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A CD276-Targeted Antibody-Drug Conjugate to Treat Non-Small Lung Cancer (NSCLC)
Non-small cell lung cancer (NSCLC) patients, accounting for approximately 85% of lung cancer cases, are usually diagnosed in advanced stages. Traditional surgical resection and radiotherapy have very limited clinical benefits. The objective of this study was to develop and evaluate a targeted therap...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10572050/ https://www.ncbi.nlm.nih.gov/pubmed/37830607 http://dx.doi.org/10.3390/cells12192393 |
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author | Zhang, Jiashuai Zhou, Zhuoxin (Zora) Chen, Kai Kim, Seulhee Cho, Irene Soohyun Varadkar, Tanvi Baker, Hailey Cho, Ju Hwan Zhou, Lufang Liu, Xiaoguang (Margaret) |
author_facet | Zhang, Jiashuai Zhou, Zhuoxin (Zora) Chen, Kai Kim, Seulhee Cho, Irene Soohyun Varadkar, Tanvi Baker, Hailey Cho, Ju Hwan Zhou, Lufang Liu, Xiaoguang (Margaret) |
author_sort | Zhang, Jiashuai |
collection | PubMed |
description | Non-small cell lung cancer (NSCLC) patients, accounting for approximately 85% of lung cancer cases, are usually diagnosed in advanced stages. Traditional surgical resection and radiotherapy have very limited clinical benefits. The objective of this study was to develop and evaluate a targeted therapy, antibody-drug conjugate (ADC), for NSCLC treatment. Specifically, the CD276 receptor was evaluated and confirmed as an ideal surface target of NSCLC in the immunohistochemistry (IHC) staining of seventy-three patient tumor microarrays and western blotting analysis of eight cell lines. Our anti-CD276 monoclonal antibody (mAb) with cross-activity to both human and mouse receptors showed high surface binding, effective drug delivery and tumor-specific targeting in flow cytometry, confocal microscopy, and in vivo imaging system analysis. The ADC constructed with our CD276 mAb and payload monomethyl auristatin F (MMAF) showed high anti-NSCLC cytotoxicity to multiple lines and effective anti-tumor efficacy in both immunocompromised and immunocompetent NSCLC xenograft mouse models. The brief mechanism study revealed the integration of cell proliferation inhibition and immune cell reactivation in tumor microenvironments. The toxicity study did not detect off-target immune toxicity or peripheral toxicity. Altogether, this study suggested that anti-CD276 ADC could be a promising candidate for NSCLC treatment. |
format | Online Article Text |
id | pubmed-10572050 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-105720502023-10-14 A CD276-Targeted Antibody-Drug Conjugate to Treat Non-Small Lung Cancer (NSCLC) Zhang, Jiashuai Zhou, Zhuoxin (Zora) Chen, Kai Kim, Seulhee Cho, Irene Soohyun Varadkar, Tanvi Baker, Hailey Cho, Ju Hwan Zhou, Lufang Liu, Xiaoguang (Margaret) Cells Article Non-small cell lung cancer (NSCLC) patients, accounting for approximately 85% of lung cancer cases, are usually diagnosed in advanced stages. Traditional surgical resection and radiotherapy have very limited clinical benefits. The objective of this study was to develop and evaluate a targeted therapy, antibody-drug conjugate (ADC), for NSCLC treatment. Specifically, the CD276 receptor was evaluated and confirmed as an ideal surface target of NSCLC in the immunohistochemistry (IHC) staining of seventy-three patient tumor microarrays and western blotting analysis of eight cell lines. Our anti-CD276 monoclonal antibody (mAb) with cross-activity to both human and mouse receptors showed high surface binding, effective drug delivery and tumor-specific targeting in flow cytometry, confocal microscopy, and in vivo imaging system analysis. The ADC constructed with our CD276 mAb and payload monomethyl auristatin F (MMAF) showed high anti-NSCLC cytotoxicity to multiple lines and effective anti-tumor efficacy in both immunocompromised and immunocompetent NSCLC xenograft mouse models. The brief mechanism study revealed the integration of cell proliferation inhibition and immune cell reactivation in tumor microenvironments. The toxicity study did not detect off-target immune toxicity or peripheral toxicity. Altogether, this study suggested that anti-CD276 ADC could be a promising candidate for NSCLC treatment. MDPI 2023-09-30 /pmc/articles/PMC10572050/ /pubmed/37830607 http://dx.doi.org/10.3390/cells12192393 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Zhang, Jiashuai Zhou, Zhuoxin (Zora) Chen, Kai Kim, Seulhee Cho, Irene Soohyun Varadkar, Tanvi Baker, Hailey Cho, Ju Hwan Zhou, Lufang Liu, Xiaoguang (Margaret) A CD276-Targeted Antibody-Drug Conjugate to Treat Non-Small Lung Cancer (NSCLC) |
title | A CD276-Targeted Antibody-Drug Conjugate to Treat Non-Small Lung Cancer (NSCLC) |
title_full | A CD276-Targeted Antibody-Drug Conjugate to Treat Non-Small Lung Cancer (NSCLC) |
title_fullStr | A CD276-Targeted Antibody-Drug Conjugate to Treat Non-Small Lung Cancer (NSCLC) |
title_full_unstemmed | A CD276-Targeted Antibody-Drug Conjugate to Treat Non-Small Lung Cancer (NSCLC) |
title_short | A CD276-Targeted Antibody-Drug Conjugate to Treat Non-Small Lung Cancer (NSCLC) |
title_sort | cd276-targeted antibody-drug conjugate to treat non-small lung cancer (nsclc) |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10572050/ https://www.ncbi.nlm.nih.gov/pubmed/37830607 http://dx.doi.org/10.3390/cells12192393 |
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