Cited 0 time in
Up-regulation of RhoGDI2 in Human Breast Cancer and Its Prognostic Implications
| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | Moon, Hyeong-Gon | - |
| dc.contributor.author | Jeong, Sang-Ho | - |
| dc.contributor.author | Ju, Young-Tae | - |
| dc.contributor.author | Jeong, Chi-Young | - |
| dc.contributor.author | Lee, Jong Sil | - |
| dc.contributor.author | Lee, Young-Joon | - |
| dc.contributor.author | Hong, Soon-Chan | - |
| dc.contributor.author | Choi, Sang-Kyung | - |
| dc.contributor.author | Ha, Woo-Song | - |
| dc.contributor.author | Park, Soon-Tae | - |
| dc.contributor.author | Jung, Eun-Jung | - |
| dc.date.accessioned | 2022-12-27T04:06:44Z | - |
| dc.date.available | 2022-12-27T04:06:44Z | - |
| dc.date.issued | 2010-09 | - |
| dc.identifier.issn | 1598-2998 | - |
| dc.identifier.issn | 2005-9256 | - |
| dc.identifier.uri | https://scholarworks.gnu.ac.kr/handle/sw.gnu/24965 | - |
| dc.description.abstract | Purpose Recent research has identified many genes and proteins that play specific roles in the process of systemic metastasis in various types of cancer. Rho GDP dissociation inhibitor 2 (RhoGDI2) has been shown to inhibit metastasis in human bladder cancer, but its role in breast cancer is controversial. Materials and Methods We examined the regulation and clinical significance of RhoGDI2 in Korean breast cancer patients by using proteomic approaches. Results By using a proteomic approach, we observed an increased expression of RhoGDI2 in human breast cancer tissues when compared to that of the normal breast tissues, and we validated its up-regulation in an independent cohort of 8 breast cancer patients. The clinical implication of a RhoGDI2 expression was investigated in 57 breast cancer patients by performing immunohistochemistry. RhoGDI2 did not show a significant association with the tumor size, lymph node metastasis, the histologic grade or the hormone receptor status. However, the patients with RhoGDI2-expressing tumors had significantly shorter disease-free survival (p=0.043; hazard ratio, 3.87) and distant metastasis-free survival (p=0.039; hazard ratio, 5.15). Conclusion Our results demonstrated a potential role of RhoGDI2 as a poor prognostic marker as well as a potential therapeutic target. The pro-metastatic nature of RhoGDI2 shown in our study may indicate its organ-specific role in cancer metastasis. | - |
| dc.format.extent | 6 | - |
| dc.language | 영어 | - |
| dc.language.iso | ENG | - |
| dc.publisher | 대한암학회 | - |
| dc.title | Up-regulation of RhoGDI2 in Human Breast Cancer and Its Prognostic Implications | - |
| dc.type | Article | - |
| dc.publisher.location | 대한민국 | - |
| dc.identifier.doi | 10.4143/crt.2010.42.3.151 | - |
| dc.identifier.wosid | 000208488000005 | - |
| dc.identifier.bibliographicCitation | Cancer Research and Treatment, v.42, no.3, pp 151 - 156 | - |
| dc.citation.title | Cancer Research and Treatment | - |
| dc.citation.volume | 42 | - |
| dc.citation.number | 3 | - |
| dc.citation.startPage | 151 | - |
| dc.citation.endPage | 156 | - |
| dc.type.docType | Article | - |
| dc.identifier.kciid | ART001480753 | - |
| dc.description.isOpenAccess | N | - |
| dc.description.journalRegisteredClass | kci | - |
| dc.relation.journalResearchArea | Oncology | - |
| dc.relation.journalWebOfScienceCategory | Oncology | - |
| dc.subject.keywordAuthor | Breast neoplasms | - |
| dc.subject.keywordAuthor | RhoGDI2 protein | - |
| dc.subject.keywordAuthor | Prognosis | - |
| dc.subject.keywordAuthor | Neoplasm metastasis | - |
| dc.subject.keywordAuthor | Proteomics | - |
Items in ScholarWorks are protected by copyright, with all rights reserved, unless otherwise indicated.
Gyeongsang National University Central Library, 501, Jinju-daero, Jinju-si, Gyeongsangnam-do, 52828, Republic of Korea+82-55-772-0532
COPYRIGHT 2022 GYEONGSANG NATIONAL UNIVERSITY LIBRARY. 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.
