论文已发表
注册即可获取德孚的最新动态
IF 收录期刊
Authors Wang X, Lin M, Zhao J, Zhu S, Xu M, Zhou X
Received 12 March 2018
Accepted for publication 8 August 2018
Published 13 December 2018 Volume 2018:11 Pages 8815—8822
DOI https://doi.org/10.2147/OTT.S167902
Checked for plagiarism Yes
Review by Single-blind
Peer reviewers approved by Dr Justinn Cochran
Peer reviewer comments 2
Editor who approved publication: Dr Takuya Aoki
Purpose: To
explore the effects and mechanisms of tetraspanin TSPAN7 on the progression of
non-small-cell lung cancer (NSCLC) cells.
Patients and methods: All 125
lung cancer specimens and 60 metastatic tissues were obtained from patients
diagnosed with NSCLC, and we used immunohistochemistry to detect the expression
of TSPAN7 in NSCLC tissues and adjacent normal tissues. Cell proliferation and
invasion ability were determined by MTT, colony formation, and cell migration.
The relative protein expression level was analyzed by Western blot analysis.
Results: Our
clinical data showed that among 125 patients with lung cancer, TSPAN7 was
associated with lymph node status, differentiation, tumor size, and poor
prognosis. TSPAN7 knockout inhibited cell proliferation and migration. In
addition, TSPAN7 increased the expression of N-cadherin in NSCLC cells by
reducing the expression of E-cadherin and vimentin and promoting the cell
epithelial–mesenchymal transition (EMT) process. Xenograft transplantation
model confirmed the role of TSPAN7 in NSCLC metastasis.
Conclusion: TSPAN7-mediated
EMT is the key to NSCLC migration. TSPAN7 is a potential target for NSCLC
therapy.
Keywords: TSPAN7,
non-small-cell lung cancer, cell invasion, colony formation
