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Low expression of miR-192 in NSCLC and its tumor suppressor functions in metastasis via targeting ZEB2

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AbstractObjectivesLung cancer is the leading cause of cancer-related death, with non-small cell lung cancer (NSCLC) accounting for more than 80% of all lung cancer cases. The aim of this study was to investigate the function and underlying mechanism of microRNA-192 (miR-192) in metastasis of NSCLC cells.MethodsReal-time PCR was applied to quantify the expression of miR-192 in NSCLC tissues and cell lines, matched with their corresponding controls. The biological roles of miR-192 were studied in NSCLC cells using the wound healing and trans well invasion assays. Real-time PCR and western blot were used to evaluate the regulation of ZEB2 by miR- 192.ResultsMiR-192 was expressed significantly lower in NSCLC tissues/cells when compared with controls. Ectopic expression of miR-192 strongly inhibited cell migration and invasion in NSCLC A549 cells. Further investigation revealed ZEB2, an EMT regulator, was one of the downstream targets regulated by miR-192.ConclusionThese results suggested that miR-192 inhibits the metastasis of NSCLC cells by targeting ZEB2, and thus is an important tumor suppressor.
Title: Low expression of miR-192 in NSCLC and its tumor suppressor functions in metastasis via targeting ZEB2
Description:
AbstractObjectivesLung cancer is the leading cause of cancer-related death, with non-small cell lung cancer (NSCLC) accounting for more than 80% of all lung cancer cases.
The aim of this study was to investigate the function and underlying mechanism of microRNA-192 (miR-192) in metastasis of NSCLC cells.
MethodsReal-time PCR was applied to quantify the expression of miR-192 in NSCLC tissues and cell lines, matched with their corresponding controls.
The biological roles of miR-192 were studied in NSCLC cells using the wound healing and trans well invasion assays.
Real-time PCR and western blot were used to evaluate the regulation of ZEB2 by miR- 192.
ResultsMiR-192 was expressed significantly lower in NSCLC tissues/cells when compared with controls.
Ectopic expression of miR-192 strongly inhibited cell migration and invasion in NSCLC A549 cells.
Further investigation revealed ZEB2, an EMT regulator, was one of the downstream targets regulated by miR-192.
ConclusionThese results suggested that miR-192 inhibits the metastasis of NSCLC cells by targeting ZEB2, and thus is an important tumor suppressor.

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