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miRBase |
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![]() 12 publications mentioning hsa-mir-1202Open access articles that are associated with the species Homo sapiens and mention the gene name mir-1202. 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: hsa-mir-31, hsa-mir-100, hsa-mir-199a-1, hsa-mir-199a-2, hsa-mir-204, hsa-mir-205, hsa-mir-210, hsa-mir-214, hsa-mir-223, hsa-mir-200b, hsa-mir-9-1, hsa-mir-9-2, hsa-mir-9-3, hsa-mir-146a, hsa-mir-206, hsa-mir-200c, hsa-mir-200a, hsa-mir-340, hsa-mir-516a-1, hsa-mir-516a-2, hsa-mir-455, hsa-mir-1181
We found 37 differentially expressed miRNAs in the CD133 [+] spheroid-forming subpopulation of OVCAR3 cells, 34 of which were significantly up-regulated, including miR-205, miR-146a, miR-200a, miR-200b, and miR-3, and 3 of which were significantly down-regulated, including miR-1202 and miR-1181.
[score:9]
Thirty-four miRNAs including miR-205, miR-146a, miR-200a, miR-200b, and miR-31 were significantly up-regulated, while 3 microRNAs including miR-1202 and miR-1181 were significantly down-regulated (Figure 5, Table 1).
[score:7]
In agreement with the microarray results, miR-205, miR-146a, miR-200a, miR-200b, and miR-31 were up-regulated, whereas miR-1202 and miR-1181 were down-regulated in the CD133 [+] spheroid-forming subpopulation (Table 2).
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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-let-7g, hsa-let-7i, hsa-mir-143, hsa-mir-515-1, hsa-mir-515-2, hsa-mir-603, hsa-mir-891a, hsa-mir-892a, hsa-mir-890, hsa-mir-891b, hsa-mir-888, hsa-mir-892b, hsa-mir-1908
lncRNA Alternative splicing [37] Neuro development [39] lincHPAT Embryo development [40] FMR4 Antiapoptotic [43] Psoriasis disease [44]
miRNA C19MC Preeclampsia; cancers [68] X-linked miRNA cluster Possible roles in epididymal physiology; sperm maturity; male fertility; tube development [73], [74] miR-1202 Major depressive disorder [79] miR-1908-5p Bipolar disorder [80] miR-603 Pre-miR-603 with rs11014002 SNP having protective effect toward Alzheimer’s disease [83], [84]
Despite the great advances, there are some limitations that need to be overcome for future studies.
[score:8]
Notably, higher GRM4 protein expression is also detected in postmortem brain samples and clinical samples from patients with depression, suggesting negative correlation with the expression of miR-1202 [79].
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These studies suggest that miR-1202 could be a potential target for new antidepressant treatment as well as biomarker for treatment prediction and response [79].
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The primate-specific miR-1202 has recently been shown to target GRM4 [79].
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miR-1202 is further validated experimentally to have higher expression in humans as compared to non-human primates [79].
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In silico sequence comparison among 100 animal genomes shows that miR-1202 is present only in primates.
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Other miRNAs from this paper: hsa-let-7e, hsa-mir-21, hsa-mir-23a, hsa-mir-24-1, hsa-mir-24-2, hsa-mir-30a, hsa-mir-31, hsa-mir-183, hsa-mir-203a, hsa-mir-205, hsa-mir-210, hsa-mir-221, hsa-mir-222, hsa-mir-23b, hsa-mir-125b-1, hsa-mir-130a, hsa-mir-125b-2, hsa-mir-193b, hsa-mir-545, hsa-mir-660, hsa-mir-421, hsa-mir-762, hsa-mir-4291, hsa-mir-23c, hsa-mir-203b
The other four differentially expressed miRNAs (miRNA-762, miRNA-1202, miRNA-4291 and miRNA-30a*) were not found to have the target genes anticorrelated with their expressions, indicating that they regulated the expression of target genes possibly by translational inhibition.
