Cited 5 times in
Discovery of New Anti-Cancer Agents against Patient-Derived Sorafenib-Resistant Papillary Thyroid Cancer
DC Field | Value | Language |
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dc.contributor.author | 김석모 | - |
dc.contributor.author | 김윤아 | - |
dc.contributor.author | 박기청 | - |
dc.contributor.author | 윤혁준 | - |
dc.date.accessioned | 2024-01-03T00:51:43Z | - |
dc.date.available | 2024-01-03T00:51:43Z | - |
dc.date.issued | 2023-11 | - |
dc.identifier.issn | 1661-6596 | - |
dc.identifier.uri | https://ir.ymlib.yonsei.ac.kr/handle/22282913/197392 | - |
dc.description.abstract | Thyroid cancer is the most well-known type of endocrine cancer that is easily treatable and can be completely cured in most cases. Nonetheless, anti-cancer drug-resistant metastasis or recurrence may occur and lead to the failure of cancer therapy, which eventually leads to the death of a patient with cancer. This study aimed to detect novel thyroid cancer target candidates based on validating and identifying one of many anti-cancer drug-resistant targets in patient-derived sorafenib-resistant papillary thyroid cancer (PTC). We focused on targeting the sarco/endoplasmic reticulum calcium ATPase (SERCA) in patient-derived sorafenib-resistant PTC cells compared with patient-derived sorafenib-sensitive PTC cells. We discovered novel SERCA inhibitors (candidates 33 and 36) by virtual screening. These candidates are novel SERCA inhibitors that lead to remarkable tumor shrinkage in a xenograft tumor model of sorafenib-resistant patient-derived PTC cells. These results are clinically valuable for the progression of novel combinatorial strategies that facultatively and efficiently target extremely malignant cancer cells, such as anti-cancer drug-resistant PTC cells. | - |
dc.description.statementOfResponsibility | open | - |
dc.language | English | - |
dc.publisher | MDPI | - |
dc.relation.isPartOf | INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES | - |
dc.rights | CC BY-NC-ND 2.0 KR | - |
dc.subject.MESH | Animals | - |
dc.subject.MESH | Antineoplastic Agents* / pharmacology | - |
dc.subject.MESH | Antineoplastic Agents* / therapeutic use | - |
dc.subject.MESH | Cell Line, Tumor | - |
dc.subject.MESH | Disease Models, Animal | - |
dc.subject.MESH | Humans | - |
dc.subject.MESH | Sorafenib / pharmacology | - |
dc.subject.MESH | Sorafenib / therapeutic use | - |
dc.subject.MESH | Thyroid Cancer, Papillary / drug therapy | - |
dc.subject.MESH | Thyroid Neoplasms* / drug therapy | - |
dc.subject.MESH | Thyroid Neoplasms* / pathology | - |
dc.title | Discovery of New Anti-Cancer Agents against Patient-Derived Sorafenib-Resistant Papillary Thyroid Cancer | - |
dc.type | Article | - |
dc.contributor.college | College of Medicine (의과대학) | - |
dc.contributor.department | Dept. of Surgery (외과학교실) | - |
dc.contributor.googleauthor | Yuna Kim | - |
dc.contributor.googleauthor | Hyeok Jun Yun | - |
dc.contributor.googleauthor | Kyung Hwa Choi | - |
dc.contributor.googleauthor | Chan Wung Kim | - |
dc.contributor.googleauthor | Jae Ha Lee | - |
dc.contributor.googleauthor | Raymond Weicker | - |
dc.contributor.googleauthor | Seok-Mo Kim | - |
dc.contributor.googleauthor | Ki Cheong Park | - |
dc.identifier.doi | 10.3390/ijms242216413 | - |
dc.contributor.localId | A00542 | - |
dc.contributor.localId | A06043 | - |
dc.contributor.localId | A01449 | - |
dc.contributor.localId | A06022 | - |
dc.relation.journalcode | J01133 | - |
dc.identifier.eissn | 1422-0067 | - |
dc.identifier.pmid | 38003602 | - |
dc.subject.keyword | anti-cancer drug resistant papillary thyroid cancer | - |
dc.subject.keyword | patient-derived papillary thyroid cancer | - |
dc.subject.keyword | sorafenib | - |
dc.contributor.alternativeName | Kim, Seok Mo | - |
dc.contributor.affiliatedAuthor | 김석모 | - |
dc.contributor.affiliatedAuthor | 김윤아 | - |
dc.contributor.affiliatedAuthor | 박기청 | - |
dc.contributor.affiliatedAuthor | 윤혁준 | - |
dc.citation.volume | 24 | - |
dc.citation.number | 22 | - |
dc.citation.startPage | 16413 | - |
dc.identifier.bibliographicCitation | INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, Vol.24(22) : 16413, 2023-11 | - |
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