Citation Export
DC Field | Value | Language |
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dc.contributor.author | Kim, Kwang Hyeok | - |
dc.contributor.author | Kim, Jin Ock | - |
dc.contributor.author | Park, Jeong Yang | - |
dc.contributor.author | Seo, Min Duk | - |
dc.contributor.author | Park, Sang Gyu | - |
dc.date.issued | 2022-02-01 | - |
dc.identifier.uri | https://dspace.ajou.ac.kr/dev/handle/2018.oak/32549 | - |
dc.description.abstract | Lung cancer is the leading cause of cancer-related deaths. Small cell lung cancer (SCLC) accounts for 15–25% of all lung cancers. It exhibits a rapid doubling time and a high degree of invasiveness. Additionally, overexpression of c-Kit occurs in 70% of SCLC patients. In this study, we evaluated an antibody-drug conjugate (ADC) that targets c-Kit, which is a potential therapeutic agent for SCLC. First, we generated and characterized 4C9, a fully human antibody that targets c-Kit and specifically binds to SCLC cells expressing c-Kit with a binding affinity of KD = 5.5 × 10−9 M. Then, we developed an ADC using DM1, a microtubule inhibitor, as a payload. 4C9-DM1 efficiently induced apoptosis in SCLC with an IC50 ranging from 158 pM to 4 nM. An in vivo assay using a xenograft mouse model revealed a tumor growth inhibition (TGI) rate of 45% (3 mg/kg) and 59% (5 mg/kg) for 4C9-DM1 alone. Combination treatment with 4C9-DM1 plus carboplatin/etoposide or lurbinectedin resulted in a TGI rate greater than 90% compared with the vehicle control. Taken together, these results indicate that 4C9-DM1 is a potential therapeutic agent for SCLC treatment. | - |
dc.description.sponsorship | Funding: This research was supported by Novelty Nobility, grant number S-2022-c2040-00001. | - |
dc.language.iso | eng | - |
dc.publisher | MDPI | - |
dc.subject.mesh | Animals | - |
dc.subject.mesh | Antibodies, Monoclonal, Humanized | - |
dc.subject.mesh | Carboplatin | - |
dc.subject.mesh | Cell Line, Tumor | - |
dc.subject.mesh | Cell Proliferation | - |
dc.subject.mesh | Etoposide | - |
dc.subject.mesh | Female | - |
dc.subject.mesh | Humans | - |
dc.subject.mesh | Immunoconjugates | - |
dc.subject.mesh | Lung Neoplasms | - |
dc.subject.mesh | Maytansine | - |
dc.subject.mesh | Mice | - |
dc.subject.mesh | Proto-Oncogene Proteins c-kit | - |
dc.subject.mesh | Receptor Protein-Tyrosine Kinases | - |
dc.subject.mesh | Receptor, ErbB-2 | - |
dc.subject.mesh | Small Cell Lung Carcinoma | - |
dc.subject.mesh | Trastuzumab | - |
dc.subject.mesh | Tubulin Modulators | - |
dc.subject.mesh | Xenograft Model Antitumor Assays | - |
dc.title | Antibody-Drug Conjugate Targeting c-Kit for the Treatment of Small Cell Lung Cancer | - |
dc.type | Article | - |
dc.citation.title | International Journal of Molecular Sciences | - |
dc.citation.volume | 23 | - |
dc.identifier.bibliographicCitation | International Journal of Molecular Sciences, Vol.23 | - |
dc.identifier.doi | 10.3390/ijms23042264 | - |
dc.identifier.pmid | 35216379 | - |
dc.identifier.scopusid | 2-s2.0-85124874146 | - |
dc.identifier.url | https://www.mdpi.com/1422-0067/23/4/2264/pdf | - |
dc.subject.keyword | Antibody-drug conjugate | - |
dc.subject.keyword | C-Kit | - |
dc.subject.keyword | Monoclonal antibody | - |
dc.subject.keyword | Small cell lung cancer | - |
dc.description.isoa | true | - |
dc.subject.subarea | Catalysis | - |
dc.subject.subarea | Molecular Biology | - |
dc.subject.subarea | Spectroscopy | - |
dc.subject.subarea | Computer Science Applications | - |
dc.subject.subarea | Physical and Theoretical Chemistry | - |
dc.subject.subarea | Organic Chemistry | - |
dc.subject.subarea | Inorganic Chemistry | - |
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