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dc.contributor.authorSunwoo, Yun-Young
dc.contributor.authorLee, Jin-Hee
dc.contributor.authorJung, Ho Yong
dc.contributor.authorJung, Yu Jin
dc.contributor.authorPark, Moon-Seo
dc.contributor.authorChung, Yong-An
dc.contributor.authorMaeng, Lee-So
dc.contributor.authorHan, Young-Min
dc.contributor.authorShin, Hak Soo
dc.contributor.authorLee, Jisoo
dc.contributor.authorPark, Sang In
dc.date2022-08-11T08:09:43.000
dc.date.accessioned2022-08-23T16:40:49Z
dc.date.available2022-08-23T16:40:49Z
dc.date.issued2015-03-10
dc.date.submitted2015-09-02
dc.identifier.citationEvid Based Complement Alternat Med. 2015;2015:501508. doi: 10.1155/2015/501508. Epub 2015 Mar 10. <a href="http://dx.doi.org/10.1155/2015/501508">Link to article on publisher's site</a>
dc.identifier.issn1741-427X (Linking)
dc.identifier.doi10.1155/2015/501508
dc.identifier.pmid25852766
dc.identifier.urihttp://hdl.handle.net/20.500.14038/39758
dc.description.abstractOldenlandia diffusa (OD) is commonly used with various diseases such as cancer, arthritis, and autoimmune disease. Liver cirrhosis is a predominant risk factor for hepatocellular carcinoma (HCC). Here, we show that the therapeutic effect of OD, which was investigated both in vitro and chemically, induced HCC model. OD significantly enhanced apoptosis and antiproliferative activity and reduced migration ability of HCC cells. In vivo, OD was treated twice a day for 28 days after confirmed HCC model through 2-[(18)F]-fluoro-2-deoxy-D-glucose ((18)F-FDG) imaging. The survival in OD treated groups was shown to have a greater therapeutic effect than the control group. 28 days after OD treatment, OD treated groups resulted in a significant reduction in tumor number, size, (18)F-FDG uptake, and serum levels such as alanine transaminase, aspartate transaminase, and alkaline phosphate compared to the control group. Also, proliferated cells in tumor sites by OD were reduced compared to the control group. Furthermore, several rats in OD treated group survived over 60 days and liver morphology of these rats showed the difference between tumor mass and normal tissue. These results suggest that OD may have antiproliferative activity, inhibition of metastasis, and apoptotic effects in chemically induced HCC model and can have the potential use for clinical application as anticancer drug of the herbal extract.
dc.language.isoen_US
dc.relation<a href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=pubmed&cmd=Retrieve&list_uids=25852766&dopt=Abstract">Link to Article in PubMed</a>
dc.rights<p>Copyright © 2015 Yun-Young Sunwoo et al. This is an open access article distributed under the <a href="http://creativecommons.org/licenses/by/3.0/">Creative Commons Attribution License</a>, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.</p>
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/
dc.subjectAlternative and Complementary Medicine
dc.subjectDigestive System Diseases
dc.subjectNeoplasms
dc.subjectOncology
dc.titleOldenlandia diffusa Promotes Antiproliferative and Apoptotic Effects in a Rat Hepatocellular Carcinoma with Liver Cirrhosis
dc.typeJournal Article
dc.source.journaltitleEvidence-based complementary and alternative medicine : eCAM
dc.source.volume2015
dc.identifier.legacyfulltexthttps://escholarship.umassmed.edu/cgi/viewcontent.cgi?article=3560&amp;context=oapubs&amp;unstamped=1
dc.identifier.legacycoverpagehttps://escholarship.umassmed.edu/oapubs/2556
dc.identifier.contextkey7548588
refterms.dateFOA2022-08-23T16:40:49Z
html.description.abstract<p>Oldenlandia diffusa (OD) is commonly used with various diseases such as cancer, arthritis, and autoimmune disease. Liver cirrhosis is a predominant risk factor for hepatocellular carcinoma (HCC). Here, we show that the therapeutic effect of OD, which was investigated both in vitro and chemically, induced HCC model. OD significantly enhanced apoptosis and antiproliferative activity and reduced migration ability of HCC cells. In vivo, OD was treated twice a day for 28 days after confirmed HCC model through 2-[(18)F]-fluoro-2-deoxy-D-glucose ((18)F-FDG) imaging. The survival in OD treated groups was shown to have a greater therapeutic effect than the control group. 28 days after OD treatment, OD treated groups resulted in a significant reduction in tumor number, size, (18)F-FDG uptake, and serum levels such as alanine transaminase, aspartate transaminase, and alkaline phosphate compared to the control group. Also, proliferated cells in tumor sites by OD were reduced compared to the control group. Furthermore, several rats in OD treated group survived over 60 days and liver morphology of these rats showed the difference between tumor mass and normal tissue. These results suggest that OD may have antiproliferative activity, inhibition of metastasis, and apoptotic effects in chemically induced HCC model and can have the potential use for clinical application as anticancer drug of the herbal extract.</p>
dc.identifier.submissionpathoapubs/2556
dc.contributor.departmentDepartment of Internal Medicine
dc.source.pages501508


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<p>Copyright © 2015 Yun-Young Sunwoo et al. This is an open access article distributed under the <a href="http://creativecommons.org/licenses/by/3.0/">Creative Commons Attribution License</a>, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.</p>
Except where otherwise noted, this item's license is described as <p>Copyright © 2015 Yun-Young Sunwoo et al. This is an open access article distributed under the <a href="http://creativecommons.org/licenses/by/3.0/">Creative Commons Attribution License</a>, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.</p>