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Current
Gene Therapy
ISSN: 1566-5232


Cytoglobin: A Novel Potential Gene Medicine for Fibrosis
and Cancer Therapy
Yinghui Lv, Qizhao Wang, Yong Diao and Ruian
Xu*
[Abstract]
Abstracts

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Cytoglobin: A Novel Potential Gene Medicine for
Fibrosis and Cancer Therapy
Yinghui Lv, Qizhao Wang, Yong Diao and Ruian
Xu*
Attempts have been made by conventional gene therapy
to suppress hepatic fibrogenesis, but potential oncogenic
activity may prevent its clinical use. Recently, a novel major
approach has been developed for resolution of liver fibrosis
and cirrhosis: inactivation of hepatic stellate cells (HSC)
using the endogenous expressing gene, which could mediate
the homeostatic adaptation of liver. Cytoglobin (Cygb), originally
identified in cultured rat HSC, is in a new class of heme
containing proteins known as the hexacoordinate globin superfamily.
These proteins exhibit peroxidase activity against hydrogen
peroxides and lipid hydroperoxides. Considerable attention
has been focused on the potential benefits of use of Cygb
in fibrosis therapy, as up-regulation of Cygb expression could
reduce oxidant stress, suppress HSC differentiation to a myofibroblast-like
phenotype and eventually prevent the progress of liver fibrosis.
Cygb has also been found to be a candidate tumor suppressor
gene that might provide a new option for cancer gene therapy.
In this review we systematically analyze the potential of
Cygb as a prospective gene medicine for curing fibrosis, cancer,
and other diseases such as diabetes. The molecular structure,
regulation and subcellular location of Cygb are reviewed as
well.
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