Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
8
pubmed:dateCreated
2008-7-21
pubmed:abstractText
Ogg1 DNA repair enzyme recognizes and excises oxidative stress-caused 8-hydroxyl-deoxyguanosine (8-OHdG) from GC base-pairs. Ogg1 knockout mice are phenotypically normal, but exhibit elevated levels of 8-OHdG in nuclear and mitochondrial DNA, as well as moderately elevated mutagenesis and spontaneous lung tumors and UV-induced skin tumors. To elucidate the mechanistic role of inflammation-caused oxidative stress in carcinogenesis, the development of chronic ulcerative colitis (UC)-induced carcinoma in Ogg1 knockout mice was studied using a dextran sulfate sodium (DSS)-induced UC model without the use of a carcinogen. Ogg1 (-/-), Ogg1 (+/-), and wild type C57BL/6 mice were subjected to long-term, cyclic DSS treatment to induce chronic UC and carcinogenesis. In wild type C57BL/6 control mice after 15 cycles of DSS treatment, colorectal adenocarcinoma incidence was 24.1% (7/29 mice), with a tumor volume of 27.9 +/- 5.2 mm(3). Ogg1 (-/-) mice showed significantly increased adenocarcinoma development in the colon with a tumor incidence of 57.1% (12 of 21 mice, P < 0.05) and a tumor volume of 35.1 +/- 6.1 mm(3). Ogg1 mice (+/-) also exhibited significantly increased tumor development in the colon with a tumor incidence of 50.0% (13/26 mice) and a tumor volume of 29.1 +/- 7.2 mm(3). Histopathologic analyses revealed that colorectal tumors were well-differentiated tubular adenocarcinomas or mucinous carcinoma and adjacent colonic mucosa showed mild to moderate chronic UC. Using immunohistochemical approaches, Ogg1 (-/-) and (+/-) mice exhibited similar numbers and staining intensities of macrophages in UC areas as seen in Ogg1 (+/+) mice, but markedly increased numbers and staining intensities of 8-OHdG positive inflammatory and epithelial cells. These results provide important evidence on the relationship between inflammation-caused oxidative stress, DNA repair enzyme Ogg1, and carcinogenesis.
pubmed:grant
pubmed:commentsCorrections
http://linkedlifedata.com/resource/pubmed/commentcorrection/18300266-10557315, http://linkedlifedata.com/resource/pubmed/commentcorrection/18300266-10753213, http://linkedlifedata.com/resource/pubmed/commentcorrection/18300266-11454679, http://linkedlifedata.com/resource/pubmed/commentcorrection/18300266-11532032, http://linkedlifedata.com/resource/pubmed/commentcorrection/18300266-11532868, http://linkedlifedata.com/resource/pubmed/commentcorrection/18300266-11554297, http://linkedlifedata.com/resource/pubmed/commentcorrection/18300266-12064801, http://linkedlifedata.com/resource/pubmed/commentcorrection/18300266-12082021, http://linkedlifedata.com/resource/pubmed/commentcorrection/18300266-12490959, http://linkedlifedata.com/resource/pubmed/commentcorrection/18300266-1333439, http://linkedlifedata.com/resource/pubmed/commentcorrection/18300266-1355459, http://linkedlifedata.com/resource/pubmed/commentcorrection/18300266-1626600, http://linkedlifedata.com/resource/pubmed/commentcorrection/18300266-1688816, http://linkedlifedata.com/resource/pubmed/commentcorrection/18300266-2154753, http://linkedlifedata.com/resource/pubmed/commentcorrection/18300266-3295551, http://linkedlifedata.com/resource/pubmed/commentcorrection/18300266-6162992, http://linkedlifedata.com/resource/pubmed/commentcorrection/18300266-6629368, http://linkedlifedata.com/resource/pubmed/commentcorrection/18300266-7538480, http://linkedlifedata.com/resource/pubmed/commentcorrection/18300266-7767779, http://linkedlifedata.com/resource/pubmed/commentcorrection/18300266-7777494, http://linkedlifedata.com/resource/pubmed/commentcorrection/18300266-7853963, http://linkedlifedata.com/resource/pubmed/commentcorrection/18300266-7916405, http://linkedlifedata.com/resource/pubmed/commentcorrection/18300266-8137306, http://linkedlifedata.com/resource/pubmed/commentcorrection/18300266-8342999, http://linkedlifedata.com/resource/pubmed/commentcorrection/18300266-8644698, http://linkedlifedata.com/resource/pubmed/commentcorrection/18300266-9321410, http://linkedlifedata.com/resource/pubmed/commentcorrection/18300266-9481868, http://linkedlifedata.com/resource/pubmed/commentcorrection/18300266-9511847, http://linkedlifedata.com/resource/pubmed/commentcorrection/18300266-9517527, http://linkedlifedata.com/resource/pubmed/commentcorrection/18300266-9590426, http://linkedlifedata.com/resource/pubmed/commentcorrection/18300266-9635855
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Aug
pubmed:issn
1098-2744
pubmed:author
pubmed:copyrightInfo
(c) 2008 Wiley-Liss, Inc.
pubmed:issnType
Electronic
pubmed:volume
47
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
638-46
pubmed:dateRevised
2011-9-26
pubmed:meshHeading
pubmed:year
2008
pubmed:articleTitle
Increased susceptibility of chronic ulcerative colitis-induced carcinoma development in DNA repair enzyme Ogg1 deficient mice.
pubmed:affiliation
Department of Pathology, Northwestern University, Feinberg School of Medicine, Chicago, Illinois 60611, USA.
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't, Research Support, N.I.H., Extramural