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Antibody-Drug Conjugate Targeting c-Kit for the Treatment of Small Cell Lung Canceroa mark
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Publication Year
2022-02-01
Publisher
MDPI
Citation
International Journal of Molecular Sciences, Vol.23
Keyword
Antibody-drug conjugateC-KitMonoclonal antibodySmall cell lung cancer
Mesh Keyword
AnimalsAntibodies, Monoclonal, HumanizedCarboplatinCell Line, TumorCell ProliferationEtoposideFemaleHumansImmunoconjugatesLung NeoplasmsMaytansineMiceProto-Oncogene Proteins c-kitReceptor Protein-Tyrosine KinasesReceptor, ErbB-2Small Cell Lung CarcinomaTrastuzumabTubulin ModulatorsXenograft Model Antitumor Assays
All Science Classification Codes (ASJC)
CatalysisMolecular BiologySpectroscopyComputer Science ApplicationsPhysical and Theoretical ChemistryOrganic ChemistryInorganic Chemistry
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.
Language
eng
URI
https://dspace.ajou.ac.kr/dev/handle/2018.oak/32549
DOI
https://doi.org/10.3390/ijms23042264
Fulltext

Type
Article
Funding
Funding: This research was supported by Novelty Nobility, grant number S-2022-c2040-00001.
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Seo, Min-Duk서민덕
Division of Pharmacy Sciences
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