m6A Target Gene Information
General Information of the m6A Target Gene (ID: M6ATAR00379)
Full List of m6A Methylation Regulator of This Target Gene and Corresponding Disease/Drug Response(s)
KRAS
can be regulated by the following regulator(s), and cause disease/drug response(s). You can browse detail information of regulator(s) or disease/drug response(s).
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Heterogeneous nuclear ribonucleoproteins A2/B1 (HNRNPA2B1) [READER]
In total 1 item(s) under this regulator | ||||
Experiment 1 Reporting the m6A Methylation Regulator of This Target Gene | [1] | |||
Response Summary | UCA1 increases GTPase KRas (KRAS) phosphorylation by interacting with hnRNPA2B1 and that UCA1 functions as a molecular sponge for miR-590-3p to promote KRAS expression. the UCA1-KRAS axis plays a crucial role in pancreatic ductal adenocarcinoma progression and that UCA1 serves as a target for new PDAC therapies. | |||
Target Regulation | Up regulation | |||
Responsed Disease | Pancreatic ductal adenocarcinoma | ICD-11: 2C10.0 | ||
Pathway Response | Ras signaling pathway | hsa04014 | ||
In-vitro Model | HPDE6c7 | Normal | Homo sapiens | CVCL_0P38 |
HEK293T | Normal | Homo sapiens | CVCL_0063 | |
HPAF-II | Pancreatic ductal adenocarcinoma | Homo sapiens | CVCL_0313 | |
MPanc-96 | Pancreatic ductal adenocarcinoma | Homo sapiens | CVCL_7165 | |
PANC-1 | Pancreatic ductal adenocarcinoma | Homo sapiens | CVCL_0480 | |
PaTu 8902 | Pancreatic adenocarcinoma | Homo sapiens | CVCL_1845 | |
PaTu 8988s | Pancreatic adenocarcinoma | Homo sapiens | CVCL_1846 | |
SW1990 | Pancreatic adenocarcinoma | Homo sapiens | CVCL_1723 | |
In-vivo Model | HPAF-II cells (2.0 × 106 cells/site) stably transfected with sh-EGFP or sh-UCA1 were subcutaneously injected into 4-week-old nude mice to generate xenografts. The tumor volume was measured every week after injection and calculated using the following formula: length × (width2)/2. | |||
Pancreatic cancer [ICD-11: 2C10]
In total 1 item(s) under this disease | ||||
Experiment 1 Reporting the m6A-centered Disease Response | [1] | |||
Response Summary | UCA1 increases GTPase KRas (KRAS) phosphorylation by interacting with hnRNPA2B1 and that UCA1 functions as a molecular sponge for miR-590-3p to promote KRAS expression. the UCA1-KRAS axis plays a crucial role in pancreatic ductal adenocarcinoma progression and that UCA1 serves as a target for new PDAC therapies. | |||
Responsed Disease | Pancreatic ductal adenocarcinoma [ICD-11: 2C10.0] | |||
Target Regulator | Heterogeneous nuclear ribonucleoproteins A2/B1 (HNRNPA2B1) | READER | ||
Target Regulation | Up regulation | |||
Pathway Response | Ras signaling pathway | hsa04014 | ||
In-vitro Model | HPDE6c7 | Normal | Homo sapiens | CVCL_0P38 |
HEK293T | Normal | Homo sapiens | CVCL_0063 | |
HPAF-II | Pancreatic ductal adenocarcinoma | Homo sapiens | CVCL_0313 | |
MPanc-96 | Pancreatic ductal adenocarcinoma | Homo sapiens | CVCL_7165 | |
PANC-1 | Pancreatic ductal adenocarcinoma | Homo sapiens | CVCL_0480 | |
PaTu 8902 | Pancreatic adenocarcinoma | Homo sapiens | CVCL_1845 | |
PaTu 8988s | Pancreatic adenocarcinoma | Homo sapiens | CVCL_1846 | |
SW1990 | Pancreatic adenocarcinoma | Homo sapiens | CVCL_1723 | |
In-vivo Model | HPAF-II cells (2.0 × 106 cells/site) stably transfected with sh-EGFP or sh-UCA1 were subcutaneously injected into 4-week-old nude mice to generate xenografts. The tumor volume was measured every week after injection and calculated using the following formula: length × (width2)/2. | |||