Suppression of HIF-1α accumulation by betulinic acid through proteasome activation in hypoxic cervical cancer

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dc.contributor.authorHwee Jin Kim-
dc.contributor.authorHyun Soo Cho-
dc.contributor.authorHyun Seung Ban-
dc.contributor.authorH Nakamura-
dc.date.accessioned2020-04-24T16:30:14Z-
dc.date.available2020-04-24T16:30:14Z-
dc.date.issued2020-
dc.identifier.issn0006-291X-
dc.identifier.uri10.1016/j.bbrc.2020.01.031ko
dc.identifier.urihttps://oak.kribb.re.kr/handle/201005/19355-
dc.description.abstractBetulinic acid (BA) exhibits various biological activities such as anti-bacterial, anti-inflammatory, anti-human papilloma virus (HPV), and anti-cancer activities. HPV infection is associated with a high risk of cervical cancer, which is the leading cause of deaths among women worldwide. Therefore, BA is an attractive therapeutic agent for treating cervical cancer. In this study, we investigated the role of BA in regulating the hypoxia-mediated response in HeLa cells and clarified the underlying mechanism of action. We found that BA inhibited the hypoxia-induced accumulation of HIF-1α without affecting HIF-1α mRNA levels and suppressed the expression of HIF target genes, including VEGF, GLUT1, and PDK1 in HeLa cells. Additionally, BA enhanced the β1, β2, and β5 activities of the proteasome, which resulted in reduced levels of ubiquitinated proteins and HIF-1α protein in HeLa cells. However, BA treatment did not affect the deubiquitinase enzyme activity in HeLa cells. These results indicate that inhibition of HIF-1α accumulation by BA is mediated by activation of the proteasome, and BA is a potential anticancer agent for the regulation of the HIF signaling pathway.-
dc.publisherElsevier-
dc.titleSuppression of HIF-1α accumulation by betulinic acid through proteasome activation in hypoxic cervical cancer-
dc.title.alternativeSuppression of HIF-1α accumulation by betulinic acid through proteasome activation in hypoxic cervical cancer-
dc.typeArticle-
dc.citation.titleBiochemical and Biophysical Research Communications-
dc.citation.number3-
dc.citation.endPage732-
dc.citation.startPage726-
dc.citation.volume523-
dc.contributor.affiliatedAuthorHwee Jin Kim-
dc.contributor.affiliatedAuthorHyun Soo Cho-
dc.contributor.affiliatedAuthorHyun Seung Ban-
dc.contributor.alternativeName김휘진-
dc.contributor.alternativeName조현수-
dc.contributor.alternativeName반현승-
dc.contributor.alternativeNameNakamura-
dc.identifier.bibliographicCitationBiochemical and Biophysical Research Communications, vol. 523, no. 3, pp. 726-732-
dc.identifier.doi10.1016/j.bbrc.2020.01.031-
dc.subject.keywordBetulinic acid-
dc.subject.keywordCancer-
dc.subject.keywordHypoxia-
dc.subject.keywordHypoxia-inducible factor-
dc.subject.keywordProteasome-
dc.subject.keywordUbiquitination-
dc.subject.localBetulinic acid-
dc.subject.localbetulinic acid-
dc.subject.localCancers-
dc.subject.localcancer-
dc.subject.localCancer-
dc.subject.localhypoxia-
dc.subject.localHypoxia-
dc.subject.localhypoxia-inducible factor (HIF)-
dc.subject.localHypoxia-inducible factor-
dc.subject.localhypoxia-inducible factor-
dc.subject.localHYPOXIA INDUCIBLE FACTOR-
dc.subject.localHypoxia-inducible factor (HIF)-
dc.subject.localproteasome-
dc.subject.localProteasome-
dc.subject.localUbiquitination-
dc.subject.localubiquitination-
dc.description.journalClassY-
Appears in Collections:
Division of Research on National Challenges > Stem Cell Convergenece Research Center > 1. Journal Articles
Division of A.I. & Biomedical Research > Biotherapeutics Translational Research Center > 1. Journal Articles
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