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miRBase |
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![]() 4 publications mentioning hsa-mir-1245aOpen access articles that are associated with the species Homo sapiens and mention the gene name mir-1245a. Click the [+] symbols to view sentences that include the gene name, or the word cloud on the right for a summary. |
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Other miRNAs from this paper: mmu-mir-134, hsa-mir-7-1, hsa-mir-7-2, hsa-mir-7-3, hsa-mir-214, hsa-mir-134, mmu-mir-214, mmu-mir-7a-1, mmu-mir-7a-2, mmu-mir-7b, hsa-mir-1252, hsa-mir-1245b
The results showed that the overexpression of circ_0046264 or the suppression of miR-1245 promoted the expression of BRCA2, whereas the suppression of circ_0046264 led to the suppression of BRCA2 expression (Fig. 2g, j, 3a).
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[#] P < 0.05, compared with circ264 group Overexpression of hsa_circ_0046264 or suppression of miR-1245 significantly suppressed the invasion and viability of lung cancer cells; and the suppression of hsa_circ_0046264 or the overexpression of miR-1245 significantly suppressed cell invasion and viability (Fig. 3b, 4a and b).
[score:12]
Here, hsa_circ_0046264 and BRCA2 shared common target miRNA, miR-1245, and up-regulation of miR-1245 in lung cancer resulted from the low expression of hsa_circ_0046264 caused the down-regulation of BRCA2.
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The suppressive effect of hsa_circ_0046264 resulted from its combination with miR-1245, which could indirectly up-regulate miR-1245’s target gene, BRCA2.
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Overexpression of hsa_circ_0046264 could up-regulate BRCA2 expression through down -regulating of miR-1245.
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Fig. 2Hsa_circ_0046264 overexpression down-regulated miR-1245 and up-regulated BRCA2.
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Hsa_circ_0046264 overexpression down-regulated miR-1245 and up-regulated BRCA2.
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MiR-1245 was suppressed by hsa_circ_0046264, while BRCA2, the target gene of miR-1245, was up-regulated.
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Hsa_circ_0046264 induced apoptosis but inhibited proliferation and invasion of lung cancer cells through targeting miR-1245 to up-regulate BRCA2.
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Hsa_circ_0046264 could bind miR-1245, and since BRCA2 was the target gene of miR-1245, BRCA2 was indirectly up-regulated by hsa_circ_0046264.
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a The overexpression of hsa_circ_0046264 and the suppression of miR-1245 promoted BRCA2 expression.
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Meanwhile, miR-1245 expression was reduced in tumor tissues obtained from mice in hsa_circ_0046264 overexpression group, and the mRNA and protein expressions of BRCA2 were elevated.
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Hsa_circ_0046264 and BRCA2 were down-regulated in lung cancer tissues while miR-1245 was up-regulated.
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Hsa_circ_0046264 inhibited lung cancer development through acting as a ceRNA which regulated miR-1245 and indirectly activated BRCA2.
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The deletion mutation (MUT1) and point mutation (MUT2) of circ_0046264 and BRCA2 were used to be as the control of wild type vectors (WT) which showed significant suppressions of luciferase activity by miR-1245(Fig. 2c and d).
[score:5]
b The overexpression of hsa_circ_0046264 and the suppression of miR-1245 promoted cell invasion.
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The tumor tissues obtained from the nude mice had an elevated expression level of hsa_circ_0046264 in circ264 group, accompanied by lower miR-1245 and higher BRCA2 expression levels (Fig. 5c and d).
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Hsa_circ_0046264 and BRCA2 were lowly expressed in lung cancer tissues while miR-1245 was high expressed.
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The regulatory effect of miR-1245on BRCA2 expression has been reported in previous study as the 3’UTR region of BRCA2 was combined with miR-1245 [15].
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The target gene of miR-1245 was determined as BRCA2 through the database miRTarBass.
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c- d Apoptosis of A549 and 95-D cells was promoted in circ264 group and antimir1245 group but inhibited in sicirc groups and mir1245 group.
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The overexpression of miR-1245 significantly enhanced cell apoptosis as well (Fig. 4c and d).
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a The expression level of miR-1245 was higher in advanced lung cancer tissues (stage III and stage IV) than that in early-stage cancer tissues (stage I and stage II).
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We have verified the target relationship between circ_0046264 and miR-1245 as well as miR-1245 and BRCA2.
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f, i The relative expression of miR-1245 in lung cancer cells decreased in circ264 group and antimir1245 group but increased in sicirc groups and miR-1245 group.
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In addition, the influence of modulation of circ_0046264 and miR-1245 expression on BRCA expression was investigated.
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We confirmed the target relationship between miR-1245 and BRCA2, and further uncovered their associations with hsa_circ_0046264.
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Therefore, miR-1245 and its target gene BRCA2 might affect the progression of lung cancers.
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These results implied that miR-1245 is a potential tumor promotor and BRCA2 is a suppressor.
