Btnl9-flox Mouse
一般名
Btnl9-flox
製品ID
S-CKO-07946
背景情報
C57BL/6JCya
系統ID
CKOCMP-237754-Btnl9-B6J-VA
状況
このマウス系統を論文で使用する場合は、「Btnl9-flox Mouse(カタログ番号S-CKO-07946)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
Btnl9-flox
系統ID
CKOCMP-237754-Btnl9-B6J-VA
遺伝子名
製品ID
S-CKO-07946
遺伝子別名
Btn3, B430208I01, D330012D11Rik
遺伝子別名
C57BL/6JCya
NCBI ID
修正
Conditional knockout
染色体
Chr 11
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
ENSMUST00000046522
NCBIトランスクリプトID
NM_172793
ターゲット領域
Exon 2~4
有効領域の大きさ
~5.8 kb
遺伝子研究の概要
Btnl9, or butyrophilin-like protein 9, is a member of the immunoglobulin families. It has been implicated in immune-related and cancer-related pathways [1]. Functional enrichment analyses suggest its involvement in various biological processes relevant to disease mechanisms.
In multiple cancer types, studies have shown significant associations. In thyroid cancer (THCA), BTNL9 expression is down-regulated, related to tumor stages, immune cell infiltrations, and prognosis, with lower expression associated with a poorer progression-free interval (PFI) [1]. In breast cancer, its down-regulation is common, and ectopic expression inhibits cell proliferation, colony formation, and metastasis, while inducing apoptosis, acting via the P53/CDC25C and P53/GADD45 pathways [2]. In non-small-cell lung cancer, lncRNA CALML3-AS1 drives cancer progression by epigenetically repressing BTNL9 [3]. In uveal melanoma, high BTNL9 expression is associated with a favorable prognosis, and it can suppress invasion [4]. In lung adenocarcinoma, its down-regulation is linked to a poor overall survival probability, and it is positively correlated with immune-related scores and immune cell infiltration levels [5]. In pancreatic cancer, decreased BTNL9 expression is associated with a reduced survival rate [6]. In BRAF-mutated peritoneal metastasis from colorectal cancer, increased expression of BTNL9 is observed [7].
In idiopathic pulmonary fibrosis, BTNL9 is down-regulated, and it may have a protective effect by inhibiting extracellular matrix production and promoting wound repair [8]. In ALS, a negative correlation between BTNL9 and ALS risk was identified through Mendelian randomization analysis [9].
In conclusion, BTNL9 appears to play diverse roles in multiple diseases, especially in various cancers and potentially in neurodegenerative and fibrotic diseases. Its down-regulation is often associated with poor prognosis in cancer, and it is involved in regulating cell proliferation, metastasis, and immune-related processes. These findings from different disease-based studies contribute to understanding its biological functions and potential as a biomarker or therapeutic target.
References:
1. Zhang, Luyao, Yu, Shuang, Hong, Shubin, Li, Yanbing, Xiao, Haipeng. 2023. Comprehensive analysis of BTNL9 as a prognostic biomarker correlated with immune infiltrations in thyroid cancer. In BMC medical genomics, 16, 234. doi:10.1186/s12920-023-01676-8. https://pubmed.ncbi.nlm.nih.gov/37798795/
2. Mo, Qingfan, Xu, Ke, Luo, Chenghao, Wang, Long, Ren, Guosheng. 2021. BTNL9 is frequently downregulated and inhibits proliferation and metastasis via the P53/CDC25C and P53/GADD45 pathways in breast cancer. In Biochemical and biophysical research communications, 553, 17-24. doi:10.1016/j.bbrc.2021.03.022. https://pubmed.ncbi.nlm.nih.gov/33756341/
3. Zhang, Heng, Wang, Shao-Qiang, Zhu, Jie-Bo, Duan, Chao-Jun, Zhang, Chun-Fang. 2023. LncRNA CALML3-AS1 modulated by m6A modification induces BTNL9 methylation to drive non-small-cell lung cancer progression. In Cancer gene therapy, 30, 1649-1662. doi:10.1038/s41417-023-00670-7. https://pubmed.ncbi.nlm.nih.gov/37884580/
4. Jiang, Zhongming, Liu, Fei. 2019. Butyrophilin-Like 9 (BTNL9) Suppresses Invasion and Correlates with Favorable Prognosis of Uveal Melanoma. In Medical science monitor : international medical journal of experimental and clinical research, 25, 3190-3198. doi:10.12659/MSM.914074. https://pubmed.ncbi.nlm.nih.gov/31039142/
5. Ma, Weishuang, Liang, Jiaming, Mo, Junjian, Tian, Dongbo, Chen, Zisheng. 2021. Butyrophilin-like 9 expression is associated with outcome in lung adenocarcinoma. In BMC cancer, 21, 1096. doi:10.1186/s12885-021-08790-9. https://pubmed.ncbi.nlm.nih.gov/34635082/
6. Khojasteh-Leylakoohi, Fatemeh, Mohit, Reza, Khalili-Tanha, Nima, Batra, Jyotsna, Avan, Amir. 2023. Down regulation of Cathepsin W is associated with poor prognosis in pancreatic cancer. In Scientific reports, 13, 16678. doi:10.1038/s41598-023-42928-y. https://pubmed.ncbi.nlm.nih.gov/37794108/
7. Lund-Andersen, Christin, Torgunrud, Annette, Kanduri, Chakravarthi, Larsen, Stein G, Flatmark, Kjersti. 2024. Novel drug resistance mechanisms and drug targets in BRAF-mutated peritoneal metastasis from colorectal cancer. In Journal of translational medicine, 22, 646. doi:10.1186/s12967-024-05467-2. https://pubmed.ncbi.nlm.nih.gov/38982444/
8. Zheng, Peiyan, Sun, Shixue, Wang, Jingxian, Zhang, Xiaohua Douglas, Sun, Baoqing. 2022. Integrative omics analysis identifies biomarkers of idiopathic pulmonary fibrosis. In Cellular and molecular life sciences : CMLS, 79, 66. doi:10.1007/s00018-021-04094-0. https://pubmed.ncbi.nlm.nih.gov/35015148/
9. Lu, Chuan, Huang, Xiao-Xiao, Huang, Ming, Liu, Chaoning, Xu, Jianwen. 2025. Mendelian randomization of plasma proteomics identifies novel ALS-associated proteins and their GO enrichment and KEGG pathway analyses. In BMC neurology, 25, 82. doi:10.1186/s12883-025-04091-x. https://pubmed.ncbi.nlm.nih.gov/40033250/
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