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Study the inhibitory effect and mechanism of the ethanol extract of deziyangxin on LLC cells

BACKGROUND: Chinese Tibetan medicine plays a crucial role in complementary anti-tumor treatments. This article aims to investigate the inhibitory effect of the alcoholic extract of Tibetan medicine Deziyangxin (DZYX) on the proliferation and migration of non-small cell lung cancer (NSCLC) cells, spe...

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Autores principales: Yun, Yi, Yahui, Jiang, Bobo, Bai, Caifeng, Zhang, Yanli, Zhao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10432991/
https://www.ncbi.nlm.nih.gov/pubmed/37600386
http://dx.doi.org/10.1016/j.heliyon.2023.e18712
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author Yun, Yi
Yahui, Jiang
Bobo, Bai
Caifeng, Zhang
Yanli, Zhao
author_facet Yun, Yi
Yahui, Jiang
Bobo, Bai
Caifeng, Zhang
Yanli, Zhao
author_sort Yun, Yi
collection PubMed
description BACKGROUND: Chinese Tibetan medicine plays a crucial role in complementary anti-tumor treatments. This article aims to investigate the inhibitory effect of the alcoholic extract of Tibetan medicine Deziyangxin (DZYX) on the proliferation and migration of non-small cell lung cancer (NSCLC) cells, specifically LLC cells, as well as explore its potential mechanism of action. METHODS: The effect of the alcoholic extract on LLC cell viability was assessed using the CCK-8 method. The proliferation of LLC cells was evaluated using the EdU (5-Acetyl-2'-deoxyuridine) assay. Transwell assays were conducted to measure cell metastasis. Western blot analysis was performed to assess the expression of Cleaved Caspase-3, Bcl-2, Beciln-1, indicating the impact of DZYX on apoptosis and autophagy in LLC cells. Furthermore, the anti-tumor mechanism of DZYX was explored through transcriptome research and detection of Akt, p-Akt, p-mTOR protein levels. RESULTS: The ethanol extract of DZYX exhibited a concentration-dependent and time-dependent inhibitory effect on LLC cell viability, with an IC50 of 406.1 μg/ml. Moreover, the ethanol extract of DZYX significantly reduced the migration ability of LLC cells. Additionally, the alcoholic extract of DZYX upregulated the expression of Cleaved Caspase-3 and Beciln-1 proteins, while downregulating the expression of Bcl-2 in LLC cells. Importantly, DZYX ethanol extract down regulated the expression of Akt and p-mTOR proteins in LLC cells, which combined with transcriptome results indicated that the drug exerted a multi-target and multi-pathway effect, primarily related to inhibiting the activation of the PI3K/AKT/m-TOR signaling pathway. CONCLUSION: The alcoholic extract of DZYX demonstrates inhibitory effects on LLC cells, promoting apoptosis and autophagy. It is hypothesized that its anti-tumor mechanism is associated with the PI3K/AKT/m-TOR pathway.
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spelling pubmed-104329912023-08-18 Study the inhibitory effect and mechanism of the ethanol extract of deziyangxin on LLC cells Yun, Yi Yahui, Jiang Bobo, Bai Caifeng, Zhang Yanli, Zhao Heliyon Research Article BACKGROUND: Chinese Tibetan medicine plays a crucial role in complementary anti-tumor treatments. This article aims to investigate the inhibitory effect of the alcoholic extract of Tibetan medicine Deziyangxin (DZYX) on the proliferation and migration of non-small cell lung cancer (NSCLC) cells, specifically LLC cells, as well as explore its potential mechanism of action. METHODS: The effect of the alcoholic extract on LLC cell viability was assessed using the CCK-8 method. The proliferation of LLC cells was evaluated using the EdU (5-Acetyl-2'-deoxyuridine) assay. Transwell assays were conducted to measure cell metastasis. Western blot analysis was performed to assess the expression of Cleaved Caspase-3, Bcl-2, Beciln-1, indicating the impact of DZYX on apoptosis and autophagy in LLC cells. Furthermore, the anti-tumor mechanism of DZYX was explored through transcriptome research and detection of Akt, p-Akt, p-mTOR protein levels. RESULTS: The ethanol extract of DZYX exhibited a concentration-dependent and time-dependent inhibitory effect on LLC cell viability, with an IC50 of 406.1 μg/ml. Moreover, the ethanol extract of DZYX significantly reduced the migration ability of LLC cells. Additionally, the alcoholic extract of DZYX upregulated the expression of Cleaved Caspase-3 and Beciln-1 proteins, while downregulating the expression of Bcl-2 in LLC cells. Importantly, DZYX ethanol extract down regulated the expression of Akt and p-mTOR proteins in LLC cells, which combined with transcriptome results indicated that the drug exerted a multi-target and multi-pathway effect, primarily related to inhibiting the activation of the PI3K/AKT/m-TOR signaling pathway. CONCLUSION: The alcoholic extract of DZYX demonstrates inhibitory effects on LLC cells, promoting apoptosis and autophagy. It is hypothesized that its anti-tumor mechanism is associated with the PI3K/AKT/m-TOR pathway. Elsevier 2023-07-27 /pmc/articles/PMC10432991/ /pubmed/37600386 http://dx.doi.org/10.1016/j.heliyon.2023.e18712 Text en © 2023 Published by Elsevier Ltd. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Research Article
Yun, Yi
Yahui, Jiang
Bobo, Bai
Caifeng, Zhang
Yanli, Zhao
Study the inhibitory effect and mechanism of the ethanol extract of deziyangxin on LLC cells
title Study the inhibitory effect and mechanism of the ethanol extract of deziyangxin on LLC cells
title_full Study the inhibitory effect and mechanism of the ethanol extract of deziyangxin on LLC cells
title_fullStr Study the inhibitory effect and mechanism of the ethanol extract of deziyangxin on LLC cells
title_full_unstemmed Study the inhibitory effect and mechanism of the ethanol extract of deziyangxin on LLC cells
title_short Study the inhibitory effect and mechanism of the ethanol extract of deziyangxin on LLC cells
title_sort study the inhibitory effect and mechanism of the ethanol extract of deziyangxin on llc cells
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10432991/
https://www.ncbi.nlm.nih.gov/pubmed/37600386
http://dx.doi.org/10.1016/j.heliyon.2023.e18712
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