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The concentration of miR-1245 mimics or miR-1245 inhibitor was 30 nM–50 nM.
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d The relative expression of miR-1245 decreased while that of BRCA2 increased in tumor tissues of circ264 group.
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The simultaneous transfection of hsa_circ_0046264 and miR-1245 did not result in significant change of BRCA2 expression.
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MiR-1245 was considered as an oncogene because it was demonstrated as a potent negative regulator of the tumor suppressor protein BRCA2 [13].
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MiR-1245 attenuated the expression of NKG2D, an activating receptor involved in tumor immunosurveillance, in natural killer cells [14].
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HEK293 cells (Thermo Fisher Scientific) transfected with miR-1245 mimics or miR-con were seeded in 24-well plates and co -transfected with empty pmirGLO or recombinant pmirGLO for 48 h by using Lipofectamine™ 2000 (Invitrogen).
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The influence of miR-1245 in lung cancer has not been identified yet.
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d The dual luciferase activity decreased in HEK293 cells co -transfected with BRCA2 3’UTR WT and miR-1245 mimics, but almost not changed in cells co -transfected with BRCA2 3’UTR MUT and miR-1245 mimics.
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c The dual luciferase activity decreased in HEK293 cells co -transfected with hsa_circ_0046264 WT and miR-1245 mimics, but almost did not change in cells co -transfected with hsa_circ_0046264 MUT and miR-1245 mimics.
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The simultaneous transfection of hsa_circ_0046264 and miR-1245 did not result in significant change of cell invasion.
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The transfection efficiency of circ264, sicirc, miR-1245 and antimiR-1245 were tested in both A549 and 95-D cell lines (Fig. 2e and f, h and i).
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hsa_circ_0046264 Hsa-miR-1245 BRCA2 Lung cancer Lung cancer mortality ranks the highest in cancer-related death, and the five-year survival rate is only about 20% [1].
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Other miRNAs from this paper: hsa-mir-15a, hsa-mir-16-1, hsa-mir-17, hsa-mir-19a, hsa-mir-21, hsa-mir-32, hsa-mir-33a, hsa-mir-101-1, hsa-mir-29b-1, hsa-mir-29b-2, hsa-mir-215, hsa-mir-141, hsa-mir-142, hsa-mir-146a, hsa-mir-193a, hsa-mir-155, hsa-mir-29c, hsa-mir-101-2, hsa-mir-494, hsa-mir-765, hsa-mir-1248, hsa-mir-1275, hsa-mir-1973, hsa-mir-1245b
Our results demonstrate that a) two miRNAs, miR-193a-3p and miRPlus-E1245 (a proprietary sequence of Exiqon Inc, Denmark and named as such to differentiate from miR-1245) were commonly regulated among all 4 cell types infected with XMRV used in the study, and b) while miR-193a-3p is down regulated, miRPlus-E1245 exhibited varied expression profile in the four cell types infected with XMRV.
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The miRPlus-E1245 is a recently discovered miRNA and proprietary sequence of Exiqon Inc, Denmark and named as such to differentiate it from miR-1245.
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Other miRNAs from this paper: hsa-let-7a-1, hsa-let-7a-2, hsa-let-7a-3, hsa-let-7b, hsa-let-7c, hsa-let-7d, hsa-let-7e, hsa-let-7f-1, hsa-let-7f-2, hsa-mir-18a, hsa-mir-30d, hsa-mir-182, hsa-mir-200b, hsa-let-7g, hsa-let-7i, hsa-mir-138-2, hsa-mir-134, hsa-mir-138-1, hsa-mir-200c, hsa-mir-155, hsa-mir-200a, hsa-mir-302a, hsa-mir-302b, hsa-mir-302c, hsa-mir-302d, hsa-mir-367, hsa-mir-369, hsa-mir-373, hsa-mir-328, hsa-mir-491, hsa-mir-515-1, hsa-mir-515-2, hsa-mir-607, hsa-mir-1260a, hsa-mir-302e, hsa-mir-302f, hsa-mir-1260b, hsa-mir-3919, hsa-mir-1245b
Name Predicted targets (miRDB) 1 miR-200b ZEB1, ZEB2, BMI1, TWISTNB, PLEXINA4, DNMT3A, CDNK2B 2 miR-607 RUNX-1, RUNX-2, IGF-1, MSX1, SOCS4, CXCL6 3 miR-515-5p FGFR2, TGFBR2, NOTCH2, BMP8b, MSX2, FGF12, BMPR1B 4 miR-1245 FGF20, TBRG1, BMI1 5 miR-3919 NFAT5, ID4, HOXB13, HDAC1, RPS6KA6, TGFBR2, SEMA3A 6 miR-182 FGF9, SMAD1, IGF1R, SOX2, BMPR1B, WISP1/CCN4, EGR3 Table shows the selected possible mRNA targets related to stemness and cell differentiation.
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The levels of other lymphocyte-expressed miRNAs such as miR-1245 [31] and miR-223 [32] were not significantly affected by resveratrol treatment.
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