C3 NASH und die metabolische Wirkung von IL-6 bei der hepatozellulären Karzinogenese
Prof. Eithan Galun, M.D.
Director, Goldyne Savad Institute of Gene Therapy
Hadassah Hebrew University Hospital
Weitere beteiligte Mitarbeiter:
Tali Lanton (Post-doc)
Mor Levy (PhD student)
Marion Richardson (Fund Administration)
C3 in 60 SekundenVideoarchivonline seit 02.11.2012
Aktuelles aus der Arbeitsgruppe:
Lanton T, Shriki A, Nechemia-Arbely Y, Abramovitch R, Levkovitch O, Adar R, Rosenberg N, Paldor M, Goldenberg D, Sonnenblick A, Peled A, Rose John S, Galun E, Axelrod JH
Interleukin 6-dependent genomic instability heralds accelerated carcinogenesis following liver regeneration on a background of chronic hepatitis
Hepatology. 2017 May;65(5):1600-1611. doi: 10.1002/hep.29004. Epub 2017 Mar 23
Rivkin M, Simerzin A, Zorde-Khvalevsky E, Chai C, Yuval JB, Rosenberg N, Harari-Steinfeld R, Schneider R, Amir G, Condiotti R, Heikenwalder M, Weber A, Schramm C, Wege H, Kluwe J, Galun E, Giladi H
Inflammation-Induced Expression and Secretion of MicroRNA 122 Leads to Reduced Blood Levels of Kidney-derived Erythropoietin and Anemia
Gastroenterology. 2016 Jul 28. pii:S0016-5085(16)34827-2. doi: 10.1053/j.gastro.2016.07.031. [Epub ahead of print]
Liver inflammation and cancer: The role of tissue microenvironment in generating the tumor-promoting niche (TPN) in the development of hepatocellular carcinoma
Hepatology. 2016 Feb;63(2):354-6. doi: 10.1002/hep.28344. Epub 2015 Dec 18.
Simerzin A, Zorde-Khvalevsky E, Rivkin M, Adar R, Zucman-Rossi J, Couchy G, Roskams T, Govaere O, Oren M, Giladi H, Galun E
The liver-specific microRNA-122*, the complementary strand of microRNA-122, acts as a tumor suppressor by modulating the p53/mouse double minute 2 homolog circuitry
Hepatology. 2016 Jun 15. doi: 10.1002/hep.28679. [Epub ahead of print]
The mechanism how NASH causes HCC is unknown. We and others show that IL-6 depletion causes liver steatosis and potentiates inflammation; on the other hand, IL-6 induces HCC in mice following administration of carcinogens. We wish to elucidate whether IL-6 plays a protective role against chronic liver injury associated with NAFLD, preventing HCC. Specifically, we wish: 1) to understand the potential role of the IL-6 pathway (signaling and transsignaling) in HCC development; 2) to determine the impact of diet-induced NAFLD on the IL-6 pathway in hepatocarcinogenesis; and 3) to assess novel therapeutic avenues to target IL-6 and/or IL-6 in obesity-driven HCC.
In the first funding period, we have investigated the role of the H19 non-coding RNA imprinting gene in liver cancer development. Our results are quite surprising: We had found that H19 is actually a pluripotent factor which controls both Nanog and Oct4. In embryos and induced pluripotent stem cells, Nanog, together with other factors such as Oct4, sets the ground state of pluripotency. The reduction of H19 levels in our human embryonic carcinoma cells is associated with early differentiation, and the reduction of pluripotent markers. Interestingly, in the mouse model, the Mdr2-IL-6 double KO mice, H19 is very significantly increased. We are currently investigating the molecular mechanism behind this observation as it possibly explains the increase in hepatocarcinogenesis.