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Polyphenol Oxidase as a Promising Alternative Therapeutic Agent for Cancer Therapy
Cancers have always been the most difficult to fight, the treatment of cancer is still not considered. Thus, exploring new anticancer drugs is still imminent. Traditional Chinese medicine has played an important role in the treatment of cancer. Polyphenol oxidase (PPO) extracted from Edible mushroom...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8911857/ https://www.ncbi.nlm.nih.gov/pubmed/35268616 http://dx.doi.org/10.3390/molecules27051515 |
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author | Yuan, Qinqin Guo, Huixia Ding, Jiajie Jiao, Chan Qi, Yalei Zafar, Hajra Ma, Xueyun Raza, Faisal Han, Jianqiu |
author_facet | Yuan, Qinqin Guo, Huixia Ding, Jiajie Jiao, Chan Qi, Yalei Zafar, Hajra Ma, Xueyun Raza, Faisal Han, Jianqiu |
author_sort | Yuan, Qinqin |
collection | PubMed |
description | Cancers have always been the most difficult to fight, the treatment of cancer is still not considered. Thus, exploring new anticancer drugs is still imminent. Traditional Chinese medicine has played an important role in the treatment of cancer. Polyphenol oxidase (PPO) extracted from Edible mushroom has many related reports on its characteristics, but its role in cancer treatment is still unclear. This study aims to investigate the effects of PPO extracted from Edible mushroom on the proliferation, migration, invasion, and apoptosis of cancer cells in vitro and explore the therapeutic effects of PPO on tumors in vivo. A cell counting kit-8 (CCK8) assay was used to detect the effect of PPO on the proliferation of cancer cells. The effect of PPO on cancer cell migration ability was detected by scratch test. The effect of PPO on the invasion ability of cancer cells was detected by a transwell assay. The effect of PPO on the apoptosis of cancer cells was detected by flow cytometry. Female BALB/c mice (18–25 g, 6–8 weeks) were used for in vivo experiments. The experiments were divided into control group, model group, low-dose group (25 mg/kg), and high-dose group (50 mg/kg). In vitro, PPO extracted from Edible mushroom significantly inhibited the proliferation, migration, and invasion capability of breast cancer cell 4T1, lung cancer cell A549, and prostate cancer cell C4-2, and significantly promoted the apoptosis of 4T1, A549, and C4-2. In vivo experiments showed PPO inhibitory effect on tumor growth. Collectively, the edible fungus extract PPO could play an effective role in treating various cancers, and it may potentially be a promising agent for treating cancers. |
format | Online Article Text |
id | pubmed-8911857 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-89118572022-03-11 Polyphenol Oxidase as a Promising Alternative Therapeutic Agent for Cancer Therapy Yuan, Qinqin Guo, Huixia Ding, Jiajie Jiao, Chan Qi, Yalei Zafar, Hajra Ma, Xueyun Raza, Faisal Han, Jianqiu Molecules Article Cancers have always been the most difficult to fight, the treatment of cancer is still not considered. Thus, exploring new anticancer drugs is still imminent. Traditional Chinese medicine has played an important role in the treatment of cancer. Polyphenol oxidase (PPO) extracted from Edible mushroom has many related reports on its characteristics, but its role in cancer treatment is still unclear. This study aims to investigate the effects of PPO extracted from Edible mushroom on the proliferation, migration, invasion, and apoptosis of cancer cells in vitro and explore the therapeutic effects of PPO on tumors in vivo. A cell counting kit-8 (CCK8) assay was used to detect the effect of PPO on the proliferation of cancer cells. The effect of PPO on cancer cell migration ability was detected by scratch test. The effect of PPO on the invasion ability of cancer cells was detected by a transwell assay. The effect of PPO on the apoptosis of cancer cells was detected by flow cytometry. Female BALB/c mice (18–25 g, 6–8 weeks) were used for in vivo experiments. The experiments were divided into control group, model group, low-dose group (25 mg/kg), and high-dose group (50 mg/kg). In vitro, PPO extracted from Edible mushroom significantly inhibited the proliferation, migration, and invasion capability of breast cancer cell 4T1, lung cancer cell A549, and prostate cancer cell C4-2, and significantly promoted the apoptosis of 4T1, A549, and C4-2. In vivo experiments showed PPO inhibitory effect on tumor growth. Collectively, the edible fungus extract PPO could play an effective role in treating various cancers, and it may potentially be a promising agent for treating cancers. MDPI 2022-02-23 /pmc/articles/PMC8911857/ /pubmed/35268616 http://dx.doi.org/10.3390/molecules27051515 Text en © 2022 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 Yuan, Qinqin Guo, Huixia Ding, Jiajie Jiao, Chan Qi, Yalei Zafar, Hajra Ma, Xueyun Raza, Faisal Han, Jianqiu Polyphenol Oxidase as a Promising Alternative Therapeutic Agent for Cancer Therapy |
title | Polyphenol Oxidase as a Promising Alternative Therapeutic Agent for Cancer Therapy |
title_full | Polyphenol Oxidase as a Promising Alternative Therapeutic Agent for Cancer Therapy |
title_fullStr | Polyphenol Oxidase as a Promising Alternative Therapeutic Agent for Cancer Therapy |
title_full_unstemmed | Polyphenol Oxidase as a Promising Alternative Therapeutic Agent for Cancer Therapy |
title_short | Polyphenol Oxidase as a Promising Alternative Therapeutic Agent for Cancer Therapy |
title_sort | polyphenol oxidase as a promising alternative therapeutic agent for cancer therapy |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8911857/ https://www.ncbi.nlm.nih.gov/pubmed/35268616 http://dx.doi.org/10.3390/molecules27051515 |
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