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Weipixiao attenuate early angiogenesis in rats with gastric precancerous lesions

BACKGROUND: Angiogenesis is a pathobiological hallmark of gastric cancer. However, rare studies focus on angiogenesis in gastric precancerous lesions (GPL). Weipixiao (WPX), a Chinese herbal preparation, is proved clinically effective in treating GPL. Here, we evaluated WPX’s anti-angiogenic potenti...

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Autores principales: Zeng, Jinhao, Yan, Ran, Pan, Huafeng, You, Fengming, Cai, Tiantian, Liu, Wei, Zheng, Chuan, Zhao, Ziming, Gong, Daoyin, Chen, Longhui, Zhang, Yi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6131880/
https://www.ncbi.nlm.nih.gov/pubmed/30200948
http://dx.doi.org/10.1186/s12906-018-2309-3
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author Zeng, Jinhao
Yan, Ran
Pan, Huafeng
You, Fengming
Cai, Tiantian
Liu, Wei
Zheng, Chuan
Zhao, Ziming
Gong, Daoyin
Chen, Longhui
Zhang, Yi
author_facet Zeng, Jinhao
Yan, Ran
Pan, Huafeng
You, Fengming
Cai, Tiantian
Liu, Wei
Zheng, Chuan
Zhao, Ziming
Gong, Daoyin
Chen, Longhui
Zhang, Yi
author_sort Zeng, Jinhao
collection PubMed
description BACKGROUND: Angiogenesis is a pathobiological hallmark of gastric cancer. However, rare studies focus on angiogenesis in gastric precancerous lesions (GPL). Weipixiao (WPX), a Chinese herbal preparation, is proved clinically effective in treating GPL. Here, we evaluated WPX’s anti-angiogenic potential for GPL, and also investigated the possibility of its anti-angiogenic mechanisms. METHODS: HPLC analysis was applied to screen the major chemical components of WPX. After modeling N-methyl-N′-nitro-N-nitrosoguanidine (MNNG)-induced GPL in male Sprague-Dawley rats, different doses of WPX were administrated orally for 10 weeks. Next, we performed histopathological examination using routine H&E staining and HID-AB-PAS staining. In parallel, we assessed angiogenesis revealed by microvessel density (MVD) using CD34 immunostaining, and subsequently observe microvessel ultrastructure in gastric mucosa under Transmission Electron Microscope. Finally, we detect expression of angiogenesis-associated markers VEGF and HIF-1α using immunohistochemistry. Moreover, mRNA expressions of ERK1, ERK2, Cylin D1 as well as HIF-1α in gastric mucosa were determined by quantitative real-time reverse transcription- polymerase chain reaction. RESULTS: We observed the appearance of active angiogenesis in GPL rats, and demonstrated that WPX could reduce microvascular abnormalities and attenuate early angiogenesis in most of GPL specimens with a concomitant regression of most intestinal metaplasia (IM) and a portion of gastric epithelial dysplasia (GED). In parallel, WPX could suppress HIF-1α mRNA expression (P < 0.01) as well as protein expression (although without statistical significance), and could markedly inhibit VEGF protein expression in GPL rats. Mechanistically, WPX intervention, especially at low dose, caused a significant decrease in the ERK1 and Cylin D1 mRNA levels. However, WPX might probably have no regulatory effect on ERK2 amplification. CONCLUSIONS: WPX could attenuate early angiogenesis and temper microvascular abnormalities in GPL rats. This might be partly achieved by inhibiting on the angiogenesis-associated markers HIF-1α and VEGF, and on the ERK1/Cylin D1 aberrant activation. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12906-018-2309-3) contains supplementary material, which is available to authorized users.
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spelling pubmed-61318802018-09-13 Weipixiao attenuate early angiogenesis in rats with gastric precancerous lesions Zeng, Jinhao Yan, Ran Pan, Huafeng You, Fengming Cai, Tiantian Liu, Wei Zheng, Chuan Zhao, Ziming Gong, Daoyin Chen, Longhui Zhang, Yi BMC Complement Altern Med Research Article BACKGROUND: Angiogenesis is a pathobiological hallmark of gastric cancer. However, rare studies focus on angiogenesis in gastric precancerous lesions (GPL). Weipixiao (WPX), a Chinese herbal preparation, is proved clinically effective in treating GPL. Here, we evaluated WPX’s anti-angiogenic potential for GPL, and also investigated the possibility of its anti-angiogenic mechanisms. METHODS: HPLC analysis was applied to screen the major chemical components of WPX. After modeling N-methyl-N′-nitro-N-nitrosoguanidine (MNNG)-induced GPL in male Sprague-Dawley rats, different doses of WPX were administrated orally for 10 weeks. Next, we performed histopathological examination using routine H&E staining and HID-AB-PAS staining. In parallel, we assessed angiogenesis revealed by microvessel density (MVD) using CD34 immunostaining, and subsequently observe microvessel ultrastructure in gastric mucosa under Transmission Electron Microscope. Finally, we detect expression of angiogenesis-associated markers VEGF and HIF-1α using immunohistochemistry. Moreover, mRNA expressions of ERK1, ERK2, Cylin D1 as well as HIF-1α in gastric mucosa were determined by quantitative real-time reverse transcription- polymerase chain reaction. RESULTS: We observed the appearance of active angiogenesis in GPL rats, and demonstrated that WPX could reduce microvascular abnormalities and attenuate early angiogenesis in most of GPL specimens with a concomitant regression of most intestinal metaplasia (IM) and a portion of gastric epithelial dysplasia (GED). In parallel, WPX could suppress HIF-1α mRNA expression (P < 0.01) as well as protein expression (although without statistical significance), and could markedly inhibit VEGF protein expression in GPL rats. Mechanistically, WPX intervention, especially at low dose, caused a significant decrease in the ERK1 and Cylin D1 mRNA levels. However, WPX might probably have no regulatory effect on ERK2 amplification. CONCLUSIONS: WPX could attenuate early angiogenesis and temper microvascular abnormalities in GPL rats. This might be partly achieved by inhibiting on the angiogenesis-associated markers HIF-1α and VEGF, and on the ERK1/Cylin D1 aberrant activation. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12906-018-2309-3) contains supplementary material, which is available to authorized users. BioMed Central 2018-09-10 /pmc/articles/PMC6131880/ /pubmed/30200948 http://dx.doi.org/10.1186/s12906-018-2309-3 Text en © The Author(s). 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Zeng, Jinhao
Yan, Ran
Pan, Huafeng
You, Fengming
Cai, Tiantian
Liu, Wei
Zheng, Chuan
Zhao, Ziming
Gong, Daoyin
Chen, Longhui
Zhang, Yi
Weipixiao attenuate early angiogenesis in rats with gastric precancerous lesions
title Weipixiao attenuate early angiogenesis in rats with gastric precancerous lesions
title_full Weipixiao attenuate early angiogenesis in rats with gastric precancerous lesions
title_fullStr Weipixiao attenuate early angiogenesis in rats with gastric precancerous lesions
title_full_unstemmed Weipixiao attenuate early angiogenesis in rats with gastric precancerous lesions
title_short Weipixiao attenuate early angiogenesis in rats with gastric precancerous lesions
title_sort weipixiao attenuate early angiogenesis in rats with gastric precancerous lesions
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6131880/
https://www.ncbi.nlm.nih.gov/pubmed/30200948
http://dx.doi.org/10.1186/s12906-018-2309-3
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