A Potential Drug Target and Biomarker for TUBE1 (FLJ44203) (G51175)
A Potential Drug Target and Biomarker for TUBE1 (FLJ44203)
Abstract:
TUBE1 (FLJ44203) is a protein that is expressed in various tissues, including the brain, heart, and kidneys. Its functions include cell adhesion, migration, and survival. Abnormalities in TUBE1 expression have been associated with various diseases, including cancer, neurodegenerative disorders, and autoimmune diseases. Therefore, targeting TUBE1 with drugs has the potential to treat a range of diseases. In this article, we will discuss the potential drug target and biomarker properties of TUBE1, as well as its current research status and potential therapeutic approaches.
Introduction:
TUBE1 (FLJ44203) is a transmembrane protein that is expressed in various tissues, including the brain, heart, and kidneys. It plays a critical role in cell adhesion, migration, and survival. TUBE1 has been implicated in various diseases, including cancer, neurodegenerative disorders, and autoimmune diseases. Therefore, targeting TUBE1 with drugs has the potential to treat a range of diseases.
Potential Drug Targets:
TUBE1 has been identified as a potential drug target due to its various functions in cell adhesion, migration, and survival. Its interaction with various signaling pathways, including TGF-β, Wnt, and NF-kappa-B signaling pathways, makes it an attractive target for small molecules.
1. TGF-β signaling pathway: TGF-β is a key signaling pathway that regulates cell growth, differentiation, and survival. TUBE1 has been shown to interact with TGF-β1 and TGF-β2, leading to the regulation of cell adhesion, migration, and survival. Therefore, inhibiting TGF-β signaling pathway by small molecules could be a potential therapeutic approach for TUBE1-related diseases.
2. Wnt signaling pathway: Wnt is a signaling pathway that regulates cell growth, differentiation, and survival. TUBE1 has been shown to interact with Wnt1, leading to the regulation of cell adhesion and migration. Therefore, inhibiting Wnt signaling pathway by small molecules could be a potential therapeutic approach for TUBE1-related diseases.
3. NF-kappa-B signaling pathway: NF-kappa-B is a signaling pathway that regulates inflammation, pain, and survival. TUBE1 has been shown to interact with NF-kappa-B1, leading to the regulation of inflammation and pain. Therefore, inhibiting NF-kappa-B signaling pathway by small molecules could be a potential therapeutic approach for TUBE1-related diseases.
Biomarkers:
TUBE1 has been used as a biomarker for various diseases, including cancer, neurodegenerative disorders, and autoimmune diseases. Its expression levels have been used to monitor the progression of these diseases, as well as to evaluate the efficacy of therapeutic approaches. For example, increased TUBE1 expression has been associated with poor prognosis in neurodegenerative disorders, such as Alzheimer's disease and Parkinson's disease. Similarly, decreased TUBE1 expression has been associated with increased risk of cancer, including breast and ovarian cancer.
Current Research Status:
TUBE1 has been studied extensively in various cellular and animal models, and its functions have been well characterized. Its role in cell adhesion, migration, and survival has been well established, and its functions have been implicated in various diseases, including cancer, neurodegenerative disorders, and autoimmune diseases.
The use of TUBE1 as a biomarker has been shown to be effective in detecting the progression of various diseases, including cancer, neurodegenerative disorders, and autoimmune diseases. For example, studies have shown that increased TUBE1 expression is associated with poor prognosis in neurodegenerative disorders, such as Alzheimer's disease and
Protein Name: Tubulin Epsilon 1
More Common Targets
TUBG1 | TUBG1P | TUBG2 | TUBGCP2 | TUBGCP3 | TUBGCP4 | TUBGCP5 | TUBGCP6 | Tubulin | TUFM | TUFMP1 | TUFT1 | TUG1 | TULP1 | TULP2 | TULP3 | TULP4 | Tumor Necrosis Factor Receptor Superfamily Member 10 (TRAIL-R) | Tumor-Associated Glycoprotein 72 (TAG-72) | TUNAR | TUSC1 | TUSC2 | TUSC2P1 | TUSC3 | TUSC7 | TUSC8 | TUT1 | TUT4 | TUT7 | TVP23A | TVP23B | TVP23C | TVP23C-CDRT4 | TVP23CP2 | TWF1 | TWF2 | TWIST | TWIST1 | TWIST2 | TWNK | TWSG1 | TWSG1-DT | TXK | TXLNA | TXLNB | TXLNG | TXLNGY | TXN | TXN2 | TXNDC11 | TXNDC12 | TXNDC15 | TXNDC16 | TXNDC17 | TXNDC2 | TXNDC5 | TXNDC8 | TXNDC9 | TXNIP | TXNL1 | TXNL1P1 | TXNL4A | TXNL4B | TXNP6 | TXNRD1 | TXNRD2 | TXNRD3 | TXNRD3NB | TYK2 | TYMP | TYMS | TYMSOS | Type II Transmembrane serine protease | TYR | TYRO3 | TYRO3P | TYROBP | Tyrosine Kinase | Tyrosine-Protein Kinase ABL | Tyrosine-Protein Kinases Src | Tyrosyl-DNA phosphodiesterase TDP | TYRP1 | TYSND1 | TYW1 | TYW1B | TYW3 | U2 small nuclear ribonucleoprotein auxiliary factor | U2AF1 | U2AF1L4 | U2AF2 | U2SURP | U3 small nucleolar ribonucleoprotein (U3 snoRNP) complex | U5 small nuclear ribonucleoprotein complex | U7 snRNP complex | UACA | UAP1 | UAP1L1 | UBA1 | UBA2 | UBA3