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Authors Sun R, Lu X, Gong L, Jin F
Received 19 August 2018
Accepted for publication 24 January 2019
Published 27 February 2019 Volume 2019:12 Pages 1641—1653
DOI https://doi.org/10.2147/OTT.S184555
Checked for plagiarism Yes
Review by Single-blind
Peer reviewers approved by Dr Colin Mak
Peer reviewer comments 2
Editor who approved publication: Dr Sanjeev Srivastava
Background: Lung
cancer is the most common and lethal malignancy worldwide. TCTP is highly
expressed in various cancers including lung cancer. Epithelial–mesenchymal
transition (EMT) could increase cancer cell invasion. Whether TCTP’s expression
is associated with EMT in lung adenocarcinoma is largely unknown.
Methods: Several
Gene Expression Omnibus datasets were used to analyze the correlation between
TCTP expression and overall survival of lung adenocarcinoma patients by
Kaplan–Meier survival analysis. Then, 24 surgically removed fresh lung
adenocarcinoma tissue samples and paired paracancer tissue samples were used to
analyze the correlation between TCTP expression and tumor stage by
immunohistochemical analysis. Furthermore, stable cell lines were generated
using lentiviral transduction systems to knock down or overexpress TCTP in A549
cells. Cell migration and invasion were measured by scratch and transwell
assays, and EMT marker proteins such as α-SMA, ZEB1, and E-cadherin were
quantitated by Western blot. The expression levels of miR-200a, miR-141, and
miR-429 were determined by real-time quantitative PCR, and their target genes
were predicted by an online database miRTarBase. The interaction between TCTP
and these genes was analyzed by String database and visualized by Cytoscape.
Results: TCTP was
highly expressed in tumor tissues compared to paracancer tissues. The
expression of TCTP was associated with shorter overall survival. TCTP knockdown
experiment in A549 cells suggested that TCTP knockdown could decrease the
migration and invasion of lung cancer cells, and the expression level of ZEB1
and α-SMA, but increase the expression of E-cadherin and p53. Vice versa,
overexpression of TCTP could increase the migration and invasion of cancer
cells, and the expression level of ZEB1 and α-SMA, but decrease the expression
of E-cadherin and p53. Furthermore, we found the expression of miR-200a,
miR-141, and miR-429 was associated with TCTP expression.
Conclusion: TCTP
promotes EMT in lung adenocarcinoma, and this effect may be associated with
miR-200 family members like miR-200a, miR-141, and miR-429.
Keywords: TCTP,
lung adenocarcinoma, epithelial–mesenchymal transition, miR-200