Literature DB >> 20860760

The heme oxygenase system and oral diseases.

W Fan1, F Huang, X Zhu, D Li, S Fu, H He.   

Abstract

Oral Diseases (2011) 17, 252-257 Heme oxygenase (HO) system catabolizes heme into three products: carbon monoxide (CO), biliverdin/bilirubin and free iron, which consists of three forms identified to date: the oxidative stress-inducible protein HO-1 and the constitutive isozymes HO-2 and HO-3. HO has been involved in many physiological and pathophysiological processes, ranging from Alzheimer's disease to cancer. The interest in HO system by scientists and clinicians involved with the oral and maxillofacial region is fairly recent, and few papers currently cited on HO relate to diseases in this anatomical area. This review will focus on the current understanding of the physiological significance of HO-1 induction and its possible roles in the oral diseases studied to date. The implications for possible therapeutic manipulation of HO are also discussed.
© 2010 John Wiley & Sons A/S.

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Year:  2010        PMID: 20860760     DOI: 10.1111/j.1601-0825.2010.01732.x

Source DB:  PubMed          Journal:  Oral Dis        ISSN: 1354-523X            Impact factor:   3.511


  4 in total

Review 1.  Heme oxygenase-1 and gut ischemia/reperfusion injury: A short review.

Authors:  Yu-Feng Liao; Wei Zhu; Dong-Pei Li; Xiao Zhu
Journal:  World J Gastroenterol       Date:  2013-06-21       Impact factor: 5.742

2.  Elevation of HO-1 Expression Mitigates Intestinal Ischemia-Reperfusion Injury and Restores Tight Junction Function in a Rat Liver Transplantation Model.

Authors:  Xinjin Chi; Weifeng Yao; Hua Xia; Yi Jin; Xi Li; Jun Cai; Ziqing Hei
Journal:  Oxid Med Cell Longev       Date:  2015-05-10       Impact factor: 6.543

3.  Hydrogen-rich saline attenuates spinal cord hemisection-induced testicular injury in rats.

Authors:  Li Ge; Li-Hua Wei; Chang-Qing Du; Guo-Hua Song; Ya-Zhuo Xue; Hao-Shen Shi; Ming Yang; Xin-Xin Yin; Run-Ting Li; Xue-Er Wang; Zhen Wang; Wen-Gang Song
Journal:  Oncotarget       Date:  2017-06-27

4.  Chemoprevention of oxidative stress-associated oral carcinogenesis by sulforaphane depends on NRF2 and the isothiocyanate moiety.

Authors:  Aixian Lan; Wenjun Li; Yao Liu; Zhaohui Xiong; Xinyan Zhang; Shanshan Zhou; Olesya Palko; Hao Chen; Mayanga Kapita; Justin R Prigge; Edward E Schmidt; Xin Chen; Zheng Sun; Xiaoxin Luke Chen
Journal:  Oncotarget       Date:  2016-08-16
  4 in total

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