Loss of αl, 6‐fucosyltransferase inhibits chemical‐induced hepatocellular carcinoma and tumorigenesis by down‐regulating several cell signaling pathways. Issue 8 (14th April 2015)
- Record Type:
- Journal Article
- Title:
- Loss of αl, 6‐fucosyltransferase inhibits chemical‐induced hepatocellular carcinoma and tumorigenesis by down‐regulating several cell signaling pathways. Issue 8 (14th April 2015)
- Main Title:
- Loss of αl, 6‐fucosyltransferase inhibits chemical‐induced hepatocellular carcinoma and tumorigenesis by down‐regulating several cell signaling pathways
- Authors:
- Wang, Yuqin
Fukuda, Tomohiko
Isaji, Tomoya
Lu, Jishun
Im, Sanghun
Hang, Qinglei
Gu, Wei
Hou, Sicong
Ohtsubo, Kazuaki
Gu, Jianguo - Abstract:
- Abstract : Up‐regulation of core fucosylation catalyzed by α1, 6‐fucosyltransferase (Fut8) has been observed in hepatocellular carcinoma (HCC). Here, to explore the role of Fut8 expression in hepatocarcinogensis, we established the chemical‐induced HCC models in the male wild‐type (WT; Fut8 +/+ ), hetero ( Fut8 +/‐ ), and knockout (KO; mice by use of diethylnitrosamine (DEN) and pentobarbital (PB). In the Fut8 +/+ and Fut8 +/‐ mice, multiple large and vascularized nodules were induced with an increased expression of Fut8 after DEN and PB treatment. However, the formation of HCC in Fut8 ‐/‐ mice was suppressed almost completely. This potent inhibitory effect of Fut8 deficiency on tumorigenesis was also confirmed by the abolished tumor formation of Fnt8 KO human hepatoma cell line cells by use of a xenograft tumor model. Furthermore, loss of the Fut8 gene resulted in attenuated responses to epidermal growth factor (EGF) and hepatocyte growth factor (HGF) in the HepG2 cell line, which provides the possible mechanisms for the contribution of Fut8 to hepatocarcinogensis. Taken together, our study clearly demonstrated that core fucosylation acts as a critical functional modulator in the liver and implicated Fut8 as a prognostic marker, as well as a novel, therapeutic target for HCC.—Wang, Y., Fukuda, T., Isaji, T., Lu, J., Im, S., Hang, Q., Gu, W., Hou, S., Ohtsubo, K., Gu, J. Loss of α1, 6‐fucosyltransferase inhibits chemical induced hepatocellular carcinoma and tumorigenesis byAbstract : Up‐regulation of core fucosylation catalyzed by α1, 6‐fucosyltransferase (Fut8) has been observed in hepatocellular carcinoma (HCC). Here, to explore the role of Fut8 expression in hepatocarcinogensis, we established the chemical‐induced HCC models in the male wild‐type (WT; Fut8 +/+ ), hetero ( Fut8 +/‐ ), and knockout (KO; mice by use of diethylnitrosamine (DEN) and pentobarbital (PB). In the Fut8 +/+ and Fut8 +/‐ mice, multiple large and vascularized nodules were induced with an increased expression of Fut8 after DEN and PB treatment. However, the formation of HCC in Fut8 ‐/‐ mice was suppressed almost completely. This potent inhibitory effect of Fut8 deficiency on tumorigenesis was also confirmed by the abolished tumor formation of Fnt8 KO human hepatoma cell line cells by use of a xenograft tumor model. Furthermore, loss of the Fut8 gene resulted in attenuated responses to epidermal growth factor (EGF) and hepatocyte growth factor (HGF) in the HepG2 cell line, which provides the possible mechanisms for the contribution of Fut8 to hepatocarcinogensis. Taken together, our study clearly demonstrated that core fucosylation acts as a critical functional modulator in the liver and implicated Fut8 as a prognostic marker, as well as a novel, therapeutic target for HCC.—Wang, Y., Fukuda, T., Isaji, T., Lu, J., Im, S., Hang, Q., Gu, W., Hou, S., Ohtsubo, K., Gu, J. Loss of α1, 6‐fucosyltransferase inhibits chemical induced hepatocellular carcinoma and tumorigenesis by down‐regulating several cell signaling pathways. FASEB J. 29, 3217‐3227 (2015). www.fasebj.org … (more)
- Is Part Of:
- FASEB journal. Volume 29:Issue 8(2015)
- Journal:
- FASEB journal
- Issue:
- Volume 29:Issue 8(2015)
- Issue Display:
- Volume 29, Issue 8 (2015)
- Year:
- 2015
- Volume:
- 29
- Issue:
- 8
- Issue Sort Value:
- 2015-0029-0008-0000
- Page Start:
- 3217
- Page End:
- 3227
- Publication Date:
- 2015-04-14
- Subjects:
- N‐glycosykition -- glycosyltransferase -- cell proliferation
Biology -- Periodicals
Biology, Experimental -- Periodicals
570 - Journal URLs:
- http://onlinelibrary.wiley.com/ ↗
- DOI:
- 10.1096/fj.15-270710 ↗
- Languages:
- English
- ISSNs:
- 0892-6638
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 13227.xml