Background
In present study, we explored the function of the metastasis-associated lung adenocarcinoma transcript 1 (
MALAT1
) gene in the development of non-small cell lung cancer (NSCLC).
Material/Methods
qRT-PCR was used to detect the
MALAT1
mRNA expression level in cancer tissues and adjacent normal tissues of 115 NSCLC patients and in cell lines.
MALAT1
-mimic,
MALAT1
-inhibitor, and corresponding negative controls (NC) were utilized to transfect the H460 cells. Proliferation, migration, and invasion of H460 cells were evaluated by MTT method and Transwell assay. Expression levels of proteins in the ERK/MAPK signaling pathway were assessed by Western blot analysis.
Results
MALAT1
mRNA was upregulated in NSCLC tissues and cell lines compared to that in adjacent tissues and normal human bronchial cell line (BEAS-2B), respectively. Overexpression of
MALAT1
significantly strengthened the proliferation, migration, and invasion ability of H460 cells. In comparison with the NC group, expression levels of
CXCL5
and p-
JNK
proteins were elevated, while p-
MAPK
and p-
ERK
proteins were decreased in the
MALAT1
-mimic group.
MALAT1
targets the 3′-untranslated region (UTR) fragment of the
CXCL5
gene and inhibits its translation. Disturbance of the
CXCL5
gene can reduce the protein expression of
MAPK
, p-
MEK
1/2, p-
ERK1/2,
and p-
JNK
, and inhibit the proliferation, migration, and invasion of
MALAT1
-mimic cells.
Conclusions
High
MALAT1
expression promotes the proliferation, migration, and invasion of non-small cell lung cancer via the ERK/MAPK signaling pathway.