Psmd2-flox Mouse
Common Name
Psmd2-flox
제품 ID
S-CKO-06168
Backgroud
C57BL/6JCya
품종 계통계통 ID
CKOCMP-21762-Psmd2-B6J-VA
상태
이 마우스 계통을 논문에서 사용할 경우, “Psmd2-flox Mouse (카탈로그 번호 S-CKO-06168)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
Psmd2-flox
품종 계통계통 ID
CKOCMP-21762-Psmd2-B6J-VA
유전자명
제품 ID
S-CKO-06168
유전자 별칭
Tex190, TEG-190, 9430095H01Rik
배경
C57BL/6JCya
NCBI ID
변형 내용
Conditional knockout
염색체
Chr 16
Phenotype
Datasheet
적용 분야
--
품종 계통 설명
Ensembl 전사체 ID
ENSMUST00000007212
NCBI 전사체 ID
NM_134101
타겟 영역
Exon 4~8
유효 영역 크기
~2.4 kb
유전자 연구 개요
Psmd2, encoding 26S proteasome non-ATPase regulatory subunit 2, is a key component of the ubiquitin-proteasome system. This system is crucial for regulating intracellular protein levels, and thus Psmd2 is involved in multiple cellular processes like protein homeostasis. It has been associated with pathways such as the cell cycle, antigen processing and presentation, JAK-STAT, Toll-like receptor, P53 and MAPK signaling pathways [1].
In various cancers, Psmd2 shows oncogenic properties. In bladder cancer, its overexpression promotes cancer progression and is correlated with immune infiltration, with high Psmd2 predicting unfavorable overall survival [1]. In esophageal squamous cell carcinoma, it contributes to cancer progression by repressing autophagy through activating the mTOR pathway via upregulating ASS1 [2]. In lung adenocarcinoma, upregulation of Psmd2 is linked to poor prognosis and immune infiltration, and it has a high mutation frequency [3]. In renal cell carcinoma treated with immune checkpoint and tyrosine kinase inhibitors, Psmd2 overexpression is related to resistance and decreased progression-free survival, along with changes in immune cell infiltration [4]. In nasopharyngeal carcinoma, DNAJA4 suppresses metastasis via Psmd2-mediated MYH9 degradation [5]. In breast cancer, RACK1 enhances β-catenin stability by competitively inhibiting its binding to Psmd2 [6]. In HepG2 cells, Psmd2 promotes proliferation by modulating lipid droplet metabolism [7]. In breast cancer cells, Psmd2 regulates cell proliferation and cell cycle progression by modulating p21 and p27 proteasomal degradation [8].
In conclusion, Psmd2 plays significant roles in multiple biological processes, especially in cancer-related functions. Its overexpression in various cancers promotes tumor progression, affects immune infiltration, and is associated with poor prognosis. The study of Psmd2 using in vivo models helps in understanding its role in disease development, potentially providing new therapeutic targets for cancer treatment.
References:
1. Wang, Song, Wang, He, Zhu, Shaoxing, Wang, Zongping. 2022. PSMD2 promotes the progression of bladder cancer and is correlated with immune infiltration. In Frontiers in oncology, 12, 1058506. doi:10.3389/fonc.2022.1058506. https://pubmed.ncbi.nlm.nih.gov/36505799/
2. Liu, Yachen, Wu, Meng, Xu, Shuxiang, Xu, Yang, Yu, Lili. 2023. PSMD2 contributes to the progression of esophageal squamous cell carcinoma by repressing autophagy. In Cell & bioscience, 13, 67. doi:10.1186/s13578-023-01016-4. https://pubmed.ncbi.nlm.nih.gov/36998052/
3. Zhao, Huihui, Lu, Guojun. 2022. Prognostic Implication and Immunological Role of PSMD2 in Lung Adenocarcinoma. In Frontiers in genetics, 13, 905581. doi:10.3389/fgene.2022.905581. https://pubmed.ncbi.nlm.nih.gov/35754829/
4. Xu, Xianglai, Wang, Jiahao, Wang, Ying, Wang, Jiajun, Guo, Jianming. 2024. PSMD2 overexpression as a biomarker for resistance and prognosis in renal cell carcinoma treated with immune checkpoint and tyrosine kinase inhibitors. In Cellular oncology (Dordrecht, Netherlands), 47, 1943-1956. doi:10.1007/s13402-024-00977-z. https://pubmed.ncbi.nlm.nih.gov/39222176/
5. Zhang, Qun, Feng, Ping, Zhu, Xun-Hua, He, Shi-Wei, Li, Ying-Qing. 2023. DNAJA4 suppresses epithelial-mesenchymal transition and metastasis in nasopharyngeal carcinoma via PSMD2-mediated MYH9 degradation. In Cell death & disease, 14, 697. doi:10.1038/s41419-023-06225-w. https://pubmed.ncbi.nlm.nih.gov/37875476/
6. Tian, Ruinan, Tian, Jianfei, Zuo, Xiaoyan, Niu, Ruifang, Zhang, Fei. 2023. RACK1 facilitates breast cancer progression by competitively inhibiting the binding of β-catenin to PSMD2 and enhancing the stability of β-catenin. In Cell death & disease, 14, 685. doi:10.1038/s41419-023-06191-3. https://pubmed.ncbi.nlm.nih.gov/37848434/
7. Tan, Yanjie, Jin, Yi, Wu, Xiang, Ren, Zhuqing. 2019. PSMD1 and PSMD2 regulate HepG2 cell proliferation and apoptosis via modulating cellular lipid droplet metabolism. In BMC molecular biology, 20, 24. doi:10.1186/s12867-019-0141-z. https://pubmed.ncbi.nlm.nih.gov/31703613/
8. Li, Yunhai, Huang, Jing, Zeng, Beilei, Li, Hongzhong, Ren, Guosheng. 2018. PSMD2 regulates breast cancer cell proliferation and cell cycle progression by modulating p21 and p27 proteasomal degradation. In Cancer letters, 430, 109-122. doi:10.1016/j.canlet.2018.05.018. https://pubmed.ncbi.nlm.nih.gov/29777785/
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
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