Angiogenesis in chronic liver disease and its complications
- PMID: 21073649
- DOI: 10.1111/j.1478-3231.2010.02369.x
Angiogenesis in chronic liver disease and its complications
Abstract
Nowadays, liver cancer, cirrhosis and other liver-related diseases are the fifth most common cause of mortality in the UK. Furthermore, chronic liver diseases (CLDs) are one of the major causes of death, which are still increasing year-on-year. Therefore, knowledge about the pathophysiology of CLDs and its complications is of uttermost importance. The goal of this review is to clarify the role of angiogenesis in the disease progression of various liver diseases. Looking closer at the pathophysiology of portal hypertension (PH), fibrosis, cirrhosis, non-alcoholic steatohepatitis (NASH) and hepatocellular carcinoma (HCC), we find that angiogenesis is a recurring factor in the disease progression. In PH, several factors involved in its pathogenesis, such as hypoxia, oxidative stress, inflammation and shear stress are potential mediators for the angiogenic response. The progression from fibrosis to cirrhosis, the end-point of CLDs, is distinguished by a prolonged inflammatory and fibrogenic process that leads to an abnormal angioarchitecture distinctive for cirrhosis. In several stages of NASH, a link might be made between the disease progression and hepatic microvasculature changes. HCC is one of the most vascular solid tumours in which angiogenesis plays an important role in its development, progression and metastasis. The close relationship between the progression of CLDs and angiogenesis emphasises the need for anti-angiogenic therapy as a tool for blocking or slowing down the disease progression. The fact that angiogenesis plays a pivotal role in CLDs gives rise to new opportunities for treating CLDs and its complications.
© 2010 John Wiley & Sons A/S.
Similar articles
-
Hypoxia: a link between fibrogenesis, angiogenesis, and carcinogenesis in liver disease.Semin Liver Dis. 2010 Aug;30(3):258-70. doi: 10.1055/s-0030-1255355. Epub 2010 Jul 21. Semin Liver Dis. 2010. PMID: 20665378 Review.
-
Angiogenesis in liver disease.J Hepatol. 2009 Mar;50(3):604-20. doi: 10.1016/j.jhep.2008.12.011. Epub 2008 Dec 31. J Hepatol. 2009. PMID: 19157625 Review.
-
Angiopoietins and Tie-2 expression in angiogenesis and proliferation of human hepatocellular carcinoma.Hepatology. 2003 May;37(5):1105-13. doi: 10.1053/jhep.2003.50204. Hepatology. 2003. PMID: 12717391
-
Angiogenesis in the progression from liver fibrosis to cirrhosis and hepatocelluar carcinoma.Expert Rev Gastroenterol Hepatol. 2021 Mar;15(3):217-233. doi: 10.1080/17474124.2021.1842732. Epub 2020 Nov 11. Expert Rev Gastroenterol Hepatol. 2021. PMID: 33131349 Review.
-
Vascular changes in hepatocellular carcinoma.Anat Rec (Hoboken). 2008 Jun;291(6):721-34. doi: 10.1002/ar.20668. Anat Rec (Hoboken). 2008. PMID: 18484619 Review.
Cited by
-
The role of fas/fas ligand system in the pathogenesis of liver cirrhosis and hepatocellular carcinoma.Hepat Mon. 2012 Nov;12(11):e6132. doi: 10.5812/hepatmon.6132. Epub 2012 Nov 3. Hepat Mon. 2012. PMID: 23300494 Free PMC article.
-
Role of the microenvironment in the pathogenesis and treatment of hepatocellular carcinoma.Gastroenterology. 2013 Mar;144(3):512-27. doi: 10.1053/j.gastro.2013.01.002. Epub 2013 Jan 9. Gastroenterology. 2013. PMID: 23313965 Free PMC article. Review.
-
Targeting Liver Sinusoidal Endothelial Cells: An Attractive Therapeutic Strategy to Control Inflammation in Nonalcoholic Fatty Liver Disease.Front Pharmacol. 2021 Apr 15;12:655557. doi: 10.3389/fphar.2021.655557. eCollection 2021. Front Pharmacol. 2021. PMID: 33935770 Free PMC article. Review.
-
Protective Effects of Flavone from Tamarix aphylla against CCl4-Induced Liver Injury in Mice Mediated by Suppression of Oxidative Stress, Apoptosis and Angiogenesis.Int J Mol Sci. 2019 Oct 21;20(20):5215. doi: 10.3390/ijms20205215. Int J Mol Sci. 2019. PMID: 31640181 Free PMC article.
-
Bevacizumab attenuates hepatic fibrosis in rats by inhibiting activation of hepatic stellate cells.PLoS One. 2013 Aug 30;8(8):e73492. doi: 10.1371/journal.pone.0073492. eCollection 2013. PLoS One. 2013. PMID: 24023685 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources
Medical