Cargando…
AMTDB: A comprehensive database of autophagic modulators for anti-tumor drug discovery
Autophagy, originally described as a mechanism for intracellular waste disposal and recovery, has been becoming a crucial biological process closely related to many types of human tumors, including breast cancer, osteosarcoma, glioma, etc., suggesting that intervention of autophagy is a promising th...
Autores principales: | , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9395961/ https://www.ncbi.nlm.nih.gov/pubmed/36016573 http://dx.doi.org/10.3389/fphar.2022.956501 |
_version_ | 1784771820888522752 |
---|---|
author | Fu, Jiahui Wu, Lifeng Hu, Gaoyong Shi, Qiqi Wang, Ruodi Zhu, Lingjuan Yu, Haiyang Fu, Leilei |
author_facet | Fu, Jiahui Wu, Lifeng Hu, Gaoyong Shi, Qiqi Wang, Ruodi Zhu, Lingjuan Yu, Haiyang Fu, Leilei |
author_sort | Fu, Jiahui |
collection | PubMed |
description | Autophagy, originally described as a mechanism for intracellular waste disposal and recovery, has been becoming a crucial biological process closely related to many types of human tumors, including breast cancer, osteosarcoma, glioma, etc., suggesting that intervention of autophagy is a promising therapeutic strategy for cancer drug development. Therefore, a high-quality database is crucial for unraveling the complicated relationship between autophagy and human cancers, elucidating the crosstalk between the key autophagic pathways, and autophagic modulators with their remarkable antitumor activities. To achieve this goal, a comprehensive database of autophagic modulators (AMTDB) was developed. AMTDB focuses on 153 cancer types, 1,153 autophagic regulators, 860 targets, and 2,046 mechanisms/signaling pathways. In addition, a variety of classification methods, advanced retrieval, and target prediction functions are provided exclusively to cater to the different demands of users. Collectively, AMTDB is expected to serve as a powerful online resource to provide a new clue for the discovery of more candidate cancer drugs. |
format | Online Article Text |
id | pubmed-9395961 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-93959612022-08-24 AMTDB: A comprehensive database of autophagic modulators for anti-tumor drug discovery Fu, Jiahui Wu, Lifeng Hu, Gaoyong Shi, Qiqi Wang, Ruodi Zhu, Lingjuan Yu, Haiyang Fu, Leilei Front Pharmacol Pharmacology Autophagy, originally described as a mechanism for intracellular waste disposal and recovery, has been becoming a crucial biological process closely related to many types of human tumors, including breast cancer, osteosarcoma, glioma, etc., suggesting that intervention of autophagy is a promising therapeutic strategy for cancer drug development. Therefore, a high-quality database is crucial for unraveling the complicated relationship between autophagy and human cancers, elucidating the crosstalk between the key autophagic pathways, and autophagic modulators with their remarkable antitumor activities. To achieve this goal, a comprehensive database of autophagic modulators (AMTDB) was developed. AMTDB focuses on 153 cancer types, 1,153 autophagic regulators, 860 targets, and 2,046 mechanisms/signaling pathways. In addition, a variety of classification methods, advanced retrieval, and target prediction functions are provided exclusively to cater to the different demands of users. Collectively, AMTDB is expected to serve as a powerful online resource to provide a new clue for the discovery of more candidate cancer drugs. Frontiers Media S.A. 2022-08-09 /pmc/articles/PMC9395961/ /pubmed/36016573 http://dx.doi.org/10.3389/fphar.2022.956501 Text en Copyright © 2022 Fu, Wu, Hu, Shi, Wang, Zhu, Yu and Fu. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Pharmacology Fu, Jiahui Wu, Lifeng Hu, Gaoyong Shi, Qiqi Wang, Ruodi Zhu, Lingjuan Yu, Haiyang Fu, Leilei AMTDB: A comprehensive database of autophagic modulators for anti-tumor drug discovery |
title | AMTDB: A comprehensive database of autophagic modulators for anti-tumor drug discovery |
title_full | AMTDB: A comprehensive database of autophagic modulators for anti-tumor drug discovery |
title_fullStr | AMTDB: A comprehensive database of autophagic modulators for anti-tumor drug discovery |
title_full_unstemmed | AMTDB: A comprehensive database of autophagic modulators for anti-tumor drug discovery |
title_short | AMTDB: A comprehensive database of autophagic modulators for anti-tumor drug discovery |
title_sort | amtdb: a comprehensive database of autophagic modulators for anti-tumor drug discovery |
topic | Pharmacology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9395961/ https://www.ncbi.nlm.nih.gov/pubmed/36016573 http://dx.doi.org/10.3389/fphar.2022.956501 |
work_keys_str_mv | AT fujiahui amtdbacomprehensivedatabaseofautophagicmodulatorsforantitumordrugdiscovery AT wulifeng amtdbacomprehensivedatabaseofautophagicmodulatorsforantitumordrugdiscovery AT hugaoyong amtdbacomprehensivedatabaseofautophagicmodulatorsforantitumordrugdiscovery AT shiqiqi amtdbacomprehensivedatabaseofautophagicmodulatorsforantitumordrugdiscovery AT wangruodi amtdbacomprehensivedatabaseofautophagicmodulatorsforantitumordrugdiscovery AT zhulingjuan amtdbacomprehensivedatabaseofautophagicmodulatorsforantitumordrugdiscovery AT yuhaiyang amtdbacomprehensivedatabaseofautophagicmodulatorsforantitumordrugdiscovery AT fuleilei amtdbacomprehensivedatabaseofautophagicmodulatorsforantitumordrugdiscovery |