In Vivo and In Vitro Study on the Mechanism of Anticervical Cancer Effects of Corilagin in Mice.
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| Title: | In Vivo and In Vitro Study on the Mechanism of Anticervical Cancer Effects of Corilagin in Mice. |
|---|---|
| Authors: | Wang, Li-Mei1 (AUTHOR), Jiang, Yu-Han1 (AUTHOR), Li, Xing-Yu1 (AUTHOR), Wu, Min-Rui1 (AUTHOR), Xu, Zi-Yang1 (AUTHOR), Li, Long-Jie1 (AUTHOR), Yi, Yang2 (AUTHOR), Wang, Hong-Xun1 (AUTHOR) |
| Source: | Journal of Food Biochemistry. 5/13/2024, Vol. 2024, p1-14. 14p. |
| Subjects: | Ellagitannins, PI3K/AKT pathway, Inhibition of cellular proliferation, Cell cycle, Cervical cancer |
| Abstract: | Background. Corilagin has several pharmacological effects such as antitumor, anti-inflammatory, and cardiovascular disease treatment. Our previous studies have shown that the Corilagin can significantly inhibit proliferation of HeLa cells. However, there are no scientific data on the anticervical cancer effect of Corilagin in vivo. Methods. Network pharmacology was used to predict the mechanism, followed by in vitro experiments to detect cell proliferation, cycle, and apoptosis, and in vivo experiments to verify the mechanism. Results. It was speculated that the mechanism of action for the anticervical cancer of Corilagin could be related to PI3K/AKT and MAPK signaling pathways through network pharmacology. Results of cell assays in the present study showed that the Corilagin has significant effect on the proliferation, cell cycle, and apoptosis of murine cervical cancer U14 cells in vitro. In addition, Corilagin can significantly inhibit the growth of U14 tumor-bearing mice with insignificant toxic effect on the liver and kidney of the transplanted mice. The current study found that Corilagin can delay development of cervical cancer by boosting antitumor immune responses of the body. RT-PCR and Western blotting were applied in the current study to evident that Corilagin can achieve anticervical cancer property by inducing apoptosis of tumor tissues through both PI3K/AKT and MAPK signaling pathways. Conclusion. Therefore, this study provided theoretical reference for research of Corilagin as a bioresource for development of an anticervical cancer drug and functional food. [ABSTRACT FROM AUTHOR] |
| Copyright of Journal of Food Biochemistry is the property of Wiley-Blackwell and its content may not be copied or emailed to multiple sites without the copyright holder's express written permission. Additionally, content may not be used with any artificial intelligence tools or machine learning technologies. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.) | |
| Database: | Engineering Source |
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| Header | DbId: egs DbLabel: Engineering Source An: 177291166 AccessLevel: 6 PubType: Academic Journal PubTypeId: academicJournal PreciseRelevancyScore: 0 |
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| Items | – Name: Title Label: Title Group: Ti Data: In Vivo and In Vitro Study on the Mechanism of Anticervical Cancer Effects of Corilagin in Mice. – Name: Author Label: Authors Group: Au Data: <searchLink fieldCode="AR" term="%22Wang%2C+Li-Mei%22">Wang, Li-Mei</searchLink><relatesTo>1</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Jiang%2C+Yu-Han%22">Jiang, Yu-Han</searchLink><relatesTo>1</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Li%2C+Xing-Yu%22">Li, Xing-Yu</searchLink><relatesTo>1</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Wu%2C+Min-Rui%22">Wu, Min-Rui</searchLink><relatesTo>1</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Xu%2C+Zi-Yang%22">Xu, Zi-Yang</searchLink><relatesTo>1</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Li%2C+Long-Jie%22">Li, Long-Jie</searchLink><relatesTo>1</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Yi%2C+Yang%22">Yi, Yang</searchLink><relatesTo>2</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Wang%2C+Hong-Xun%22">Wang, Hong-Xun</searchLink><relatesTo>1</relatesTo> (AUTHOR) – Name: TitleSource Label: Source Group: Src Data: <searchLink fieldCode="JN" term="%22Journal+of+Food+Biochemistry%22">Journal of Food Biochemistry</searchLink>. 