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Synergistic Antitumor Activity of SH003 and Docetaxel via EGFR Signaling Inhibition in Non-Small Cell Lung Cancer
Epidermal growth factor receptor (EGFR) is overexpressed in lung cancer patients. Despite treatment with various EGFR tyrosine kinase inhibitors, recurrence and metastasis of lung cancer are inevitable. Docetaxel (DTX) is an effective conventional drug that is used to treat various cancers. Several...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8395077/ https://www.ncbi.nlm.nih.gov/pubmed/34445110 http://dx.doi.org/10.3390/ijms22168405 |
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author | Jeong, Mi-So Lee, Kang-Wook Choi, Yu-Jeong Kim, Yun-Gyeong Hwang, Hyun-Ha Lee, Seo-Yeon Jung, Se-Eun Park, Sun-Ah Lee, Jin-Hee Joo, Yong-Joon Cho, Sung-Gook Ko, Seong-Gyu |
author_facet | Jeong, Mi-So Lee, Kang-Wook Choi, Yu-Jeong Kim, Yun-Gyeong Hwang, Hyun-Ha Lee, Seo-Yeon Jung, Se-Eun Park, Sun-Ah Lee, Jin-Hee Joo, Yong-Joon Cho, Sung-Gook Ko, Seong-Gyu |
author_sort | Jeong, Mi-So |
collection | PubMed |
description | Epidermal growth factor receptor (EGFR) is overexpressed in lung cancer patients. Despite treatment with various EGFR tyrosine kinase inhibitors, recurrence and metastasis of lung cancer are inevitable. Docetaxel (DTX) is an effective conventional drug that is used to treat various cancers. Several researchers have studied the use of traditional herbal medicine in combination with docetaxel, to improve lung cancer treatment. SH003, a novel herbal mixture, exerts anticancer effects in different cancer cell types. Here, we aimed to investigate the apoptotic and anticancer effects of SH003 in combination with DTX, in human non-small-cell lung cancer (NSCLC). SH003, with DTX, induced apoptotic cell death, with increased expression of cleaved caspases and cleaved poly (ADP-ribose) polymerase in NSCLC cells. Moreover, SH003 and DTX induced the apoptosis of H460 cells via the suppression of the EGFR and signal transducer and activator of transcription 3 (STAT3) signaling pathways. In H460 tumor xenograft models, the administration of SH003 or docetaxel alone diminished tumor growth, and their combination effectively killed cancer cells, with increased expression of apoptotic markers and decreased expression of p-EGFR and p-STAT3. Collectively, the combination of SH003 and DTX may be a novel anticancer strategy to overcome the challenges that are associated with conventional lung cancer therapy. |
format | Online Article Text |
id | pubmed-8395077 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-83950772021-08-28 Synergistic Antitumor Activity of SH003 and Docetaxel via EGFR Signaling Inhibition in Non-Small Cell Lung Cancer Jeong, Mi-So Lee, Kang-Wook Choi, Yu-Jeong Kim, Yun-Gyeong Hwang, Hyun-Ha Lee, Seo-Yeon Jung, Se-Eun Park, Sun-Ah Lee, Jin-Hee Joo, Yong-Joon Cho, Sung-Gook Ko, Seong-Gyu Int J Mol Sci Article Epidermal growth factor receptor (EGFR) is overexpressed in lung cancer patients. Despite treatment with various EGFR tyrosine kinase inhibitors, recurrence and metastasis of lung cancer are inevitable. Docetaxel (DTX) is an effective conventional drug that is used to treat various cancers. Several researchers have studied the use of traditional herbal medicine in combination with docetaxel, to improve lung cancer treatment. SH003, a novel herbal mixture, exerts anticancer effects in different cancer cell types. Here, we aimed to investigate the apoptotic and anticancer effects of SH003 in combination with DTX, in human non-small-cell lung cancer (NSCLC). SH003, with DTX, induced apoptotic cell death, with increased expression of cleaved caspases and cleaved poly (ADP-ribose) polymerase in NSCLC cells. Moreover, SH003 and DTX induced the apoptosis of H460 cells via the suppression of the EGFR and signal transducer and activator of transcription 3 (STAT3) signaling pathways. In H460 tumor xenograft models, the administration of SH003 or docetaxel alone diminished tumor growth, and their combination effectively killed cancer cells, with increased expression of apoptotic markers and decreased expression of p-EGFR and p-STAT3. Collectively, the combination of SH003 and DTX may be a novel anticancer strategy to overcome the challenges that are associated with conventional lung cancer therapy. MDPI 2021-08-05 /pmc/articles/PMC8395077/ /pubmed/34445110 http://dx.doi.org/10.3390/ijms22168405 Text en © 2021 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 Jeong, Mi-So Lee, Kang-Wook Choi, Yu-Jeong Kim, Yun-Gyeong Hwang, Hyun-Ha Lee, Seo-Yeon Jung, Se-Eun Park, Sun-Ah Lee, Jin-Hee Joo, Yong-Joon Cho, Sung-Gook Ko, Seong-Gyu Synergistic Antitumor Activity of SH003 and Docetaxel via EGFR Signaling Inhibition in Non-Small Cell Lung Cancer |
title | Synergistic Antitumor Activity of SH003 and Docetaxel via EGFR Signaling Inhibition in Non-Small Cell Lung Cancer |
title_full | Synergistic Antitumor Activity of SH003 and Docetaxel via EGFR Signaling Inhibition in Non-Small Cell Lung Cancer |
title_fullStr | Synergistic Antitumor Activity of SH003 and Docetaxel via EGFR Signaling Inhibition in Non-Small Cell Lung Cancer |
title_full_unstemmed | Synergistic Antitumor Activity of SH003 and Docetaxel via EGFR Signaling Inhibition in Non-Small Cell Lung Cancer |
title_short | Synergistic Antitumor Activity of SH003 and Docetaxel via EGFR Signaling Inhibition in Non-Small Cell Lung Cancer |
title_sort | synergistic antitumor activity of sh003 and docetaxel via egfr signaling inhibition in non-small cell lung cancer |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8395077/ https://www.ncbi.nlm.nih.gov/pubmed/34445110 http://dx.doi.org/10.3390/ijms22168405 |
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