Cenpe-flox Mouse
一般名
Cenpe-flox
製品ID
S-CKO-07295
背景情報
C57BL/6JCya
系統ID
CKOCMP-229841-Cenpe-B6J-VA
状況
このマウス系統を論文で使用する場合は、「Cenpe-flox Mouse(カタログ番号S-CKO-07295)はサイアジェンから購入しました。」と引用してください。
製品タイプ
年齢
遺伝子型
性別
数量
標準的な配送方法では、少なくとも3匹のヘテロ接合体キャリアを保証しています。ホモ接合体キャリアや指定された性別の個体の繁殖サービスも利用可能です。
基本情報
系統名
Cenpe-flox
系統ID
CKOCMP-229841-Cenpe-B6J-VA
遺伝子名
製品ID
S-CKO-07295
遺伝子別名
Kif10, 312kDa, CENP-E, C530022J18
遺伝子別名
C57BL/6JCya
NCBI ID
修正
Conditional knockout
染色体
Chr 3
表現型
アプリケーション
--
さらに
系統詳細
EnsemblトランスクリプトID
ENSMUST00000062893
NCBIトランスクリプトID
NM_173762
ターゲット領域
Exon 2~5
有効領域の大きさ
~2.8 kb
遺伝子研究の概要
Cenpe, short for centromeric protein E, is a microtubule plus-end-directed kinetochore protein, belonging to the centromere protein (CENP) family. It plays a crucial role in mitosis and is involved in cell cycle-related processes. Heterozygous mutations in Cenpe can lead to primary microcephaly syndrome [1,4].
In non-WNT/non-SHH medulloblastoma, Cenpe is highly expressed compared to normal tissues and serves as an independent prognostic factor for survival. Knockdown of Cenpe inhibits cell proliferation by activating the p53 signaling pathway and blocking the cell cycle [1].
In pulmonary hypertension, Cenpe deficiency significantly inhibits the development of pulmonary vascular remodeling and right ventricular hypertrophy, and knocking out Cenpe effectively inhibits the proliferation and induces apoptosis of primary pulmonary artery smooth muscle cells [2].
In cervical cancer, Cenpe expression is upregulated, promoting the progression of cervical squamous cell carcinoma through IL-6-mediated PI3K-Akt and MAPK signaling pathways [3].
In medulloblastoma cells, CENPE knockdown induces mitotic defects, apoptosis, and endogenous DNA damage accumulation, activating TP53 or TP73 as well as cell death signaling pathways [4].
In glioblastoma, Cenpe promotes proliferation by directly binding to WEE1 and regulating the G0-G1 and G2/M phase transitions [5].
In chemoresistant acute myeloid leukemia, knockdown of Cenpe expression suppresses the proliferation of myeloid leukemia cells and reverses cytarabine chemoresistance [6].
In esophageal adenocarcinoma, high Cenpe expression is associated with unfavorable overall survival, and its expression is related to DNA methylation status [7].
In chromophobe renal cell carcinoma, Cenpe is highly expressed and is an important prognostic biomarker, and its function is mainly enriched in proliferation-related pathways [8].
In non-small cell lung cancer, high expression of Cenpe is related to poor prognosis [9].
In lung adenocarcinoma, Cenpe promotes proliferation and is directly regulated by FOXM1 [10].
In conclusion, Cenpe is a key protein in cell cycle-related processes and mitosis. Research using gene-knockout or knockdown models has revealed its significance in various diseases, including different types of cancers and pulmonary hypertension. These findings suggest that Cenpe could be a potential biomarker and therapeutic target for these diseases.
References:
1. Fang, Huangyi, Zhang, Yusong, Lin, Chengyin, Sheng, Hansong, Lin, Jian. 2023. Primary microcephaly gene CENPE is a novel biomarker and potential therapeutic target for non-WNT/non-SHH medulloblastoma. In Frontiers in immunology, 14, 1227143. doi:10.3389/fimmu.2023.1227143. https://pubmed.ncbi.nlm.nih.gov/37593739/
2. Fang, Xiaoyu, Xie, Min, Liu, Xiansheng, He, Yuanzhou. 2021. CENPE contributes to pulmonary vascular remodeling in pulmonary hypertension. In Biochemical and biophysical research communications, 557, 40-47. doi:10.1016/j.bbrc.2021.04.010. https://pubmed.ncbi.nlm.nih.gov/33862458/
3. Peng, Peiqiang, Zheng, Jingying, He, Kang, Zhang, Shuang, Zhao, Lijing. 2024. CENPE is a diagnostic and prognostic biomarker for cervical cancer. In Heliyon, 10, e40860. doi:10.1016/j.heliyon.2024.e40860. https://pubmed.ncbi.nlm.nih.gov/39759304/
4. Iegiani, Giorgia, Gai, Marta, Di Cunto, Ferdinando, Pallavicini, Gianmarco. 2021. CENPE Inhibition Leads to Mitotic Catastrophe and DNA Damage in Medulloblastoma Cells. In Cancers, 13, . doi:10.3390/cancers13051028. https://pubmed.ncbi.nlm.nih.gov/33804489/
5. Ma, Chuanling, Wang, Jianchao, Zhou, Jie, Li, Fangqiong, Zhang, Meng. . CENPE promotes glioblastomas proliferation by directly binding to WEE1. In Translational cancer research, 9, 717-725. doi:10.21037/tcr.2019.11.40. https://pubmed.ncbi.nlm.nih.gov/35117417/
6. Shi, Mingyue, Niu, Junwei, Niu, Xiaona, Chen, Yuqing, Shao, Fengmin. 2021. Lin28A/CENPE Promoting the Proliferation and Chemoresistance of Acute Myeloid Leukemia. In Frontiers in oncology, 11, 763232. doi:10.3389/fonc.2021.763232. https://pubmed.ncbi.nlm.nih.gov/34868981/
7. Zhu, Xueqiang, Luo, Xing, Feng, Gang, Zeng, Ming, Liu, Hao. 2019. CENPE expression is associated with its DNA methylation status in esophageal adenocarcinoma and independently predicts unfavorable overall survival. In PloS one, 14, e0207341. doi:10.1371/journal.pone.0207341. https://pubmed.ncbi.nlm.nih.gov/30716092/
8. Wu, Hui-Feng, Liu, Hao, Zhang, Zhe-Wei, Chen, Ji-Min. 2023. CENPE and LDHA were potential prognostic biomarkers of chromophobe renal cell carcinoma. In European journal of medical research, 28, 481. doi:10.1186/s40001-023-01449-0. https://pubmed.ncbi.nlm.nih.gov/37925501/
9. Hao, Xuezhi, Qu, Tao. 2019. Expression of CENPE and its Prognostic Role in Non-small Cell Lung Cancer. In Open medicine (Warsaw, Poland), 14, 497-502. doi:10.1515/med-2019-0053. https://pubmed.ncbi.nlm.nih.gov/31259255/
10. Shan, Lina, Zhao, Minjie, Lu, Ya, Chai, Wenshu, Shi, Xianbao. 2019. CENPE promotes lung adenocarcinoma proliferation and is directly regulated by FOXM1. In International journal of oncology, 55, 257-266. doi:10.3892/ijo.2019.4805. https://pubmed.ncbi.nlm.nih.gov/31115500/
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凍結後の精子では、各バッチから1本の凍結保存された精子を選び出し、体外受精に使用します。
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