Ptgds-KO Mouse
一般名
Ptgds-KO
製品ID
S-KO-18883
背景情報
C57BL/6JCya
系統ID
KOCMP-19215-Ptgds-B6J-VB
状況
このマウス系統を論文で使用する場合は、「Ptgds-KO Mouse(カタログ番号S-KO-18883)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
Ptgds-KO
系統ID
KOCMP-19215-Ptgds-B6J-VB
遺伝子名
製品ID
S-KO-18883
遺伝子別名
PGD2, PGDS, 21kDa, PGDS2, Ptgs3, L-PGDS
遺伝子別名
C57BL/6JCya
NCBI ID
修正
Conventional knockout
染色体
Chr 2
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
ENSMUST00000015234
NCBIトランスクリプトID
NM_008963
ターゲット領域
Exon 2~3
有効領域の大きさ
~0.3 kb
遺伝子研究の概要
Ptgds, or prostaglandin D2 synthase, is a glycoprotein belonging to the lipocalin superfamily. It plays dual roles in prostaglandins metabolism and lipid transport, and is involved in various cellular processes [1,2]. It may be associated with pathways like Wnt-β-catenin-STAT3, and has significance in biological processes related to cell proliferation, apoptosis, and cell cycle regulation [1].
In multiple cancers, its role has been explored. In diffuse large B-cell lymphoma (DLBCL), high Ptgds expression correlated with poor prognosis, and its knockdown or treatment with inhibitor AT56 exerted anti-tumor effects by regulating cell functions and enhancing drug sensitivity, possibly through MYH9-mediated regulation of Wnt-β-catenin-STAT3 signaling [1]. In peripheral T cell lymphoma (PTCL), high Ptgds expression was linked to poor prognosis, and its knockdown and AT56 treatment inhibited PTCL progression and promoted ferroptosis by regulating HMOX1-mediated iron metabolism [3]. In cervical squamous cell carcinoma, PTGDS showed low expression, and it was an independent prognostic indicator [4]. In medulloblastoma, low PTGDS expression was associated with a lower 3-year survival rate [5]. In endometrial cancer, decreased PTGDS expression predicted poor survival, and it may be involved in the adaptive immune response, leukocyte migration, and regulation of cell adhesion molecules and chemokine signaling [6]. In prostate adenocarcinoma, overexpression of PTGDS suppressed cell migration, invasion, and proliferation [7]. Also, in aminoglycoside-induced vestibular dysfunction, Ptgds knockdown protected vestibular hair cells [2]. In a Parkinson's disease mouse model, MLKL deficiency led to downregulated Ptgds expression, reduced microglial cells, and dampened neuron death [8]. In rosacea, knockdown of Ptgds in fibroblasts blocked rosacea development in mice [9].
In summary, Ptgds is involved in diverse biological processes with implications in multiple disease areas. Gene knockdown and inhibitor studies, similar to those in KO mouse models, have revealed its roles in cancer progression, vestibular hair cell protection, and neurodegenerative disease-related inflammation. Understanding Ptgds can potentially offer new therapeutic strategies for these diseases.
References:
1. Hu, Shunfeng, Ren, Shuai, Cai, Yiqing, Zhou, Xiangxiang, Wang, Xin. 2021. Glycoprotein PTGDS promotes tumorigenesis of diffuse large B-cell lymphoma by MYH9-mediated regulation of Wnt-β-catenin-STAT3 signaling. In Cell death and differentiation, 29, 642-656. doi:10.1038/s41418-021-00880-2. https://pubmed.ncbi.nlm.nih.gov/34743203/
2. Chen, Chen, Zhao, Zhimin, Han, Jinghong, Zhang, Yue, Nie, Guohui. 2025. Ptgds downregulation protect vestibular hair cells from aminoglycoside-induced vestibulotoxicity. In PloS one, 20, e0320634. doi:10.1371/journal.pone.0320634. https://pubmed.ncbi.nlm.nih.gov/40198625/
3. Hu, Shunfeng, Liu, Bingyu, Shang, Juanjuan, Zhou, Xiangxiang, Wang, Xin. 2024. Targeting PTGDS Promotes ferroptosis in peripheral T cell lymphoma through regulating HMOX1-mediated iron metabolism. In British journal of cancer, 132, 384-400. doi:10.1038/s41416-024-02919-w. https://pubmed.ncbi.nlm.nih.gov/39706989/
4. Jiang, Pinping, Cao, Ying, Gao, Feng, Xie, Manxin, Fu, Shilong. 2021. SNX10 and PTGDS are associated with the progression and prognosis of cervical squamous cell carcinoma. In BMC cancer, 21, 694. doi:10.1186/s12885-021-08212-w. https://pubmed.ncbi.nlm.nih.gov/34116656/
5. Ren, Zhangping, Gao, Ming, Jiang, Wei. 2022. Prognostic role of NLGN2 and PTGDS in medulloblastoma based on gene expression omnibus. In American journal of translational research, 14, 3769-3782. doi:. https://pubmed.ncbi.nlm.nih.gov/35836891/
6. Zou, Ruoyao, Zheng, Mingjun, Tan, Mingzi, Luan, Nannan, Zhu, Liancheng. 2020. Decreased PTGDS Expression Predicting Poor Survival of Endometrial Cancer by Integrating Weighted Gene Co-Expression Network Analysis and Immunohistochemical Validation. In Cancer management and research, 12, 5057-5075. doi:10.2147/CMAR.S255753. https://pubmed.ncbi.nlm.nih.gov/32617019/
7. Chen, Bohong, Guo, Li, Wang, Lihui, Wu, Dapeng, Du, Yuefeng. 2024. Leveraging cell death patterns to predict metastasis in prostate adenocarcinoma and targeting PTGDS for tumor suppression. In Scientific reports, 14, 21680. doi:10.1038/s41598-024-72985-w. https://pubmed.ncbi.nlm.nih.gov/39289451/
8. Geng, Lu, Gao, Wenqing, Saiyin, Hexige, Zhang, Zhuohua, Li, Jixi. 2023. MLKL deficiency alleviates neuroinflammation and motor deficits in the α-synuclein transgenic mouse model of Parkinson's disease. In Molecular neurodegeneration, 18, 94. doi:10.1186/s13024-023-00686-5. https://pubmed.ncbi.nlm.nih.gov/38041169/
9. Chen, Mengting, Yang, Li, Zhou, Peijie, Deng, Zhili, Li, Ji. 2024. Single-cell transcriptomics reveals aberrant skin-resident cell populations and identifies fibroblasts as a determinant in rosacea. In Nature communications, 15, 8737. doi:10.1038/s41467-024-52946-7. https://pubmed.ncbi.nlm.nih.gov/39384741/
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