GAD 67KD antisense in colon cancer cells inhibits cell growth and sensitizes to butyrate and pH reduction and H2O2 and γ-radiation

Cited 17 time in scopus
Metadata Downloads

Full metadata record

DC FieldValueLanguage
dc.contributor.authorM S Moon-
dc.contributor.authorEun Wie Cho-
dc.contributor.authorH S Byun-
dc.contributor.authorI L Jung-
dc.contributor.authorI G Kim-
dc.date.accessioned2017-04-19T09:02:00Z-
dc.date.available2017-04-19T09:02:00Z-
dc.date.issued2004-
dc.identifier.issn0096-9621-
dc.identifier.uri10.1016/j.abb.2004.07.015ko
dc.identifier.urihttps://oak.kribb.re.kr/handle/201005/6751-
dc.description.abstractIn eukaryotes, glutamate decarboxylase (GAD) expression was found in brain, kidney, and several kinds of tumor tissues. But its function has been emphasized only as a neurotransmitter-synthesizer, the role in controlling intracellular physiology is poorly understood. According to our studies, when GAD 67KD expression in colon cancer HT-29 cell was repressed by antisense DNA, the cell proliferation was significantly inhibited. GAD 67KD antisensed cells exhibited the low glutathione and high reactive oxygen species level. More importantly, these cells were extremely sensitive to butyrate or pH reduction, both of which naturally cause metabolic stress in the colon lumen, as well as H2O2 and ionizing radiation. These data indicate that GAD 67KD regulates the intracellular redox potential and is important for resistance to acidic or oxidative stress. So, based on these results, we suggest that inhibition of GAD 67KD expression has potentially important implications for overcoming the drug resistance of cancer cells.-
dc.publisherElsevier-
dc.titleGAD 67KD antisense in colon cancer cells inhibits cell growth and sensitizes to butyrate and pH reduction and H2O2 and γ-radiation-
dc.title.alternativeGAD 67KD antisense in colon cancer cells inhibits cell growth and sensitizes to butyrate and pH reduction and H2O2 and γ-radiation-
dc.typeArticle-
dc.citation.titleArchives of Biochemistry and Biophysics-
dc.citation.number2-
dc.citation.endPage236-
dc.citation.startPage229-
dc.citation.volume430-
dc.contributor.affiliatedAuthorEun Wie Cho-
dc.contributor.alternativeName문명숙-
dc.contributor.alternativeName조은위-
dc.contributor.alternativeName변희순-
dc.contributor.alternativeName정일래-
dc.contributor.alternativeName김인규-
dc.identifier.bibliographicCitationArchives of Biochemistry and Biophysics, vol. 430, no. 2, pp. 229-236-
dc.identifier.doi10.1016/j.abb.2004.07.015-
dc.subject.keywordDrug resistance-
dc.subject.keywordGlutamate decarboxylase-
dc.subject.keywordGlutathione-
dc.subject.keywordIonizing radiation-
dc.subject.keywordReactive oxygen species-
dc.subject.localDrug resistance-
dc.subject.localDrug-resistance-
dc.subject.localdrug-resistance-
dc.subject.localdrug resistance-
dc.subject.localGlutamate decarboxylase-
dc.subject.localGlutathione-
dc.subject.localglutathione-
dc.subject.localIonizing radiation-
dc.subject.localIonizing radiation (IR)-
dc.subject.localionizing radiation-
dc.subject.localROS-
dc.subject.localReactive Oxygen Species (ROS)-
dc.subject.localReactive oxidative species-
dc.subject.localReactive oxygen species-
dc.subject.localReactive oxygen species (ROS)-
dc.subject.localreactive oxygen species-
dc.subject.localreactive oxygen species (ROS)-
dc.subject.localReactive Oxygen Species-
dc.subject.localReactive oxygen species(ROS)-
dc.description.journalClassY-
Appears in Collections:
Division of A.I. & Biomedical Research > Orphan Disease Therapeutic Target Research Center > 1. Journal Articles
Files in This Item:
  • There are no files associated with this item.


Items in OpenAccess@KRIBB are protected by copyright, with all rights reserved, unless otherwise indicated.