C57BL/6JCya-Fasnem1flox/Cya
Common Name:
Fasn-flox
Product ID:
S-CKO-02363
Background:
C57BL/6JCya
Product Type
Age
Genotype
Sex
Quantity
Price:
Contact for Pricing
Basic Information
Strain Name
Fasn-flox
Strain ID
CKOCMP-14104-Fasn-B6J-VA
Gene Name
Product ID
S-CKO-02363
Gene Alias
A630082H08Rik; FAS
Background
C57BL/6JCya
NCBI ID
Modification
Conditional knockout
Chromosome
11
Phenotype
Document
Application
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Note: When using this mouse strain in a publication, please cite “C57BL/6JCya-Fasnem1flox/Cya mice (Catalog S-CKO-02363) were purchased from Cyagen.”
Strain Description
Ensembl Number
ENSMUST00000055655
NCBI RefSeq
NM_007988
Target Region
Exon 4~8
Size of Effective Region
~1.8 kb
Detailed Document
Overview of Gene Research
Fasn, short for fatty acid synthase, is a key enzyme in lipid metabolism, catalyzing long-chain fatty acid synthesis. It plays a crucial role in de novo fatty acid synthesis, which is important for various biological processes, including cell membrane formation, energy storage, and signal transduction [4].
In multiple cancer types, Fasn has been shown to be a significant contributor. In colorectal cancer, mutations in FBXW7β, an E3 ligase of Fasn, lead to sustained lipogenesis as it can no longer degrade Fasn, promoting cancer growth [1]. In cervical cancer, Fasn promotes lymph node metastasis via cholesterol reprogramming and lymphangiogenesis, and its knockdown or inhibition can reduce metastasis in vivo [2]. In hepatocellular carcinoma, Fasn inhibition increases MHC-I levels, promoting antigen presentation and synergizing with PD-L1 checkpoint blockade to suppress tumor growth [3]. In Clonorchis sinensis infection-related intrahepatic cholangiocarcinoma, Fasn-mediated fatty acid biosynthesis remodels the immune environment, leading to an immunosuppressive state and tumor progression, and Fasn inhibitor treatment can reverse this [4]. In diffuse large B-cell lymphoma, ZDHHC21, a palmitoyltransferase, negatively regulates Fasn by mediating its palmitoylation, and targeting the ZDHHC21/Fasn axis may be a therapeutic strategy [5]. In colorectal cancer, FABP5 interacts with Fasn, activates the ubiquitin-proteasome pathway to decrease Fasn expression, suppressing mTOR signaling and facilitating autophagy, and the Fasn inhibitor orlistat has anti-cancer effects [6]. In intrahepatic cholangiocarcinoma, circRNA MBOAT2 promotes cancer progression by facilitating Fasn mRNA cytoplasmic export, regulating lipid metabolism [7].
In conclusion, Fasn is essential for lipid metabolism. Gene-knockout or conditional-knockout mouse models and other loss-of-function experiments have revealed its significant role in cancer development, metastasis, and immune-related processes. Understanding Fasn's function in these disease areas provides potential therapeutic targets for cancer treatment.
References:
1. Wei, Wenxia, Qin, Baifu, Wen, Weijie, Li, Kai, Lee, Mong-Hong. 2023. FBXW7β loss-of-function enhances FASN-mediated lipogenesis and promotes colorectal cancer growth. In Signal transduction and targeted therapy, 8, 187. doi:10.1038/s41392-023-01405-8. https://pubmed.ncbi.nlm.nih.gov/37202390/
2. Du, Qiqiao, Liu, Pan, Zhang, Chunyu, Liu, Junxiu, Yao, Shuzhong. 2022. FASN promotes lymph node metastasis in cervical cancer via cholesterol reprogramming and lymphangiogenesis. In Cell death & disease, 13, 488. doi:10.1038/s41419-022-04926-2. https://pubmed.ncbi.nlm.nih.gov/35597782/
3. Huang, Jiao, Tsang, Wai Ying, Fang, Xiao-Na, Chan, Yiu Hong, Guan, Xin-Yuan. . FASN Inhibition Decreases MHC-I Degradation and Synergizes with PD-L1 Checkpoint Blockade in Hepatocellular Carcinoma. In Cancer research, 84, 855-871. doi:10.1158/0008-5472.CAN-23-0966. https://pubmed.ncbi.nlm.nih.gov/38486485/
4. Xu, Lixia, Zhang, Ying, Lin, Zhilong, Xie, Yubin, Kuang, Ming. 2024. FASN-mediated fatty acid biosynthesis remodels immune environment in Clonorchis sinensis infection-related intrahepatic cholangiocarcinoma. In Journal of hepatology, 81, 265-277. doi:10.1016/j.jhep.2024.03.016. https://pubmed.ncbi.nlm.nih.gov/38508240/
5. Liu, Bangdong, Zhao, Xianlan, Zhang, Shihao, Zhang, Xi, Rao, Jun. 2024. Targeting ZDHHC21/FASN axis for the treatment of diffuse large B-cell lymphoma. In Leukemia, 38, 351-364. doi:10.1038/s41375-023-02130-5. https://pubmed.ncbi.nlm.nih.gov/38195819/
6. Ye, Mujie, Hu, Chunhua, Chen, Tiaotiao, Tian, Ye, Tang, Qiyun. 2023. FABP5 suppresses colorectal cancer progression via mTOR-mediated autophagy by decreasing FASN expression. In International journal of biological sciences, 19, 3115-3127. doi:10.7150/ijbs.85285. https://pubmed.ncbi.nlm.nih.gov/37416772/
7. Yu, Xiaopeng, Tong, Huanjun, Chen, Jialu, Wang, Shouhua, Tang, Zhaohui. 2023. CircRNA MBOAT2 promotes intrahepatic cholangiocarcinoma progression and lipid metabolism reprogramming by stabilizing PTBP1 to facilitate FASN mRNA cytoplasmic export. In Cell death & disease, 14, 20. doi:10.1038/s41419-022-05540-y. https://pubmed.ncbi.nlm.nih.gov/36635270/
Quality Control Standard
Sperm Test
Pre-cryopreservation: Measurement of sperm concentration, determination of sperm viability.
Post-cryopreservation: A vial of cryopreserved sperms is selected for in-vitro fertilization from each batch.
Environmental Standards:SPF
Available Region:Global
Source:Cyagen