DIM-C-pPhtBu induces lysosomal dysfunction and unfolded protein response - mediated cell death via excessive mitophagy
DC Field | Value | Language |
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dc.contributor.author | Kang, Sung Un | - |
dc.contributor.author | Kim, Dae Ho | - |
dc.contributor.author | Lee, Yun Sang | - |
dc.contributor.author | Huang, Mei | - |
dc.contributor.author | Byeon, Hyung Kwon | - |
dc.contributor.author | Lee, Seong-Ho | - |
dc.contributor.author | Baek, Seung Joon | - |
dc.contributor.author | Kim, Chul-Ho | - |
dc.date.accessioned | 2021-09-10T05:49:15Z | - |
dc.date.available | 2021-09-10T05:49:15Z | - |
dc.date.issued | 2021-04-28 | - |
dc.identifier.issn | 0304-3835 | - |
dc.identifier.issn | 1872-7980 | - |
dc.identifier.uri | https://scholarworks.bwise.kr/sch/handle/2021.sw.sch/18894 | - |
dc.description.abstract | Despite technological advances in cancer treatment, the survival rate of patients with head and neck cancer (HNC) has not improved significantly. Many studies have shown that endoplasmic reticulum (ER) stress-related signals are associated with mitochondrial damage and that these signals determine whether cells maintain homeostasis or activate cell death programs. The unfolded protein response (UPR) is regulated by ER membrane proteins such as double-stranded RNA-activated protein kinase R(PKR)-like ER kinase (PERK), which directly activate transcription of chaperones or genes that function in redox homeostasis, protein secretion, or cell death programs. In this study, we focused on the role of mitophagy and ER stress-mediated cell death induced by DIMC-pPhtBu in HNC cancer. We found that DIM-C-pPhtBu, a compound that activates ER stress in many cancers, induced lysosomal dysfunction, excessive mitophagy, and cell death in HNC cells. Moreover, DIM-C-pPhtBu strongly inhibited HNC progression in a xenograft model by altering mitophagy related protein expression. Taken together, the results demonstrate that DIM-C-pPhtBu induces excessive mitophagy and eventually UPR-mediated cell death in HNC cells, suggesting that new anti-cancer drugs could be developed based on the connection between mitophagy and cancer cell death. | - |
dc.format.extent | 14 | - |
dc.language | 영어 | - |
dc.language.iso | ENG | - |
dc.publisher | Elsevier BV | - |
dc.title | DIM-C-pPhtBu induces lysosomal dysfunction and unfolded protein response - mediated cell death via excessive mitophagy | - |
dc.type | Article | - |
dc.publisher.location | 아일랜드 | - |
dc.identifier.doi | 10.1016/j.canlet.2021.01.005 | - |
dc.identifier.scopusid | 2-s2.0-85100732042 | - |
dc.identifier.wosid | 000625376500003 | - |
dc.identifier.bibliographicCitation | Cancer Letters, v.504, pp 23 - 36 | - |
dc.citation.title | Cancer Letters | - |
dc.citation.volume | 504 | - |
dc.citation.startPage | 23 | - |
dc.citation.endPage | 36 | - |
dc.type.docType | Article | - |
dc.description.isOpenAccess | N | - |
dc.description.journalRegisteredClass | scie | - |
dc.description.journalRegisteredClass | scopus | - |
dc.relation.journalResearchArea | Oncology | - |
dc.relation.journalWebOfScienceCategory | Oncology | - |
dc.subject.keywordPlus | AUTOPHAGY | - |
dc.subject.keywordPlus | HEAD | - |
dc.subject.keywordPlus | TRIGGERS | - |
dc.subject.keywordPlus | DEGRADATION | - |
dc.subject.keywordPlus | INVOLVEMENT | - |
dc.subject.keywordPlus | EXPRESSION | - |
dc.subject.keywordPlus | APOPTOSIS | - |
dc.subject.keywordPlus | P62 | - |
dc.subject.keywordPlus | NIX | - |
dc.subject.keywordAuthor | Differentially expressed genes (DEGs) | - |
dc.subject.keywordAuthor | Endoplasmic reticulum stress | - |
dc.subject.keywordAuthor | 3,3 '-diindolylmethane (DIM) | - |
dc.subject.keywordAuthor | Apoptosis-linked gene 2-interacting protein X (AIP1/Alix) | - |
dc.subject.keywordAuthor | Double-stranded RNA-Activated protein kinase-like ER kinase (PERK) | - |
dc.subject.keywordAuthor | HNC (Head and neck cancer) | - |
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