General Information of the m6A Target Gene (ID: M6ATAR00477)
Target Name Small nucleolar RNA host gene 3 (SNHG3)
Synonyms
RNU17D; RNU17C; Previous names; RNA, U17D small nucleolar; RNA, U17C small nucleolar; small nucleolar RNA host gene 3 (non-protein coding); Alias symbols; U17HG; U17HG-A; NCRNA00014; Alias names; non-protein coding RNA 14
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Gene Name SNHG3
Chromosomal Location 1p35.3
Family Small nucleolar RNA non-coding host genes
Gene ID 8420
HGNC ID
HGNC:10118
Ensembl Gene ID
ENSG00000242125
Full List of m6A Methylation Regulator of This Target Gene and Corresponding Disease/Drug Response(s)
SNHG3 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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Methyltransferase-like 3 (METTL3) [WRITER]
Representative RIP-seq result supporting the interaction between SNHG3 and the regulator
Cell Line MDA-MB-231 Homo sapiens
Regulation logFC: 1.17E+00 GSE60213
In total 1 item(s) under this regulator
Experiment 1 Reporting the m6A Methylation Regulator of This Target Gene [1]
Response Summary Platinum can increase the overall m6A level of esophageal cancer. Small nucleolar RNA host gene 3 (SNHG3)/miR-186-5p, induced by platinum, was involved in regulating m6A level by targeting METTL3. miR-186-5p binds to the 3'UTR of METTL3 to inhibit its expression. Our manuscript has provided clues that regulating m6A level was a novel way to enhance the platinum efficacy.
Target Regulation Up regulation
Responsed Disease Esophageal cancer ICD-11: 2B70
Responsed Drug Pt Investigative
Cell Process Cellular Processes
Cell growth and death
Cell apoptosis
In-vitro Model Eca-9706 (Esophageal carcinoma cell line)
KYSE-150 Esophageal squamous cell carcinoma Homo sapiens CVCL_1348
In-vivo Model Used 1 × 106 SNHG3 knocked down KY-SE150 cells and NC lentivirus to inject into the right flank of mice to generate xenografts.
Esophageal cancer [ICD-11: 2B70]
In total 1 item(s) under this disease
Experiment 1 Reporting the m6A-centered Disease Response [1]
Response Summary Platinum can increase the overall m6A level of esophageal cancer. Small nucleolar RNA host gene 3 (SNHG3)/miR-186-5p, induced by platinum, was involved in regulating m6A level by targeting METTL3. miR-186-5p binds to the 3'UTR of METTL3 to inhibit its expression. Our manuscript has provided clues that regulating m6A level was a novel way to enhance the platinum efficacy.
Responsed Disease Esophageal cancer [ICD-11: 2B70]
Target Regulator Methyltransferase-like 3 (METTL3) WRITER
Target Regulation Up regulation
Responsed Drug Pt Investigative
Cell Process Cellular Processes
Cell growth and death
Cell apoptosis
In-vitro Model Eca-9706 (Esophageal carcinoma cell line)
KYSE-150 Esophageal squamous cell carcinoma Homo sapiens CVCL_1348
In-vivo Model Used 1 × 106 SNHG3 knocked down KY-SE150 cells and NC lentivirus to inject into the right flank of mice to generate xenografts.
Pt [Investigative]
In total 1 item(s) under this drug
Experiment 1 Reporting the m6A-centered Drug Response [1]
Response Summary Platinum can increase the overall m6A level of esophageal cancer. Small nucleolar RNA host gene 3 (SNHG3)/miR-186-5p, induced by platinum, was involved in regulating m6A level by targeting METTL3. miR-186-5p binds to the 3'UTR of METTL3 to inhibit its expression. Our manuscript has provided clues that regulating m6A level was a novel way to enhance the platinum efficacy.
Target Regulator Methyltransferase-like 3 (METTL3) WRITER
Target Regulation Up regulation
Responsed Disease Esophageal cancer ICD-11: 2B70
Cell Process Cellular Processes
Cell growth and death
Cell apoptosis
In-vitro Model Eca-9706 (Esophageal carcinoma cell line)
KYSE-150 Esophageal squamous cell carcinoma Homo sapiens CVCL_1348
In-vivo Model Used 1 × 106 SNHG3 knocked down KY-SE150 cells and NC lentivirus to inject into the right flank of mice to generate xenografts.
References
Ref 1 Targeting SNHG3/miR-186-5p reverses the increased m6A level caused by platinum treatment through regulating METTL3 in esophageal cancer. Cancer Cell Int. 2021 Feb 17;21(1):114. doi: 10.1186/s12935-021-01747-9.