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Arraystar inc human mirna expression microarray v4.0
Curcumol upregulates miR-7 expression in GC cells. a, <t>miRNAs</t> with differential expression in cells after curcumol treatment identified by <t>microarray</t> analysis; b, miR-7 expression in cells after 80 μM curcumol treatment examined by RT-qPCR (* p < 0.05; two-way ANOVA); c, miR-7 expression in tumor and the paired normal tissues evaluated by RT-qPCR (n = 33; * p < 0.05; the unpaired t test); d, correlation between miR-7 expression and the patient’s survival (* p < 0.05; Kaplan-Meier analysis); e, miR-7 expression in MKN45 and HGC27 cells after different doses of curcumol treatment examined by RT-qPCR (* p < 0.05, ** p < 0.01; two-way ANOVA).
Human Mirna Expression Microarray V4.0, supplied by Arraystar inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Article Title: Curcumol enhances cisplatin sensitivity of gastric cancer: involvement of microRNA-7 and the nuclear factor-kappa B/snail family transcriptional repressor 1 axis

Journal: Bioengineered

doi: 10.1080/21655979.2022.2070975

Curcumol upregulates miR-7 expression in GC cells. a, miRNAs with differential expression in cells after curcumol treatment identified by microarray analysis; b, miR-7 expression in cells after 80 μM curcumol treatment examined by RT-qPCR (* p < 0.05; two-way ANOVA); c, miR-7 expression in tumor and the paired normal tissues evaluated by RT-qPCR (n = 33; * p < 0.05; the unpaired t test); d, correlation between miR-7 expression and the patient’s survival (* p < 0.05; Kaplan-Meier analysis); e, miR-7 expression in MKN45 and HGC27 cells after different doses of curcumol treatment examined by RT-qPCR (* p < 0.05, ** p < 0.01; two-way ANOVA).
Figure Legend Snippet: Curcumol upregulates miR-7 expression in GC cells. a, miRNAs with differential expression in cells after curcumol treatment identified by microarray analysis; b, miR-7 expression in cells after 80 μM curcumol treatment examined by RT-qPCR (* p < 0.05; two-way ANOVA); c, miR-7 expression in tumor and the paired normal tissues evaluated by RT-qPCR (n = 33; * p < 0.05; the unpaired t test); d, correlation between miR-7 expression and the patient’s survival (* p < 0.05; Kaplan-Meier analysis); e, miR-7 expression in MKN45 and HGC27 cells after different doses of curcumol treatment examined by RT-qPCR (* p < 0.05, ** p < 0.01; two-way ANOVA).

Techniques Used: Expressing, Quantitative Proteomics, Microarray, Quantitative RT-PCR

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other:

Article Title: Curcumol enhances cisplatin sensitivity of gastric cancer: involvement of microRNA-7 and the nuclear factor-kappa B/snail family transcriptional repressor 1 axis.
Article Snippet: This reaction was performed at 37°C for 30 min. After that, the labeled RNA was hybridized with Human miRNA Expression Microarray V4.0 (Arraystar, Rockville, MD, USA) for 24 h. The gene expression data were obtained using a GeneChipTM Scanner 3000 7 G system (#00-0210, 2008, Thermo Fisher Scientific) and analyzed by the R Language Program (Version 3.6.3, R).

Article Title: Breast Cancer Stem Cells-derived Extracellular Vesicles Affect PPARG Expression by Delivering MicroRNA-197 in Breast Cancer Cells.
Article Snippet: 1, Breast cancer (BC) is the most frequently diagnosed cancer in women which is often associated with metastasis; 2, We found that BC stem cells-derived extracellular vesicles promote metastasis of BC cells by elevating microRNA-197; 3, microRNA-197 induces epithelial-mesenchymal transition in BC by targeting PPARG; 4, This study offers a possible target for the treatment of liver metastases in BC.. Background: Breast cancer (BC) is the most frequently diagnosed cancer in women, and over 90% of BC-related deaths are associated with metastasis.. The effects of BC stem cells-derived extracellular vesicles (BCSCs-EVs) have been implicated in cancer control.

Article Title: Curcumol enhances cisplatin sensitivity of gastric cancer: involvement of microRNA-7 and the nuclear factor-kappa B/snail family transcriptional repressor 1 axis
Article Snippet: This reaction was performed at 37°C for 30 min. After that, the labeled RNA was hybridized with Human miRNA Expression Microarray V4.0 (Arraystar, Rockville, MD, USA) for 24 h. The gene expression data were obtained using a GeneChip TM Scanner 3000 7 G system (#00-0210, 2008, Thermo Fisher Scientific) and analyzed by the R Language Program (Version 3.6.3, R).

Article Title: Sevoflurane attenuates cardiomyocyte apoptosis by mediating the miR-219a/AIM2/TLR4/MyD88 axis in myocardial ischemia/reperfusion injury in mice.
Article Snippet: Next, 0.5 μg RNA was used for hybridization using Human miRNA Expression Array V4.0 (Arraystar Inc., Rockville, MD, USA).

Article Title: Histone deacetylase HDAC2 regulates microRNA‐125a expression in neuroblastoma
Article Snippet: The cDNA was then hybridized with Human miRNA Expression Microarray V4.0 (Arraystar Inc., Rockville, MD, USA) and GeneChip Human Gene 1.0 ST Array (Thermo Fisher Scientific).

Expressing:

Article Title: MiR-223-3p regulates erythropoiesis by targeting TGFBR3/Smad signaling pathway in hemoglobin H-Constant Spring disease.
Article Snippet: .. ArrayStar Human miRNA Array and ArrayStar Human mRNA Array were used to analyze the expression of miRNAs and mRNAs. ..

Article Title: Inhibition of MicroRNA-302c on Stemness of Colon Cancer Stem Cells via the CARF/Wnt/β-Catenin Axis.
Article Snippet: Background Even though the relevance of microRNA (miR)-302c has been studied, little is known about its involvement in colon cancer (CC).. Aims Our aim here was to investigate the role of miR-302c in the cancer stem cells (CSCs) of CC.. Methods Firstly, the CSCs were screened out from cultured SW1116 and SW480 cells by flow cytometry, and the differentially expressed miRNAs in cell were obtained by microarray analysis.



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