Full metadata record
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Gao, Yu Rong | ko |
dc.contributor.author | Kim, Sung Woo | ko |
dc.contributor.author | Lee, Yun Il | ko |
dc.contributor.author | Lee, Jaemin | ko |
dc.date.accessioned | 2019-12-12T08:32:28Z | - |
dc.date.available | 2019-12-12T08:32:28Z | - |
dc.date.created | 2019-11-14 | - |
dc.date.issued | 2019-11 | - |
dc.identifier.citation | International Journal of Molecular Sciences, v.20, no.22 | - |
dc.identifier.issn | 1661-6596 | - |
dc.identifier.uri | http://hdl.handle.net/20.500.11750/10914 | - |
dc.description.abstract | Accompanied by increased life span, aging-associated diseases, such as metabolic diseases and cancers, have become serious health threats. Recent studies have documented that aging-associated diseases are caused by prolonged cellular stresses such as endoplasmic reticulum (ER) stress, mitochondrial stress, and oxidative stress. Thus, ameliorating cellular stresses could be an effective approach to treat aging-associated diseases and, more importantly, to prevent such diseases from happening. However, cellular stresses and their molecular responses within the cell are typically mediated by a variety of factors encompassing different signaling pathways. Therefore, a target-based drug discovery method currently being used widely (reverse pharmacology) may not be adequate to uncover novel drugs targeting cellular stresses and related diseases. The connectivity map (CMap) is an online pharmacogenomic database cataloging gene expression data from cultured cells treated individually with various chemicals, including a variety of phytochemicals. Moreover, by querying through CMap, researchers may screen registered chemicals in silico and obtain the likelihood of drugs showing a similar gene expression profile with desired and chemopreventive conditions. Thus, CMap is an effective genome-based tool to discover novel chemopreventive drugs. © 2019 by the authors. Licensee MDPI, Basel, Switzerland. | - |
dc.language | English | - |
dc.publisher | Multidisciplinary Digital Publishing Institute (MDPI) | - |
dc.title | Cellular Stress-Modulating Drugs Can Potentially Be Identified by in Silico Screening with Connectivity Map (CMap) | - |
dc.type | Article | - |
dc.identifier.doi | 10.3390/ijms20225601 | - |
dc.identifier.wosid | 000502786800083 | - |
dc.identifier.scopusid | 2-s2.0-85074771333 | - |
dc.type.local | Article(Overseas) | - |
dc.type.rims | ART | - |
dc.description.journalClass | 1 | - |
dc.identifier.citationVolume | 20 | - |
dc.identifier.citationNumber | 22 | - |
dc.identifier.citationTitle | International Journal of Molecular Sciences | - |
dc.type.journalArticle | Review | - |
dc.description.isOpenAccess | Y | - |
dc.subject.keywordAuthor | cellular stress | - |
dc.subject.keywordAuthor | endoplasmic reticulum stress | - |
dc.subject.keywordAuthor | ER stress | - |
dc.subject.keywordAuthor | mitochondrial stress | - |
dc.subject.keywordAuthor | oxidative stress | - |
dc.subject.keywordAuthor | hypoxia | - |
dc.subject.keywordAuthor | connectivity map | - |
dc.subject.keywordAuthor | CMap | - |
dc.subject.keywordAuthor | drug discovery | - |
dc.subject.keywordPlus | UNFOLDED PROTEIN RESPONSE | - |
dc.subject.keywordPlus | ENDOPLASMIC-RETICULUM STRESS | - |
dc.subject.keywordPlus | HEAT-SHOCK FACTOR-1 | - |
dc.subject.keywordPlus | TRANSCRIPTION FACTOR | - |
dc.subject.keywordPlus | GLUCOSE-HOMEOSTASIS | - |
dc.subject.keywordPlus | GENE-EXPRESSION | - |
dc.subject.keywordPlus | MESSENGER-RNA | - |
dc.subject.keywordPlus | ER STRESS | - |
dc.subject.keywordPlus | TRANSMEMBRANE PROTEIN | - |
dc.subject.keywordPlus | OXIDATIVE STRESS | - |
dc.contributor.affiliatedAuthor | Lee, Yun Il | - |
dc.contributor.affiliatedAuthor | Lee, Jaemin | - |