Cited 6 times in
Synergistic Anticancer Activity of N-Hydroxy-7-(2-Naphthylthio) Heptanomide, Sorafenib, and Radiation Therapy in Patient-Derived Anaplastic Thyroid Cancer Models
DC Field | Value | Language |
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dc.contributor.author | 윤혁준 | - |
dc.contributor.author | 김희준 | - |
dc.contributor.author | 장항석 | - |
dc.contributor.author | 박정수 | - |
dc.contributor.author | 장호진 | - |
dc.contributor.author | 박기청 | - |
dc.date.accessioned | 2021-02-15T07:51:51Z | - |
dc.date.available | 2021-02-15T07:51:51Z | - |
dc.date.issued | 2021-01 | - |
dc.identifier.issn | 1661-6596 | - |
dc.identifier.uri | https://ir.ymlib.yonsei.ac.kr/handle/22282913/181661 | - |
dc.description.abstract | Anaplastic thyroid cancer (ATC) is an undifferentiated and advanced form of thyroid cancer, accompanied with a high ratio of epigenetic adjustment, which occurs more than genetic mutations. In this study, we aimed to evaluate the synergistic anticancer effect (in vitro and in vivo) of the new combination of N-hydroxy-7-(2-naphthylthio) heptanomide (HNHA) and sorafenib with radiation therapy in pre-clinical models of ATC. The ATC cell lines, YUMC-A1 and YUMC-A2, were isolated from the current patients who were treated with HNHA and sorafenib, either as monotherapy or combination therapy. Synergistic anticancer effect of the combination therapy on the intracellular signaling pathways and cell cycle was assessed via flow cytometry and immunoblot analysis. To examine tumor shrinkage activity in vivo, an ATC cell line-derived mouse xenograft model was used. Results showed that the combination therapy of HNHA and sorafenib with radiation promoted tumor suppression via caspase cleavage and cell cycle arrest in patient-derived ATC. In addition, the combination therapy of HNHA and sorafenib with radiation was more effective against ATC than therapy with HNHA or sorafenib with radiation. Thus, the combination of HNHA and sorafenib with radiation may be used as a novel curative approach for the treatment of ATC. | - |
dc.description.statementOfResponsibility | open | - |
dc.language | INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES | - |
dc.publisher | INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES | - |
dc.relation.isPartOf | INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES | - |
dc.rights | CC BY-NC-ND 2.0 KR | - |
dc.title | Synergistic Anticancer Activity of N-Hydroxy-7-(2-Naphthylthio) Heptanomide, Sorafenib, and Radiation Therapy in Patient-Derived Anaplastic Thyroid Cancer Models | - |
dc.type | Article | - |
dc.contributor.college | College of Medicine (의과대학) | - |
dc.contributor.department | Dept. of Surgery (외과학교실) | - |
dc.contributor.googleauthor | Hyeok Jun Yun | - |
dc.contributor.googleauthor | Hee Jun Kim | - |
dc.contributor.googleauthor | Jungmin Kim | - |
dc.contributor.googleauthor | Sang Yong Kim | - |
dc.contributor.googleauthor | Hang-Seok Chang | - |
dc.contributor.googleauthor | Cheong Soo Park | - |
dc.contributor.googleauthor | Ho-Jin Chang | - |
dc.contributor.googleauthor | Ki Cheong Park | - |
dc.identifier.doi | 10.3390/ijms22020536 | - |
dc.contributor.localId | A06022 | - |
dc.contributor.localId | A05236 | - |
dc.contributor.localId | A03488 | - |
dc.contributor.localId | A01645 | - |
dc.contributor.localId | A03496 | - |
dc.contributor.localId | A01449 | - |
dc.relation.journalcode | J01133 | - |
dc.identifier.eissn | 1422-0067 | - |
dc.identifier.pmid | 33430361 | - |
dc.subject.keyword | N-hydroxy-7-(2-naphthylthio) heptanomide | - |
dc.subject.keyword | apoptosis | - |
dc.subject.keyword | patient-derived anaplastic thyroid cancer | - |
dc.subject.keyword | radiation therapy | - |
dc.subject.keyword | sorafenib | - |
dc.contributor.alternativeName | Yun, Hyeok Jun | - |
dc.contributor.affiliatedAuthor | 윤혁준 | - |
dc.contributor.affiliatedAuthor | 김희준 | - |
dc.contributor.affiliatedAuthor | 장항석 | - |
dc.contributor.affiliatedAuthor | 박정수 | - |
dc.contributor.affiliatedAuthor | 장호진 | - |
dc.contributor.affiliatedAuthor | 박기청 | - |
dc.citation.volume | 22 | - |
dc.citation.number | 2 | - |
dc.citation.startPage | 536 | - |
dc.identifier.bibliographicCitation | INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, Vol.22(2) : 536, 2021-01 | - |
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