[No authors listed]
A previous study indicated that LIM domain containing 2 (LIMD2) is an oncogene in a variety of human cancers, including breast, bladder and thyroid cancers, and melanoma; however, the role of LIMD2 in nonâsmall cell lung cancer (NSCLC) remains largely unknown. In the present study, by reverse transcriptionâquantitative polymerase chain reaction (RTâqPCR) analysis, it was demonstrated that LIMD2 was significantly upregulated in NSCLC tissues compared with adjacent normal tissues. Consistently, LIMD2 was also upregulated in NSCLC cell lines. Furthermore, the present study reported that knockdown of LIMD2 significantly inhibited the proliferation and invasion of H1299 and A549 cells by Cell Counting Kitâ8 and Transwell assays. In addition, the expression of LIMD2 was determined to be regulated by microRNA (miR)â34a in the present study. RTâqPCR and western blot analysis indicated that overexpression of miRâ34a notably reduced the mRNA and protein expression levels of LIMD2 in H1299 and H549 cells. Additionally, the present study reported an inverse correlation between the expression of LIMD2 and miRâ34a in NSCLC tissues. A luciferase reporter assay also demonstrated that miRâ34a directly targeted the mRNA expression of LIMD2 in NSCLC cells. Finally, miRâ34a was revealed to possess a tumor suppressive role in NSCLC cells. Collectively, the results of the present study revealed that LIMD2 promoted NSCLC progression and was regulated by miRâ34a.
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