Dexamethasone Inhibits TGF-beta 1-Induced Cell Migration by Regulating the ERK and AKT Pathways in Human Colon Cancer Cells Via CYR61
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Han, Sanghoon | - |
dc.contributor.author | Ngoc Thuy Bui | - |
dc.contributor.author | Manh Tin Ho | - |
dc.contributor.author | Kim, Young Mee | - |
dc.contributor.author | Cho, Moonjae | - |
dc.contributor.author | Shin, Dong Bok | - |
dc.date.available | 2020-02-28T01:43:37Z | - |
dc.date.created | 2020-02-06 | - |
dc.date.issued | 2016-07 | - |
dc.identifier.issn | 1598-2998 | - |
dc.identifier.uri | https://scholarworks.bwise.kr/gachon/handle/2020.sw.gachon/8151 | - |
dc.description.abstract | Purpose One of the features in cancer development is the migration of cancer cells to form metastatic lesions. CYR61 protein promotes migration and the epithelial-mesenchymal transition in several cancer cell types. Evidence suggests that CYR61 and dexamethasone are relevant to colorectal cancer. However, relationships between them and colorectal cancer are still unclear. Understanding the molecular mechanism of colorectal cancer progression related with CYR61 and dexamethasone, which is widely used for combination chemotherapy, is necessary for improved therapy. Materials and Methods We used colorectal cancer cells, HCT116, co-treated with transforming growth factor beta 1 (TGF-beta 1) and dexamethasone to examine the inhibitory migration effect of dexamethasone by migratory assay. Alternatively, both migratory pathways, expression of AKT and ERK, and the target factor CYR61 was also tested by co-treatment with TGF-beta 1 and dexamethasone. Results We report that dexamethasone significantly inhibited TGF-beta 1-induced cell migration, without affecting cell proliferation. Importantly, we observed that TGF-beta 1 promoted the epithelial-mesenchymal transition process and that dexamethasone co-treatment abolished this effect. ERK and AKT signaling pathways were found to mediate TGF-beta 1-induced migration, which was inhibited by dexamethasone. In addition, TGF-beta 1 treatment induced CYR61 expression whereas dexamethasone reduced it. These observations were compatible with the modulation of migration observed following treatment of HCT116 cells with human recombinant CYR61 and anti-CYR61 antibody. Our results also indicated that TGF-beta 1 enhanced collagen I and reduced matrix metalloproteinase 1 expression, which was reversed by dexamethasone treatment. Conclusion These findings suggested that dexamethasone inhibits AKT and ERK phosphorylation, leading to decreased CYR61 expression, which in turn blocks TGF-beta 1-induced migration. | - |
dc.language | 영어 | - |
dc.language.iso | en | - |
dc.publisher | KOREAN CANCER ASSOCIATION | - |
dc.relation.isPartOf | CANCER RESEARCH AND TREATMENT | - |
dc.subject | EPITHELIAL-MESENCHYMAL TRANSITION | - |
dc.subject | COLORECTAL-CANCER | - |
dc.subject | PROSTATE-CANCER | - |
dc.subject | TUMOR-GROWTH | - |
dc.subject | PROTEIN | - |
dc.subject | GLUCOCORTICOIDS | - |
dc.subject | CARBOPLATIN | - |
dc.subject | METASTASIS | - |
dc.subject | EXPRESSION | - |
dc.subject | SURVIVAL | - |
dc.title | Dexamethasone Inhibits TGF-beta 1-Induced Cell Migration by Regulating the ERK and AKT Pathways in Human Colon Cancer Cells Via CYR61 | - |
dc.type | Article | - |
dc.type.rims | ART | - |
dc.description.journalClass | 1 | - |
dc.identifier.wosid | 000380496900030 | - |
dc.identifier.doi | 10.4143/crt.2015.209 | - |
dc.identifier.bibliographicCitation | CANCER RESEARCH AND TREATMENT, v.48, no.3, pp.1141 - 1153 | - |
dc.identifier.kciid | ART002127490 | - |
dc.identifier.scopusid | 2-s2.0-84981321233 | - |
dc.citation.endPage | 1153 | - |
dc.citation.startPage | 1141 | - |
dc.citation.title | CANCER RESEARCH AND TREATMENT | - |
dc.citation.volume | 48 | - |
dc.citation.number | 3 | - |
dc.contributor.affiliatedAuthor | Shin, Dong Bok | - |
dc.type.docType | Article | - |
dc.subject.keywordAuthor | Cysteine-rich protein 61 | - |
dc.subject.keywordAuthor | Dexamethasone | - |
dc.subject.keywordAuthor | Colon | - |
dc.subject.keywordPlus | EPITHELIAL-MESENCHYMAL TRANSITION | - |
dc.subject.keywordPlus | COLORECTAL-CANCER | - |
dc.subject.keywordPlus | PROSTATE-CANCER | - |
dc.subject.keywordPlus | TUMOR-GROWTH | - |
dc.subject.keywordPlus | PROTEIN | - |
dc.subject.keywordPlus | GLUCOCORTICOIDS | - |
dc.subject.keywordPlus | CARBOPLATIN | - |
dc.subject.keywordPlus | METASTASIS | - |
dc.subject.keywordPlus | EXPRESSION | - |
dc.subject.keywordPlus | SURVIVAL | - |
dc.relation.journalResearchArea | Oncology | - |
dc.relation.journalWebOfScienceCategory | Oncology | - |
dc.description.journalRegisteredClass | scie | - |
dc.description.journalRegisteredClass | scopus | - |
dc.description.journalRegisteredClass | kci | - |
Items in ScholarWorks are protected by copyright, with all rights reserved, unless otherwise indicated.
1342, Seongnam-daero, Sujeong-gu, Seongnam-si, Gyeonggi-do, Republic of Korea(13120)031-750-5114
COPYRIGHT 2020 Gachon University All Rights Reserved.
Certain data included herein are derived from the © Web of Science of Clarivate Analytics. All rights reserved.
You may not copy or re-distribute this material in whole or in part without the prior written consent of Clarivate Analytics.