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Kim, Hongtae
Cancer/DNA damage Lab.
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Overexpression of a novel regulator of p120 catenin, NLBP, promotes lung adenocarcinoma proliferation

Author(s)
Kim, Chang HeeNam, Hae-SeongLee, Eun HeeHan, Seung HunCho, Hyun JungChung, Hee JinLee, Nam SooChoi, Suk JinKim, HojoongRyu, Jeong SeonKwon, JunhyeKim, Hongtae
Issued Date
2013-08
DOI
10.4161/cc.25451
URI
https://scholarworks.unist.ac.kr/handle/201301/24891
Fulltext
https://www.tandfonline.com/doi/abs/10.4161/cc.25451
Citation
CELL CYCLE, v.12, no.15, pp.2443 - 2453
Abstract
NLBP (novel LZAP-binding protein) was recently shown to function as a tumor suppressor capable of inhibiting the NFB signaling pathway. NLBP is also known as a negative regulator of cell invasion, and its expression is reduced in several cancer cell lines that have little invasive activity. Although these phenomena suggest that NLBP may be a potential tumor suppressor, its role as a tumor suppressor in human lung cancer is not well established. In contrast to our expectation, NLBP was highly expressed in the early stage of lung adenocarcinoma tissues, and overexpression of NLBP promoted proliferation of H1299 lung adenocarcinoma cells. We also found that p120 catenin (p120ctn) was a novel binding partner of NLBP, and that NLBP binds to the regulatory domain of p120ctn, and p120ctn associates with N-terminal region of NLBP, respectively. This binding leads to p120ctn stability to inhibit proteasomal degradation of p120ctn by inhibiting its ubiqutination. In addition, we also found that overexpression of NLBP and p120ctn in human lung cancer are closely related with adenocarcinoma compared with squamous cell carcinoma. Taken together, our findings reveal that NLBP is highly overexpressed in human lung adenocarcinoma, and that overexpression of NLBP promotes the cell proliferation of lung adenocarcinoma through interacting with p120ctn and suggest that NLBP may function as an oncogene in early stage carcinogenesis of lung adenocarcinoma.
Publisher
TAYLOR & FRANCIS INC
ISSN
1538-4101
Keyword (Author)
cell proliferationNLBPp120 cateninubiquitinationcancer
Keyword
RHO-FAMILY GTPASESBETA-CATENINCANCERPROTEININVASIONWNTMECHANISMSEXPRESSIONSURVIVALTUMORS

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