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C57BL/6JCya-Miipem1/Cya
Common Name:
Miip-KO
Product ID:
S-KO-08986
Background:
C57BL/6JCya
Product Type
Age
Genotype
Sex
Quantity
Price:
Contact for Pricing
Basic Information
Strain Name
Miip-KO
Strain ID
KOCMP-28010-Miip-B6J-VB
Gene Name
Miip
Product ID
S-KO-08986
Gene Alias
D4Wsu114e; IIP45
Background
C57BL/6JCya
NCBI ID
28010
Modification
Conventional knockout
Chromosome
4
Phenotype
MGI:106506
Document
Click here to download >>
Application
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More
Rare Disease Data Center >>
Note
Note: When using this mouse strain in a publication, please cite “C57BL/6JCya-Miipem1/Cya mice (Catalog S-KO-08986) were purchased from Cyagen.”
Strain Description
Ensembl Number
ENSMUST00000030886
NCBI RefSeq
NM_001025365
Target Region
Exon 5~8
Size of Effective Region
~2.0 kb
Detailed Document
Click here to download >>
Overview of Gene Research
MIIP, also known as migration and invasion inhibitory protein, is a gene that functions as a tumor-suppressor in various cancers [3]. It plays a role in regulating multiple biological processes. MIIP is involved in pathways related to cell migration, invasion, and mitosis, and is associated with the cytoskeleton system, as it can regulate microtubules by interacting with HDAC6 [3].

In hepatocellular carcinoma (HCC), MIIP expression is decreased, and low MIIP expression is associated with distant metastasis and poor prognosis. MIIP can inhibit the malignant progression of HCC by regulating AKT expression [1]. In colorectal cancer, MIIP down-regulation drives cancer progression through inducing peri-cancerous adipose tissue browning. MIIP interacts with AZGP1, regulating its glycosylation and secretion, which in turn promotes adipose browning and CRC cell proliferation [2]. In triple-negative breast cancer, MIIP is a favorable prognostic indicator, inhibiting tumor angiogenesis, proliferation, and metastasis by interacting with ITGB3 and suppressing its downstream signaling [4]. In clear cell renal cell carcinoma, MIIP inhibits proliferation and angiogenesis via negative modulation of the HIF-2α-CYR61 axis [5]. In prostate cancer, MIIP inhibits EMT and cell invasion through the miR-181a/b-5p-KLF17 axis, and also inhibits growth via interaction with PP1α and negative modulation of AKT signaling [6,8]. In endometrial cancer, MIIP functions as a tumor suppressor, attenuating Rac1 signaling and remodeling the cytoskeleton to suppress metastasis [7]. In nasopharyngeal carcinoma, MIIP expression is associated with radiosensitivity [9]. In esophageal squamous cell carcinoma, MIIP expression is higher in cancer tissues than in paracancerous normal epithelia and is an independent prognostic factor [10].

In conclusion, MIIP plays a crucial role in inhibiting the progression of multiple cancers. Model-based research, especially gene knockout or knockdown experiments in cell lines as described in these studies, has revealed its role in regulating key cellular processes related to cancer development. Understanding MIIP's function provides potential targets for cancer treatment and prognosis prediction.

References:

1. Fang, J, Chen, Y-L, Yao, H-B, Yang, P, Ding, Z-Y. . MIIP inhibits malignant progression of hepatocellular carcinoma through regulating AKT. In European review for medical and pharmacological sciences, 24, 2335-2346. doi:10.26355/eurrev_202003_20500. https://pubmed.ncbi.nlm.nih.gov/32196585/

2. Wang, Qinhao, Su, Yuanyuan, Sun, Ruiqi, Qiao, Qing, Li, Xia. 2024. MIIP downregulation drives colorectal cancer progression through inducing peri-cancerous adipose tissue browning. In Cell & bioscience, 14, 12. doi:10.1186/s13578-023-01179-0. https://pubmed.ncbi.nlm.nih.gov/38245780/

3. Wang, Yingmei, Wen, Jing, Zhang, Wei. . MIIP, a cytoskeleton regulator that blocks cell migration and invasion, delays mitosis, and suppresses tumorogenesis. In Current protein & peptide science, 12, 68-73. doi:. https://pubmed.ncbi.nlm.nih.gov/21190522/

4. Gao, Yujing, Fang, Yujie, Huang, Yongli, Shan, Jingxuan, Li, Pu. 2022. MIIP functions as a novel ligand for ITGB3 to inhibit angiogenesis and tumorigenesis of triple-negative breast cancer. In Cell death & disease, 13, 810. doi:10.1038/s41419-022-05255-0. https://pubmed.ncbi.nlm.nih.gov/36130933/

5. Yan, Fengqi, Wang, Qinhao, Xia, Mingyuan, Wu, Guojun, Li, Xia. . MIIP inhibits clear cell renal cell carcinoma proliferation and angiogenesis via negative modulation of the HIF-2α-CYR61 axis. In Cancer biology & medicine, 19, 818-35. doi:10.20892/j.issn.2095-3941.2020.0296. https://pubmed.ncbi.nlm.nih.gov/34931765/

6. Hu, Wei, Yan, Fengqi, Ru, Yi, Li, Xia, Wang, Qinhao. 2020. MIIP inhibits EMT and cell invasion in prostate cancer through miR-181a/b-5p-KLF17 axis. In American journal of cancer research, 10, 630-647. doi:. https://pubmed.ncbi.nlm.nih.gov/32195032/

7. Wang, Yingmei, Hu, Limei, Ji, Ping, Xue, Fengxia, Zhang, Wei. 2016. MIIP remodels Rac1-mediated cytoskeleton structure in suppression of endometrial cancer metastasis. In Journal of hematology & oncology, 9, 112. doi:10.1186/s13045-016-0342-6. https://pubmed.ncbi.nlm.nih.gov/27760566/

8. Yan, Guang, Ru, Yi, Yan, Fengqi, Wang, Qinhao, Li, Xia. 2019. MIIP inhibits the growth of prostate cancer via interaction with PP1α and negative modulation of AKT signaling. In Cell communication and signaling : CCS, 17, 44. doi:10.1186/s12964-019-0355-1. https://pubmed.ncbi.nlm.nih.gov/31092266/

9. Zhou, Hong-Ping, Qian, Lu-Xi, Zhang, Nan, He, Xia, Yin, Li. 2018. MIIP gene expression is associated with radiosensitivity in human nasopharyngeal carcinoma cells. In Oncology letters, 15, 9471-9479. doi:10.3892/ol.2018.8524. https://pubmed.ncbi.nlm.nih.gov/29805670/

10. Wen, Jing, Liu, Qian-Wen, Luo, Kong-Jia, Hu, Yi, Fu, Jian-Hua. 2016. MIIP expression predicts outcomes of surgically resected esophageal squamous cell carcinomas. In Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine, 37, 10141-8. doi:10.1007/s13277-015-4633-2. https://pubmed.ncbi.nlm.nih.gov/26825982/

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
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