CGR19 antibody Polyclonal Antibodies Primary antibodies
- Known as:
- CGR19 (anti-) Polyclonal Antibodies Primary antibodies
- Catalog number:
- orb100621
- Product Quantity:
- 100
- Category:
- -
- Supplier:
- Biorb
- Gene target:
- CGR19 antibody Polyclonal Antibodies Primary antibodies
Related genes to: CGR19 antibody Polyclonal Antibodies Primary antibodies
- Gene:
- CGRRF1 NIH gene
- Name:
- cell growth regulator with ring finger domain 1
- Previous symbol:
- -
- Synonyms:
- CGR19, RNF197
- Chromosome:
- 14q22.2
- Locus Type:
- gene with protein product
- Date approved:
- 2003-09-29
- Date modifiied:
- 2015-08-24
Related products to: CGR19 antibody Polyclonal Antibodies Primary antibodies
Related articles to: CGR19 antibody Polyclonal Antibodies Primary antibodies
- Previously, Japanese Environmental Mutagen and Genome Society/Mammalian Mutagenicity Study Group/Toxicogenomics Study Group (JEMS/MMS toxicogenomic study group) proposed 12 genotoxic marker genes (Aen, Bax, Btg2, Ccnf, Ccng1, Cdkn1a, Gdf15, Lrp1, Mbd1, Phlda3, Plk2, and Tubb4b) to discriminate genotoxic hepatocarcinogens (GTHCs) from non-genotoxic hepatocarcinogens (NGTHCs) and non-genotoxic non-hepatocarcinogens (NGTNHCs) in mouse and rat liver using qPCR and RNA-Seq and confirmed in public rat toxicogenomics data, Open TG-GATEs, by principal component analysis (PCA). On the other hand, the U.S. Environmental Protection Agency (US EPA) suggested seven genotoxic marker genes (Bax, Btg2, Ccng1, Cgrrf1, Cdkn1a, Mgmt, and Tmem47) with Open TG-GATEs data. Four genes (Bax, Btg2, Ccng1, and Cdkn1a) were common in these two studies. In the present study, we examined the performance of these four genes in Open TG-GATEs data using PCA. - Source: PubMed
Publication date: 2024/12/19
Furihata ChieSuzuki Takayoshi - The KRAS/ERK pathway is crucial in cancer progression and chemotherapy resistance, yet its upstream regulatory mechanism remains elusive. We identified MSI2 as a new promoter of chemotherapy resistance in cancers. MSI2 directly binds to a specific class of mature miRNAs by recognizing the 'UAG' motif and interacts with the essential effector AGO2, highlighting MSI2 as a novel regulatory factor within the miRNA pathway. Specifically, MSI2 recruits UAG-miRNA miR-30a-3p to facilitate its loading onto AGO2, efficiently inhibiting the expression of CGRRF1. Further analysis reveals that CGRRF1 functions as a new ubiquitin E3 ligase for KRAS, mediating the ubiquitination and proteasome degradation of KRAS. Consequently, a novel regulatory axis involving MSI2-AGO2/miR-30a-3p-CGRRF1 positively regulates the KRAS/ERK pathway. Remarkably, platinum-based chemotherapy drugs significantly enhance the levels of phosphorylated ERK1/2 (p-ERK1/2) in cancer cells, and the EGFR inhibitor Gefitinib also increases p-ERK1/2 levels in Gefitinib-resistant cancer cells. Combining small-molecule inhibitors targeting MSI2, such as Ro 08-2750, efficiently alleviated chemoresistance in tumor cells exposed to Platinum and Gefitinib. These findings suggest that MSI2 could be a novel therapeutic target for developing strategies to counteract cancer resistance to treatment. - Source: PubMed
Publication date: 2024/11/09
Lu RunhuiZhang YafanChen RanLi LianHuang CaihuZhou ZihanCao YingtingLi HongyanLi JunyaZhang YixinWang YanliHuang JianZhao XianFeng JingYu JianxiuDu Chunling - - Source: PubMed
Publication date: 2024/08/02
Rong YaoYang WenliYang XiaotongYuan Yuan - Rheumatoid arthritis (RA) is a chronic autoimmune disease characterised by progressive articular damage, functional loss, and comorbidities. The relationship between cuproptosis, a form of programmed cell death, and RA remains unknown. Therefore, this study aimed to explore cuproptosis-related molecular clusters in RA. - Source: PubMed
Publication date: 2023/08/16
Wang AihuaLiu WeiJin YueWei BowenFan YihuaGuo XiaojingGou Xiaoping - CGRRF1 is a growth suppressor and consists of a transmembrane domain and a RING-finger domain. It functions as a RING domain E3 ubiquitin ligase involved in endoplasmic reticulum-associated degradation. The expression of CGRRF1 is decreased in cancer tissues; however, the role of CGRRF1 in breast cancer and the mechanism(s) of its growth suppressor function remain to be elucidated. - Source: PubMed
Publication date: 2019/12/04
Lee Yu-JuHo Shiuh-RongGraves Joshua DXiao YangHuang ShixiaLin Weei-Chin