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  Efficient mining of anticancer peptides from gut metagenome

Ma, Y., Liu, X., Zhang, X., Yu, Y., Li, Y., Song, M., et al. (2023). Efficient mining of anticancer peptides from gut metagenome. Advanced Science, 10(25): 2300107. doi:10.1002/advs.202300107.

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 Creators:
Ma, Yue1, Author           
Liu, Xialin2, Author           
Zhang, Xuan, Author
Yu, Ying, Author
Li, Yujing, Author
Song, Moshi, Author
Wang, jun, Jun, Author
Affiliations:
1External Organizations, ou_persistent22              
2IMPRS for Evolutionary Biology, Max Planck Institute for Evolutionary Biology, Max Planck Society, ou_1445639              

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Free keywords: anticancer peptides, cancer therapy, gut microbiome, multi-center mining,tumour inhibitors
 Abstract: The gut microbiome plays a crucial role in modulating host health and disease. It serves as a vast reservoir of functional molecules that hold great potential for clinical applications. One specific area of interest is identifying anticancer peptides (ACPs) for innovative cancer therapies. However, ACPs discovery is hindered by a heavy reliance on experimental methodologies. To overcome this limitation, we here employed a novel approach by leveraging the overlap between ACPs and antimicrobial peptides (AMPs). By combining well-established AMP prediction methods with mining techniques in metagenomic cohorts, a total of 40 potential ACPs is identified. Out of the identified ACPs, 39 demonstrated inhibitory effects against at least one cancer cell line, exhibiting significant differences from known ACPs. Moreover, the therapeutic potential of the two most promising peptides in a mouse xenograft cancer model is evaluated. Encouragingly, the peptides exhibit effective tumor inhibition without any detectable toxic effects. Interestingly, both peptides display uncommon secondary structures, highlighting its distinctive characteristics. This findings highlight the efficacy of the multi-center mining approach, which effectively uncovers novel ACPs from the gut microbiome. This approach has significant implications for expanding treatment options not only for CRC, but also for other cancer types.

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Language(s): eng - English
 Dates: 2023-06-032023-01-052023-06-292023-09-05
 Publication Status: Issued
 Pages: -
 Publishing info: -
 Table of Contents: -
 Rev. Type: Peer
 Identifiers: DOI: 10.1002/advs.202300107
 Degree: -

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Project name : National Key Research and Development Program of China
Grant ID : 2021YFA0717000
Funding program : -
Funding organization : -
Project name : Strategic Priority Research Program of the Chinese Academy of Sciences
Grant ID : XDB29020000
Funding program : -
Funding organization : -
Project name : Program of the Beijing Natural Science Foundation
Grant ID : JQ22017
Funding program : -
Funding organization : -
Project name : Program of the Beijing Natural Science Foundation
Grant ID : JQ20031
Funding program : -
Funding organization : -
Project name : Beijing Nova Program
Grant ID : 202077
Funding program : -
Funding organization : -
Project name : Beijing Nova Program
Grant ID : 202120
Funding program : -
Funding organization : -
Project name : National Science Foundation of China
Grant ID : 81921006
Funding program : -
Funding organization : -
Project name : CAS Project for Young Scientists in Basic Research
Grant ID : YSBR-076
Funding program : -
Funding organization : -

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Title: Advanced Science
  Other : Adv. Sci.
Source Genre: Journal
 Creator(s):
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Publ. Info: Weinheim : Wiley-VCH
Pages: - Volume / Issue: 10 (25) Sequence Number: 2300107 Start / End Page: - Identifier: ISSN: 2198-3844
CoNE: https://pure.mpg.de/cone/journals/resource/2198-3844