[score:16]
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Other miRNAs from this paper: hsa-mir-204, hsa-mir-224, hsa-mir-383, hsa-mir-610, hsa-mir-637, hsa-mir-659, hsa-mir-1266
We observed differing expression of miR-224 and miR-383, whereas expression of the five other candidate miRNAs: miR-610, miR-637, miR-659, miR-1202 and miR-1266 did not differ significantly between ccRCC and control tissue (Figure S1, Supplemental Data).
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We identified 7 potential miRNAs targeting the 3′UTR of human DIO1 (Table 1): miR-224, miR-383, miR-610, miR-659, miR-637, miR-1202 and miR-1266.
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Expression of miR-224, miR-383, miR-610, miR-637, miR-659, miR-1202 and miR-1266 was analyzed in 32 matched pairs of tumor (T) and control (C) samples.
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Other miRNAs from this paper: hsa-mir-199a-1, hsa-mir-139, hsa-mir-183, hsa-mir-199a-2, hsa-mir-125b-1, hsa-mir-125b-2, hsa-mir-150, hsa-mir-328, hsa-mir-483, hsa-mir-494, hsa-mir-572, hsa-mir-574, hsa-mir-638, hsa-mir-762, hsa-mir-885, hsa-mir-940, hsa-mir-1225, hsa-mir-1238, hsa-mir-1207, hsa-mir-1275, hsa-mir-1915, hsa-mir-1973, hsa-mir-3162, hsa-mir-3196, hsa-mir-4299, hsa-mir-4284, hsa-mir-3679, hsa-mir-3940, hsa-mir-4485, hsa-mir-4516, hsa-mir-4530, hsa-mir-4649, hsa-mir-4728, hsa-mir-4739, hsa-mir-371b, hsa-mir-4787, hsa-mir-5787, hsa-mir-6069, hsa-mir-6090
Nineteen of the downregulated miRNAs in chronic patients were found to be associated with carcinogenesis in various organs and tissues, such as miR-1207 [40], miR-3162-5p [41, 42], miR-3196 [43, 44], miR-371b-5p [45], miR-574-5p [46, 47], miR-1225-5p [48], miR-4485 [49], miR-572 [50], miR-4299 [51], miR-3679-5p [52], miR-3940-5p [53], miR-638 [54, 55], miR-1202 [56], miR-5787 [57], miR-1973 [58], miR-4532 [59], miR-1275 [60], miR-4728-5p [61], and miR-1915-3p [62].
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Other miRNAs from this paper: hsa-mir-15a, hsa-mir-17, hsa-mir-106a, hsa-mir-30b, hsa-mir-302d, hsa-mir-612, hsa-mir-661, hsa-mir-660, hsa-mir-1184-1, hsa-mir-1285-1, hsa-mir-1285-2, hsa-mir-1304, hsa-mir-1184-2, hsa-mir-1184-3, hsa-mir-3689b, hsa-mir-3689c, hsa-mir-4647, hsa-mir-4739, hsa-mir-7156
Interestingly, many of the genes containing such highly differentiated SNPs in the Alu-miRNA sites within their 3′UTRs (listed in Table 1) have target sites (encompassing these SNPs) for miRNAs that are primate-specific (miR-661 29, miR-1202 53), human-specific (miR-4739, miR-5095) 54, involved in the regulation of p53 signaling (miR-660 55, miR-661 29, miR-1285 56) or in the apoptosis pathway (miR-17 44 45, miR-30b 57, miR-106a-3p 45, miR-612 58).
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Other miRNAs from this paper: hsa-mir-149, hsa-mir-572, hsa-mir-663a, hsa-mir-762, hsa-mir-1225, hsa-mir-371b, hsa-mir-4763, hsa-mir-5001, hsa-mir-5787, hsa-mir-6791
Among the top ten fold changed miRNAs (Supplementary Table 1), half of them (hsa-miR-371b-5p, hsa-miR-663a, hsa-miR-1225-5p, hsa-miR-1202, and hsa-miR-572) were closely linked to the occurrence and development of tumors and might play vital roles as oncogenes or tumor suppressor genes [28– 31].
