MIR622, microRNA 622, 693207

N. diseases: 48; N. variants: 0
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0027651
Disease: Neoplasms
Neoplasms
0.100 AlteredExpression group BEFREE We found that overexpression of miR-622 inhibited CRC angiogenesis in vitro, according to suppression of proliferation, migration, tube formation, and invasiveness of human umbilical vein endothelial cells (HUVECs) treated with a tumor cell-conditioned medium derived from Caco-2 or HT-29 cells. 30851425 2019
CUI: C0027651
Disease: Neoplasms
Neoplasms
0.100 Biomarker group BEFREE It has recently been shown that miR-622 plays a tumor suppressive role in many human cancers. 28796324 2018
CUI: C0027651
Disease: Neoplasms
Neoplasms
0.100 Biomarker group BEFREE MiR-622 plays as a tumor inhibitor in some types of cancer, however, its role in kidney cancer is unknown. 29507713 2018
CUI: C0027651
Disease: Neoplasms
Neoplasms
0.100 Biomarker group BEFREE These results show that miR-622 acts as a tumor suppressor in thyroid cancer, at least in part, via targeting VEGFA, and suggest that miR-622 may serves as a potential target for treatment of thyroid cancer patients. 29593418 2018
CUI: C0027651
Disease: Neoplasms
Neoplasms
0.100 Biomarker group BEFREE We conclude that miR-622 is a novel tumor suppressor in melanoma and identify the miR-622-KRAS axis as potential therapeutic target. 29495114 2018
CUI: C0027651
Disease: Neoplasms
Neoplasms
0.100 AlteredExpression group BEFREE We applied quantitative polymerase chain reaction to determine the levels of miR-139-3p and miR-622 in 42 pairs of tumor and adjacent non-tumor tissues, and in serum samples of 117 patients and 90 control subjects. 28404964 2017
CUI: C0027651
Disease: Neoplasms
Neoplasms
0.100 Biomarker group BEFREE Furthermore, we confirmed that miR-622 inhibited tumor proliferation and migration in vitro. 26333174 2016
CUI: C0027651
Disease: Neoplasms
Neoplasms
0.100 Biomarker group BEFREE These findings indicate that miR-622 may act as a tumor suppressor in ESCC and would serve as a potential therapy target for this disease. 27501502 2016
CUI: C0027651
Disease: Neoplasms
Neoplasms
0.100 AlteredExpression group BEFREE Overexpression of miR-622 suppressed tumor cell proliferation, migration, and invasion of A172, U87, and U251 cells. 26596833 2016
CUI: C0027651
Disease: Neoplasms
Neoplasms
0.100 AlteredExpression group BEFREE Ectopic expression of miR-622 led to a significant reduction of MAP4K4 expression in HCC cells and xenograft tumors. 26467022 2015
CUI: C0027651
Disease: Neoplasms
Neoplasms
0.100 Biomarker group BEFREE In summary, miR-622 functions as a tumor suppressor by targeting K-Ras and impacting the anticancer effect of resveratrol. 22016468 2012
CUI: C0027651
Disease: Neoplasms
Neoplasms
0.100 Biomarker group BEFREE More importantly, Lynch syndrome tumors displayed a unique miRNA profile compared with sporadic MSI tumors; miR-622, miR-1238, and miR-192 were the most differentially expressed miRNAs between these two groups. 21844009 2011
CUI: C1269955
Disease: Tumor Cell Invasion
Tumor Cell Invasion
0.090 AlteredExpression phenotype BEFREE A novel circular RNA, hsa-circ-0000211, promotes lung adenocarcinoma migration and invasion through sponging of hsa-miR-622 and modulating HIF1-α expression. 31668923 2020
CUI: C1269955
Disease: Tumor Cell Invasion
Tumor Cell Invasion
0.090 Biomarker phenotype BEFREE Previous studies have shown that microRNA-622 (miR-622) was associated with glioma proliferation and invasion. 31686846 2019
CUI: C1269955
Disease: Tumor Cell Invasion
Tumor Cell Invasion
0.090 AlteredExpression phenotype BEFREE The overexpression of miR-622 in TPC-1 cells inhibited cell proliferation, migration and invasion in vitro, as well as suppress tumor growth in vivo. 29593418 2018
CUI: C1269955
Disease: Tumor Cell Invasion
Tumor Cell Invasion
0.090 Biomarker phenotype BEFREE An antisense experiment was executed to further confirm the role miR-622 had played with regard to migration and invasion by targeting regulation of DYRK2 pathway in CRC cells. 28260923 2017
CUI: C1269955
Disease: Tumor Cell Invasion
Tumor Cell Invasion
0.090 Biomarker phenotype BEFREE Moreover, we found overexpression of c-Myc can strengthen the effects of miR-622 on the proliferation, migration and invasion of CCA cells. 28961507 2017
CUI: C1269955
Disease: Tumor Cell Invasion
Tumor Cell Invasion
0.090 AlteredExpression phenotype BEFREE Up-regulation of miR-622 could significantly reduce ESCC cell proliferation, enhance cell apoptosis, and impair cell invasion and migration in vitro, while down-regulation of miR-622 showed opposite effects. 27501502 2016
CUI: C1269955
Disease: Tumor Cell Invasion
Tumor Cell Invasion
0.090 Biomarker phenotype BEFREE Our findings provide insight into the specific biological behavior of miR-622 in tumor invasion and migration. 25258251 2015
CUI: C1269955
Disease: Tumor Cell Invasion
Tumor Cell Invasion
0.090 Biomarker phenotype BEFREE Functional analyses revealed that increased miR-622 expression inhibited lung cancer cell migration and invasion in vitro. miR-622 also inhibited the genesis of metastatic lung nodules as demonstrated in a lung cancer xenograft model in which nude mice were transplanted with A549 cells expressing miR-622. 26528854 2015
CUI: C1269955
Disease: Tumor Cell Invasion
Tumor Cell Invasion
0.090 AlteredExpression phenotype BEFREE Down-regulation of miR-622 in gastric cancer promotes cellular invasion and tumor metastasis by targeting ING1 gene. 21528065 2011
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.050 Biomarker disease BEFREE Taken together, these data show that miR-622 inhibits CRC angiogenesis by suppressing the CXCR4-VEGFA signaling axis, which represents a promising target for developing a new therapeutic strategy against CRC. 30851425 2019
CUI: C0027627
Disease: Neoplasm Metastasis
Neoplasm Metastasis
0.050 Biomarker phenotype BEFREE Our previous study has revealed that miR-622 inhibits colorectal cancer (CRC) metastasis. 30851425 2019
CUI: C0027627
Disease: Neoplasm Metastasis
Neoplasm Metastasis
0.050 Biomarker phenotype BEFREE Thus, with previous experimental evidences, the present review discussed the role of FoxOs in association with metastasis related molecules including cannabinoid receptor 1 (CNR1), Cdc25A/Cdk2, Src, serum and glucocorticoid inducible kinases (SGKs), CXCR4, E-cadherin, annexin A8 (ANXA8), Zinc finger E-box-binding homeobox 2 (ZEB2), human epidermal growth factor receptor 2 (HER2) and mRNAs such as miR-182, miR-135b, miR-499-5p, miR-1274a, miR-150, miR-34b/c and miR-622, subsequently analyzed the molecular mechanism of some natural compounds targeting FoxOs and finally suggested future research directions in cancer progression and metastasis. 28774834 2018
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.050 Biomarker disease BEFREE The function of microRNA-622 (miR-622) in colorectal cancer (CRC) remains controversial. 28260923 2017