Tgm3-flox Mouse
Common Name
Tgm3-flox
제품 ID
S-CKO-06247
Backgroud
C57BL/6JCya
품종 계통계통 ID
CKOCMP-21818-Tgm3-B6J-VA
상태
이 마우스 계통을 논문에서 사용할 경우, “Tgm3-flox Mouse (카탈로그 번호 S-CKO-06247)은 Cyagen에서 구입하였습니다.”라고 명시해 주시기 바랍니다.
구매 가능한 제품 종류
연령
Genotype
성별
수량
표준 제공 조건은 최소 3마리의 이형접합(heterozygous) 보균자를 보장합니다. 동형접합(homozygous) 보균자 및/또는 특정 성별에 대한 브리딩 서비스도 제공됩니다.
기본 정보
품종 계통
Tgm3-flox
품종 계통계통 ID
CKOCMP-21818-Tgm3-B6J-VA
유전자명
제품 ID
S-CKO-06247
유전자 별칭
we, TGE, TG E, TG(E), TGase E, TGase-3
배경
C57BL/6JCya
NCBI ID
변형 내용
Conditional knockout
염색체
Chr 2
Phenotype
Datasheet
적용 분야
--
품종 계통 설명
Ensembl 전사체 ID
ENSMUST00000110299
NCBI 전사체 ID
NM_009374.3
타겟 영역
Exon 3~4
유효 영역 크기
~1.7 kb
유전자 연구 개요
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/
품질 관리 기준
정자 검사
동결 보존 전: 정자 농도 측정 및 정자 생존율 평가.
동결 보존 후: 각 배치에서 동결 보존된 정자 바이알 1개를 선택하여 체외수정(in vitro fertilization)에 사용합니다.
Environmental Standards:
SPFAvailable Region:
GlobalSource:
Cyagen문의하기
맞춤형 동물 모델 관련 상담을 위해 Cyagen 전문가와 연락해 보세요. 아래 양식을 작성하여 상담을 시작하거나 견적을 요청하시기 바랍니다.
Cyagen은 고객님의 개인정보를 소중히 여깁니다. 최신 제품, 서비스 및 인사이트를 안내드리고자 합니다. 고객님의 수신 설정은 다음과 같습니다:
해당 커뮤니케이션은 언제든지 수신 거부하실 수 있습니다. 수신 거부 방법 및 데이터 보호에 대한 자세한 내용은 개인정보처리방침을 참고해 주시기 바랍니다.
아래 버튼을 클릭함으로써, 요청하신 콘텐츠 제공을 위해 본 양식을 통해 제출된 개인정보를 Cyagen이 저장 및 처리하는 데 동의하게 됩니다.