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Other miRNAs from this paper: hsa-let-7a-1, hsa-let-7a-2, hsa-let-7a-3, hsa-mir-16-1, hsa-mir-21, hsa-mir-29a, hsa-mir-16-2, hsa-mir-320a, hsa-mir-638, hsa-mir-320b-1, hsa-mir-320c-1, hsa-mir-320b-2, hsa-mir-1225, hsa-mir-1207, hsa-mir-320d-1, hsa-mir-320c-2, hsa-mir-320d-2, hsa-mir-320e
Using a step-wise approach, we selected five exosomal miRNAs (miR-320c, miR-1202, miR-1225-5p, miR-1207-5p, and miR-7270) and validated miR-320 and miR1225-5p expression in the PLF of 18 CG patients by qRT-PCR.
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Other miRNAs from this paper: hsa-let-7f-1, hsa-let-7f-2, hsa-mir-15a, hsa-mir-16-1, hsa-mir-17, hsa-mir-22, hsa-mir-25, hsa-mir-27a, hsa-mir-29a, hsa-mir-92a-1, hsa-mir-92a-2, hsa-mir-29b-1, hsa-mir-16-2, hsa-mir-199a-1, hsa-mir-34a, hsa-mir-199a-2, hsa-let-7i, hsa-mir-15b, hsa-mir-132, hsa-mir-106b, hsa-mir-130b, hsa-mir-365a, hsa-mir-324, hsa-mir-196b, hsa-mir-429, hsa-mir-494, hsa-mir-193b, hsa-mir-572, hsa-mir-638, hsa-mir-320b-1, hsa-mir-320c-1, hsa-mir-320b-2, hsa-mir-1305, hsa-mir-1260a, hsa-mir-320d-1, hsa-mir-320c-2, hsa-mir-320d-2, hsa-mir-1915
In contrast, for the second set of MSCs, 6 out of the 11 miRNAs (miR-196b-5p, miR-16-5p, miR-1202, miR-572, miR-638, and miR-15b-5p) evaluated for cellular aging were statistically significant (p < 0.05) between passage 4 and 8. miRNAs, miR-572 and miR-638 were significant in the second set of MSCs and upregulated at the later passage by 1.59 and 1.35, respectively.
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Other miRNAs from this paper: hsa-let-7a-1, hsa-let-7a-2, hsa-let-7a-3, hsa-let-7c, hsa-mir-21, hsa-mir-98, hsa-mir-10a, hsa-mir-182, hsa-mir-221, hsa-mir-222, hsa-mir-185, hsa-mir-320a, hsa-mir-372, hsa-mir-373, hsa-mir-382, hsa-mir-151a, hsa-mir-491, hsa-mir-590, hsa-mir-151b
miR-1202 is a primate-specific and brain-enriched microRNA involved in major depression and antidepressant treatment.
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This little known gene resides in the short intergenic region between NOX3 and MIR1202.
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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-let-7g, hsa-let-7i, hsa-mir-125b-1, hsa-mir-128-1, hsa-mir-125a, hsa-mir-125b-2, hsa-mir-128-2, hsa-mir-451a, hsa-mir-574, hsa-mir-593, hsa-mir-595, hsa-mir-603, hsa-mir-647, hsa-mir-663a, hsa-mir-671, hsa-mir-921, hsa-mir-297, hsa-mir-1183, hsa-mir-663b, hsa-mir-1207, hsa-mir-1299, hsa-mir-1275, hsa-mir-664a, hsa-mir-451b, hsa-mir-664b
miR-1202 is a primate-specific and brain-enriched microRNA involved in major depression and antidepressant treatment.
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