National Center for Global Health and Medicine, Ichikawa, Chiba, Japan.
  • Sugiyama M; The Research Center for Hepatitis and Immunology, National Center for Global Health and Medicine, Ichikawa, Chiba, Japan.
  • Okuzaki D; The Research Center for Hepatitis and Immunology, National Center for Global Health and Medicine, Ichikawa, Chiba, Japan.
  • Komatsu H; Department of Laboratory Animal Medicine, Research Institute, National Center for Global Health and Medicine, Shinjuku, Tokyo, Japan.
  • Inui A; Genome Medical Sciences Project, National Center for Global Health and Medicine, Ichikawa, Chiba, Japan.
  • Yanaga K; Genome information Research Center, Research Institute for Microbial Disease, Osaka University, Suita, Osaka, Japan.
  • Ikegami T; Department of Pediatrics, Toho University Medical Center, Sakura Hospital, Sakura, Chiba, Japan.
  • Kanto T; Department of Pediatric Hepatology and Gastroenterology, Saiseikai Yokohama-shi Tobu Hospital, Yokohama, Kanagawa, Japan.
Hepatol Res ; 53(4): 370-376, 2023 Apr.
Article in En | MEDLINE | ID: mdl-36461886
ABSTRACT

AIM:

Congestive hepatopathy often leads to liver fibrosis and hepatocellular carcinoma. Imaging modalities provided clinical evidence that elevation of liver stiffness and tumor occurrence are mainly induced in the periphery of the liver in patients with congestive hepatopathy. However, clinical relevance of liver stiffness and liver fibrosis is unclear because liver congestion itself increases liver stiffness in congestive hepatopathy. It also unclear which factors configure such regional disparity of tumor development in patients with congestive hepatopathy. To answer these questions, we evaluated the macroscopic spatial distribution of liver fibrosis and tumors in the murine model of congestive hepatopathy.

METHODS:

Chronic liver congestion was induced by partial ligation of the suprahepatic inferior vena cava. Distribution of liver congestion, fibrosis, and tumors in partial ligation of the suprahepatic inferior vena cava mice were assessed by histological findings, laser microdissection (LMD)-based qPCR and enhanced computed tomography. LMD-based RNA-sequencing was performed to identify causal factors that promote tumor development in congestive hepatopathy.

RESULTS:

Liver fibrosis was mainly induced in the periphery of the liver and co-localized with distribution of liver congestion. Liver tumors were also induced in the periphery of the liver where liver congestion and fibrosis occurred. LMD-based RNA-sequencing revealed the upregulation of extracellular matrix/collagen fibril-, wound healing-, angiogenesis-, morphogenesis-, and cell motility-related signaling pathways in periphery of liver compared with liver center.

CONCLUSIONS:

Our findings showed the experimental relevance of liver congestion, fibrosis, and tumor development in congestive hepatopathy, and may provide important locational information. Macroscopic regional disparity observed in this murine model should be considered to manage patients with congestive hepatopathy.
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Type of study: Prognostic_studies Language: En Journal: Hepatol Res Year: 2023 Document type: Article Affiliation country: Japan

Full text: 1 Collection: 01-internacional Database: MEDLINE Type of study: Prognostic_studies Language: En Journal: Hepatol Res Year: 2023 Document type: Article Affiliation country: Japan