2020
DOI: 10.5114/aoms.2019.87761
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MiR-135b-5p promotes viability, proliferation, migration and invasion of gastric cancer cells by targeting Krüppel-like factor 4 (KLF4)

Abstract: Introduction: The expression of MiR-135b-5p was up-regulated while Krüppel-like factor 4 (KLF4) expression was extremely low in human gastric carcinoma (GC) tissues. This study aimed to explore the role of miR-135b-5p in GC cells and its influence on various cell capacity and viability by targeting KLF4. Material and methods: The dual-luciferase reporter assay was first performed and the target relationship between miR-135b-5p and KLF4 was confirmed. Then three GC cell lines and the human normal gastric epithe… Show more

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Cited by 39 publications
(26 citation statements)
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“…Cox regression analysis in patients with non-small cell lung cancer. Numerous studies have indicated that miRNAs are involved in the pathogenesis of human cancer by regulating tumor cell processes, such as proliferation, migration and invasion (30)(31)(32). Therefore, the present study carried out further cellular experiments to uncover the functional role of miR-665 in NSCLC progression.…”
Section: Discussionmentioning
confidence: 91%
“…Cox regression analysis in patients with non-small cell lung cancer. Numerous studies have indicated that miRNAs are involved in the pathogenesis of human cancer by regulating tumor cell processes, such as proliferation, migration and invasion (30)(31)(32). Therefore, the present study carried out further cellular experiments to uncover the functional role of miR-665 in NSCLC progression.…”
Section: Discussionmentioning
confidence: 91%
“…Indeed, our results suggest that many aberrantly expressed circRNAs regulated many genes function in cancer-related pathways ( Figures S3–S5 ). miR-135b-5p is also reported to target KLF4 [ 67 ], an important transcription factor in skin barrier formation [ 68 ]; a pathway that is disrupted in psoriasis.…”
Section: Discussionmentioning
confidence: 99%
“…A previous study has shown that overexpression of KLF4 will lead to a decrease in the expression of N-cadherin, MMP2, and MMP9 [ 34 ]. On the contrary, the loss of KLF4 weakened the inhibition of N-cadherin, MMP2, and MMP9, leading to increased tumor cell invasion and migration, thereby affecting survival and prognosis [ 35 ]. KLF5, in contrast to KLF4, showed high expression in gastrointestinal tumors.…”
Section: Discussionmentioning
confidence: 99%