5/13/2024, Vol. 2024, p1-14. 14p. – Name: Subject Label: Subjects Group: Su Data: <searchLink fieldCode="DE" term="%22Ellagitannins%22">Ellagitannins</searchLink><br /><searchLink fieldCode="DE" term="%22PI3K%2FAKT+pathway%22">PI3K/AKT pathway</searchLink><br /><searchLink fieldCode="DE" term="%22Inhibition+of+cellular+proliferation%22">Inhibition of cellular proliferation</searchLink><br /><searchLink fieldCode="DE" term="%22Cell+cycle%22">Cell cycle</searchLink><br /><searchLink fieldCode="DE" term="%22Cervical+cancer%22">Cervical cancer</searchLink> – Name: Abstract Label: Abstract Group: Ab Data: Background. Corilagin has several pharmacological effects such as antitumor, anti-inflammatory, and cardiovascular disease treatment. Our previous studies have shown that the Corilagin can significantly inhibit proliferation of HeLa cells. However, there are no scientific data on the anticervical cancer effect of Corilagin in vivo. Methods. Network pharmacology was used to predict the mechanism, followed by in vitro experiments to detect cell proliferation, cycle, and apoptosis, and in vivo experiments to verify the mechanism. Results. It was speculated that the mechanism of action for the anticervical cancer of Corilagin could be related to PI3K/AKT and MAPK signaling pathways through network pharmacology. Results of cell assays in the present study showed that the Corilagin has significant effect on the proliferation, cell cycle, and apoptosis of murine cervical cancer U14 cells in vitro. In addition, Corilagin can significantly inhibit the growth of U14 tumor-bearing mice with insignificant toxic effect on the liver and kidney of the transplanted mice. The current study found that Corilagin can delay development of cervical cancer by boosting antitumor immune responses of the body. RT-PCR and Western blotting were applied in the current study to evident that Corilagin can achieve anticervical cancer property by inducing apoptosis of tumor tissues through both PI3K/AKT and MAPK signaling pathways. Conclusion. Therefore, this study provided theoretical reference for research of Corilagin as a bioresource for development of an anticervical cancer drug and functional food. [ABSTRACT FROM AUTHOR] – Name: AbstractSuppliedCopyright Label: Group: Ab Data: <i>Copyright of Journal of Food Biochemistry is the property of Wiley-Blackwell and its content may not be copied or emailed to multiple sites without the copyright holder's express written permission. Additionally, content may not be used with any artificial intelligence tools or machine learning technologies. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract.</i> (Copyright applies to all Abstracts.) |
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| RecordInfo | BibRecord: BibEntity: Identifiers: – Type: doi Value: 10.1155/2024/4822900 Languages: – Code: eng Text: English PhysicalDescription: Pagination: PageCount: 14 StartPage: 1 Subjects: – SubjectFull: Ellagitannins Type: general – SubjectFull: PI3K/AKT pathway Type: general – SubjectFull: Inhibition of cellular proliferation Type: general – SubjectFull: Cell cycle Type: general – SubjectFull: Cervical cancer Type: general Titles: – TitleFull: In Vivo and In Vitro Study on the Mechanism of Anticervical Cancer Effects of Corilagin in Mice. Type: main BibRelationships: HasContributorRelationships: – PersonEntity: Name: NameFull: Wang, Li-Mei – PersonEntity: Name: NameFull: Jiang, Yu-Han – PersonEntity: Name: NameFull: Li, Xing-Yu – PersonEntity: Name: NameFull: Wu, Min-Rui – PersonEntity: Name: NameFull: Xu, Zi-Yang – PersonEntity: Name: NameFull: Li, Long-Jie – PersonEntity: Name: NameFull: Yi, Yang – PersonEntity: Name: NameFull: Wang, Hong-Xun IsPartOfRelationships: – BibEntity: Dates: – D: 13 M: 05 Text: 5/13/2024 Type: published Y: 2024 Identifiers: – Type: issn-print Value: 01458884 Numbering: – Type: volume Value: 2024 Titles: – TitleFull: Journal of Food Biochemistry Type: main |
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