Expression of ADAM33 Is a Novel Regulatory Mechanism in IL-18-Secreted Process in Gastric Cancer
- Authors
- Kim, Kyung-Eun; Song, Hyunkeun; Hahm, Candace; Yoon, Sun Young; Park, Sunyoung; Lee, Ha-reum; Hur, Dae Young; Kim, Taesung; Kim, Cherl-hyun; Bang, Sa Ik; Bang, Jung-Wook; Park, Hyunjeong; Cho, Dae-Ho
- Issue Date
- Mar-2009
- Publisher
- AMER ASSOC IMMUNOLOGISTS
- Citation
- JOURNAL OF IMMUNOLOGY, v.182, no.6, pp 3548 - 3555
- Pages
- 8
- Journal Title
- JOURNAL OF IMMUNOLOGY
- Volume
- 182
- Number
- 6
- Start Page
- 3548
- End Page
- 3555
- URI
- https://scholarworks.sookmyung.ac.kr/handle/2020.sw.sookmyung/13803
- DOI
- 10.4049/jimmunol.0801695
- ISSN
- 0022-1767
1550-6606
- Abstract
- IL-18 has recently been reported to play a critical role in tumor migration, invasion, and metastasis. Because IL-18 has various biological activities after its secretion as an 18 kDa mature form, the regulation of the IL-18 secretion process is an important step in tumor progression. This study investigated the implication of IL-18 in vascular endothelial growth factor (VEGF)-D-regulated migration, along with the role of the IL-18 secretion process. VEGF-D enhanced cell migration, which was then blocked by inhibiting IL-18. VEGF-D increased 11,48 expression and secretion, suggesting that IL-18 is a critical mediator for VEGF-D-enhanced migration. VEGF-D induced a disintegrin and metalloprotease 33 (ADAM33) expression, which has a metalloproteinase domain. VEGF-D-enhanced IL-18 secretion and cell migration were inhibited by ADAM33 knock-down. Moreover, cell proliferation was considerably reduced in ADAM33 small interfering RNA transfectants. In conclusion, ADAM33 has a key role in gastric cancer pathogenesis by up-regulating IL-18 secretion process, resulting in increased cell migration and proliferation. The Journal of Immunology, 2009, 182: 3548-3555.
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Collections - 대학 > 기초교양대학 > 기초교양학부 > 1. Journal Articles
- 원격대학원 > 향장미용학과 > 1. Journal Articles
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