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Cellular Stress-Modulating Drugs Can Potentially Be Identified by in Silico Screening with Connectivity Map (CMap)
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dc.contributor.author Gao, Yu Rong -
dc.contributor.author Kim, Sung Woo -
dc.contributor.author Lee, Yun Il -
dc.contributor.author Lee, Jaemin -
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.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.identifier.bibliographicCitation Gao, Yu Rong. (2019-11). Cellular Stress-Modulating Drugs Can Potentially Be Identified by in Silico Screening with Connectivity Map (CMap). International Journal of Molecular Sciences, 20(22). doi: 10.3390/ijms20225601 -
dc.description.isOpenAccess TRUE -
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.citation.number 22 -
dc.citation.title International Journal of Molecular Sciences -
dc.citation.volume 20 -
dc.description.journalRegisteredClass scie -
dc.description.journalRegisteredClass scopus -
dc.relation.journalResearchArea Biochemistry & Molecular Biology; Chemistry -
dc.relation.journalWebOfScienceCategory Biochemistry & Molecular Biology; Chemistry, Multidisciplinary -
dc.type.docType Review -
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