Fibrosis, regeneration and cancer: what is the link?
- PMID: 22102616
- DOI: 10.1093/ndt/gfr567
Fibrosis, regeneration and cancer: what is the link?
Abstract
Tubulo-interstitial fibrosis constitutes the final common pathway for all pathological conditions that evolve towards chronic kidney disease, and transforming growth factor-β1 plays a key role in this process. Furthermore, neutrophil gelatinase-associated lipocalin appears not only to be a simple marker of renal injury but also an active player in disease progression. We are not yet able to control and modulate this phenomenon. Therefore, a better understanding of fibrogenic molecular mechanisms is necessary to detect possible therapeutic strategies that interfere with fibrosis and then stop the progression of renal disease. The line of research called 'regenerative medicine' works toward this. According to many authors, the formation of a fibrotic extracellular matrix disrupts the cells' polarity and stimulates their proliferation, creating conditions for cancer development. However, there is another plausible hypothesis: is it possible that fibrosis provides a sort of 'protection' from the development of a cancer as a consequence of the intense proliferation that characterizes any inflammatory process? In superior organisms, and also in humans, regeneration may have been selected negatively and replaced by fibrosis in the course of evolution, to warrant species survival: in fact, unchecked pluripotent cell production and proliferation can lead to tumour development and the potential death of a single individual. Hence, tumours might be the outcome of the failure of fibrotic processes, most likely due to some mediators predominating over others. So, valid experimental models are necessary to understand the interactions that exist between fibrosis and tumours and to evaluate the real advantage of therapies that aim to inhibit the fibrotic process at the renal level or that of other organs. The ideal approach would be to limit fibrosis and then organ function loss but without exposing the patient to risks of developing a tumour, starting from as early as the drugs prescribed.
Similar articles
-
[Regeneration following acute kidney damage].Verh K Acad Geneeskd Belg. 1998;60(4):359-83; discussion 383-4. Verh K Acad Geneeskd Belg. 1998. PMID: 9883082 Dutch.
-
Liver fibrosis: from the bench to clinical targets.Dig Liver Dis. 2004 Apr;36(4):231-42. doi: 10.1016/j.dld.2004.01.003. Dig Liver Dis. 2004. PMID: 15115333 Review.
-
Cytokines in epithelial-mesenchymal transition: a new insight into obstructive nephropathy.J Urol. 2008 Aug;180(2):461-8. doi: 10.1016/j.juro.2008.04.001. Epub 2008 Jun 11. J Urol. 2008. PMID: 18550128 Review.
-
Progression in chronic kidney disease.Adv Chronic Kidney Dis. 2005 Oct;12(4):353-65. doi: 10.1053/j.ackd.2005.07.011. Adv Chronic Kidney Dis. 2005. PMID: 16198274 Review.
-
Direct contribution of epithelium to organ fibrosis: epithelial-mesenchymal transition.Hum Pathol. 2009 Oct;40(10):1365-76. doi: 10.1016/j.humpath.2009.02.020. Epub 2009 Aug 19. Hum Pathol. 2009. PMID: 19695676 Review.
Cited by
-
Role of the Hippo Pathway in Fibrosis and Cancer.Cells. 2019 May 16;8(5):468. doi: 10.3390/cells8050468. Cells. 2019. PMID: 31100975 Free PMC article. Review.
-
c-Rel orchestrates energy-dependent epithelial and macrophage reprogramming in fibrosis.Nat Metab. 2020 Nov;2(11):1350-1367. doi: 10.1038/s42255-020-00306-2. Epub 2020 Nov 9. Nat Metab. 2020. PMID: 33168981 Free PMC article.
-
Levels of 8-OxodG Predict Hepatobiliary Pathology in Opisthorchis viverrini Endemic Settings in Thailand.PLoS Negl Trop Dis. 2015 Jul 31;9(7):e0003949. doi: 10.1371/journal.pntd.0003949. eCollection 2015. PLoS Negl Trop Dis. 2015. PMID: 26230769 Free PMC article.
-
Growth Factors in Regeneration and Regenerative Medicine: "the Cure and the Cause".Front Endocrinol (Lausanne). 2020 Jul 7;11:384. doi: 10.3389/fendo.2020.00384. eCollection 2020. Front Endocrinol (Lausanne). 2020. PMID: 32733378 Free PMC article. Review.
-
Renoprotective effect of erythropoietin in zebrafish after administration of gentamicin: an immunohistochemical study for β-catenin and c-kit expression.J Nephrol. 2017 Jun;30(3):385-391. doi: 10.1007/s40620-016-0353-y. Epub 2016 Sep 27. J Nephrol. 2017. PMID: 27679401
Publication types
MeSH terms
LinkOut - more resources
Full Text Sources
Medical