Tgm3-flox Mouse
一般名
Tgm3-flox
製品ID
S-CKO-06247
背景情報
C57BL/6JCya
系統ID
CKOCMP-21818-Tgm3-B6J-VA
状況
このマウス系統を論文で使用する場合は、「Tgm3-flox Mouse(カタログ番号S-CKO-06247)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
Tgm3-flox
系統ID
CKOCMP-21818-Tgm3-B6J-VA
遺伝子名
製品ID
S-CKO-06247
遺伝子別名
we, TGE, TG E, TG(E), TGase E, TGase-3
遺伝子別名
C57BL/6JCya
NCBI ID
修正
Conditional 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
ENSMUST00000110299
NCBIトランスクリプトID
NM_009374.3
ターゲット領域
Exon 3~4
有効領域の大きさ
~1.7 kb
遺伝子研究の概要
Tgm3, also known as epidermal TGM, is a pivotal enzyme responsible for the formation of protein polymers in the epidermis and hair follicle, contributing to their protective and barrier functions [5]. It is involved in processes like epidermal keratinocyte differentiation into cornified cells and the hardening of hair follicles and shafts through enzymatic cross-linking of structural proteins and keratin intermediate filaments.
In cancer research, Tgm3 shows diverse roles. In hepatocellular carcinoma (HCC), its overexpression promotes epithelial-mesenchymal transition (EMT), cell proliferation, and metastasis, predicting poor prognosis. Tgm3 knockdown decreased HCC cell proliferation, invasion, and xenograft tumour growth, and inhibited AKT, ERK, p65, and GSK3β/β-catenin activation while promoting cleaved caspase 3 levels [1].
In contrast, in colorectal cancer, cutaneous squamous carcinoma, and head and neck cancer, Tgm3 acts as a tumor suppressor. In colorectal cancer, its down-regulation is associated with tumor invasion, metastasis, and patient prognosis. Tgm3 overexpression suppressed cell proliferation, invasion, and metastasis, inhibited epithelial-to-mesenchymal transition, and activated phosphorylated AKT [2]. In cutaneous squamous carcinoma, Tgm3 expression was increased in well-differentiated tumors, and its loss was associated with poor differentiation and high recurrence. Tgm3 inhibited tumor growth via the PI3K-AKT signaling pathway [3]. In head and neck cancer, Tgm3 was down-regulated, and its exogenous expression inhibited cell proliferation, enhanced apoptosis in vitro, and suppressed tumor growth in vivo [4].
In conclusion, Tgm3 has crucial functions in epithelial differentiation. In cancer, its role varies by cancer type, either promoting or suppressing tumorigenesis. Studies using gene knockdown (a form of functional loss-of-function similar to gene knockout in concept) in different cancer cell lines and in vivo xenograft models have revealed its complex role in cancer-related biological processes, providing potential therapeutic targets for cancers such as HCC, colorectal cancer, cutaneous squamous carcinoma, and head and neck cancer.
References:
1. Hu, Jin-Wu, Yang, Zhang-Fu, Li, Jia, Fan, Jia, Huang, Xiao-Wu. 2019. TGM3 promotes epithelial-mesenchymal transition and hepatocellular carcinogenesis and predicts poor prognosis for patients after curative resection. In Digestive and liver disease : official journal of the Italian Society of Gastroenterology and the Italian Association for the Study of the Liver, 52, 668-676. doi:10.1016/j.dld.2019.10.010. https://pubmed.ncbi.nlm.nih.gov/31822388/
2. Feng, Yifei, Ji, Dongjian, Huang, Yuanjian, Sun, Yueming, Xu, Ziwei. 2020. TGM3 functions as a tumor suppressor by repressing epithelial‑to‑mesenchymal transition and the PI3K/AKT signaling pathway in colorectal cancer. In Oncology reports, 43, 864-876. doi:10.3892/or.2020.7474. https://pubmed.ncbi.nlm.nih.gov/32020212/
3. Zhou, Kaili, Wu, Chenglong, Cheng, Wenjie, Yao, Zhirong, Zhang, Xue. 2024. Transglutaminase 3 regulates cutaneous squamous carcinoma differentiation and inhibits progression via PI3K-AKT signaling pathway-mediated Keratin 14 degradation. In Cell death & disease, 15, 252. doi:10.1038/s41419-024-06626-5. https://pubmed.ncbi.nlm.nih.gov/38589352/
4. Wu, Xiangbing, Cao, Wei, Wang, Xu, Wu, Yadi, Chen, Wantao. 2013. TGM3, a candidate tumor suppressor gene, contributes to human head and neck cancer. In Molecular cancer, 12, 151. doi:10.1186/1476-4598-12-151. https://pubmed.ncbi.nlm.nih.gov/24289313/
5. Chermnykh, Elina S, Alpeeva, Elena V, Vorotelyak, Ekaterina A. 2020. Transglutaminase 3: The Involvement in Epithelial Differentiation and Cancer. In Cells, 9, . doi:10.3390/cells9091996. https://pubmed.ncbi.nlm.nih.gov/32872587/
品質管理基準
精子検査
凍結前の精子濃度を測定し、精子の生存能力の判定します。
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。
環境基準:
SPF対応地域:
グローバル由来:
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