Integrin alpha 6: A novel therapeutic target in esophageal squamous cell carcinoma
- Authors
- Kwon, Junhye; Lee, Tae-Sup; Lee, Hae Won; Kang, Moon Chul; Yoon, Hyeon-Joon; Kim, Ji-Hee; Park, Jong Ho
- Issue Date
- Nov-2013
- Publisher
- SPANDIDOS PUBL LTD
- Keywords
- esophageal squamous cell carcinoma; integrin alpha 6; tumorigenesis; biodistribution; xenograft model
- Citation
- INTERNATIONAL JOURNAL OF ONCOLOGY, v.43, no.5, pp.1523 - 1530
- Journal Title
- INTERNATIONAL JOURNAL OF ONCOLOGY
- Volume
- 43
- Number
- 5
- Start Page
- 1523
- End Page
- 1530
- URI
- https://scholarworks.sookmyung.ac.kr/handle/2020.sw.sookmyung/11195
- DOI
- 10.3892/ijo.2013.2097
- ISSN
- 1019-6439
- Abstract
- Esophageal squamous cell carcinoma (ESCC), the most common subtype of esophageal cancer in East Asian countries, is a devastating disease characterized by distinctly high incidence and mortality rates. Our previous expression profile analysis showed that integrin alpha 6 (ITGA6) is highly expressed in ESCC tissues. To validate cell surface expression of ITGA6 as a novel target in ESCC, we investigated ITGA6 expression in tumor tissue samples and cell lines of ESCC and found that ITGA6 was upregulated in these cells. In vitro knockdown of ITGA6 in ESCC cells resulted in inhibition of cell proliferation, invasion and colony formation. In addition, we demonstrated that ITGA6 associates with integrin beta 4 (ITGB4), and that this heterodimer complex is upregulated in both ESCC tissues and cell lines. Moreover, our biodistribution results in an ESCC xenograft model indicated that ITGA6 is a possible target for antibody-related diagnostic and therapeutic modalities in ESCC. Thus, our findings suggest that ITGA6 plays an important role in tumorigenesis in ESCC and represents a potential therapeutic target in the treatment of ESCC.
- Files in This Item
- There are no files associated with this item.
- Appears in
Collections - 이과대학 > 생명시스템학부 > 1. Journal Articles

Items in ScholarWorks are protected by copyright, with all rights reserved, unless otherwise indicated.