Human SATB2-AS1 qPCR Primer Pair,即人SATB2-AS1 qPCR引物对,主要用于基于SYBR Green的qPCR、One-Step qRT-PCR或semi-quantitative PCR。本引物为预先设计、经过qPCR验证、预混的引物对。 qPCR (Quantitative PCR)即定量PCR,也称实时荧光定量PCR或实时定量PCR (Real-time quantitative PCR)、实时PCR (Real-time ...
胃癌组织中SATB2-AS1表达及临床意义
90%和80. 77%.不同肿瘤直径,TNM分期和分化程度的SATB2-AS1水平比较差异有统计学意义(P<0. 05).SATB2-AS1水平与总生存期(OS)有关,其中337例高水平者的中位OS为36. 4个月,低于294例低水平者的80. 7个月(HR=1. 36,95%CI:1. 09~1. 70,P<0. 05).结论 SATB2-AS1在胃癌组织中高表达,可用于...
Levels of SATB2-AS1, miR-155-3p and breast cancer metastasis suppressor 1-like (BRMS1L) in BC were determined. The prognostic role of SATB2-AS1 in BC patients was assessed. The screened cells were respectively introduced with altered SATB2-AS1 or miR-155-3p to figure out their roles in...
There are comments on PubPeer for publication: Long non-coding RNA SATB2-AS1 inhibits microRNA-155-3p to suppress breast cancer cell growth by promoting breast cancer metastasis suppressor 1-like (2020)
Mechanistically, SATB2-AS1 inactivated STAT3/HIF-1伪 and strengthened GRIM-19 expression. After knocking down GRIM-19 with small interfering RNA (siRNA), the malignant phenotypes of HCC cells were enhanced. Further bioinformatics analysis showed that miR-3678-3p was targeted by SATB2-AS1. The ...
Elevated SATB2-AS1 and inhibited miR-155-3p were able to restrain malignant behaviors of BC cells in vitro, as well as decelerate tumor growth in vivo. Oppositely, inhibited SATB2-AS1 and amplified miR-155-3p had converse effects on BC cell growth. MiR-155-3p mimic abrogated the impact ...
宫颈癌增殖凋亡目的探究长链非编码RNA SATB2-AS1作为内源性竞争RNA调控miR-373-5p/BTG3轴在宫颈癌(cervical cancer,CC)细胞增殖,凋亡中的作用.方法qRT-PCR技术检测CC患者癌旁组织,癌组织中LncRNA SATB2-AS1,miR-373-5p和BTG3的表达水平.预测并验证LncRNA SATB2/miR-373-5p/BTG3之间的相互作用关系.干预细胞...
Retraction Note to: Long non-coding RNA SATB2-AS1 inhibits microRNA-155-3p to suppress breast cancer cell growth by promoting breast cancer metastasis suppressor 1-likeMETASTATIC breast cancerLINCRNACANCER cell growthBREAST cancerThis article has been retracted. Please see the Retraction Notice for ...
The interaction between SATB2AS1 and microRNA (miR)6715p was verified by bioinformatic analysis, reverse transcriptionquantitative PCR, dual luciferase reporter assay and RNA immunoprecipitation assay. The expression levels of the downstream targets of SATB2AS1 were studied by western blotting. Results ...