Metadherin Proteine (MTDH)

Mouse (Murine) Metadherin (MTDH) Interaktionspartner

1. Data show MTDH mRNA expression upregulated in cervical cancer tissues and inversely correlated with miR (zeige MLXIP Proteine)-433 expression. Its knockdown showed similar tumor-suppressive roles as miR (zeige MLXIP Proteine)-433 overexpression in regards to cervical cancer cell proliferation, invasion and apoptosis. MTDH overexpression markedly reversed the effects of miR (zeige MLXIP Proteine)-433 overexpression in regards to proliferation, invasion and of cervical cancer cells.

2. Up regulation of AEG protein plays a role in the pathogenesis of NAFLD.

3. miR (zeige MLXIP Proteine)-26a is capable of suppressing the proliferation and migration of ESCC cells via negative regulation of metadherin

4. Mtdh is a potent modulator of podocyte apoptosis.

5. AEG-1 thus might play a role in NTIS associated with HCC (zeige FAM126A Proteine) and other cancers.

6. When fed a high fat and cholesterol diet (HFD), WT mice rapidly gained weight, whereas AEG-1 KO mice did not gain weight at all.

7. MTDH has a critical role in male fertility and the DNA repair mechanisms required for normal spermatogenesis

8. Data provide evidence that MTDH has a functional role in the progression and metastatic spread of ovarian cancer.

9. RNA-sequencing analysis identified a unique gene signature in livers of Alb (zeige ALB Proteine)/AEG-1/c-Myc (zeige MYC Proteine) mice that was not observed when either AEG-1 or c-Myc (zeige MYC Proteine) was overexpressed

10. Findings establish a pivotal role for MTDH in prostate cancer progression and metastasis.

Human Metadherin (MTDH) Interaktionspartner

1. Reduction of TUG1 level suppressed cell growth and metastasis by regulating AEG1 expression mediated by targeting miR (zeige MLXIP Proteine)-129-5p.

2. miR96 may impede the epithelial to mesenchymal transition process by downregulating AEG1 in glioblastoma cancer cells.

3. The findings demonstrated that miR (zeige MLXIP Proteine)-379 may play tumor-suppressing roles in glioma through downregulation of MTDH and regulation of the PTEN/AKT (zeige AKT1 Proteine) signaling pathway.

4. High AEG1 expression was associated with Oral Squamous Cell Carcinomas.

5. miR675 expression was downregulated in melanoma tissues and cell lines. Functional assays demonstrated that the upregulation of miR675 impaired cell proliferation and invasion in melanoma. Bioinformatics analysis, luciferase reporter assay, reverse transcriptionquantitative polymerase chain reaction and western blot analysis demonstrated that metadherin (MTDH) was a direct target of miR675 in melanoma.

6. Our findings provided evidence that AEG-1 contributed to the production of inflammatory cytokines, migration and invasion of rheumatoid arthritis fibroblast-like synoviocytes, and underscored the importance of AEG-1 in the inflammation process of rheumatoid arthritis

7. High MTDH expression is associated with gastric cancer metastasis.

8. Knockdown of MTDH expression also upregulated PTEN and suppressed pAKT (zeige AKT1 Proteine) protein expression in Caki2 cells. In conclusion, the present study is the first, to the best of our knowledge, to provide evidence suggesting that miRNA30a5p suppresses tumor human renal cancer cell proliferation via the MTDH/PTEN/AKT (zeige AKT1 Proteine) pathway

9. These results suggested that miR216b acted as a tumor suppressor in glioma by directly targeting MTDH and that the miR216b/MTDH axis may be an effective therapeutic target for the treatment of patients with this disease

10. AEG-1 functions as a selective endoplasmic reticulum mRNA-binding protein.