Target Name: PRAMEF9
NCBI ID: G343070
Review Report on PRAMEF9 Target / Biomarker Content of Review Report on PRAMEF9 Target / Biomarker
PRAMEF9
Other Name(s): PRAME family member 9 | PRAME family member 9/15

PRAMEF9: A Potential Drug Target and Biomarker

Pramef9, also known as PRAMEF9-1, is a protein that belongs to the PRAME family, which is a group of proteins that are characterized by the presence of a specific domain called the PRAME domain. This domain is known for its ability to interact with various signaling pathways, including the TGF-β pathway. PRAMEF9 has been shown to play a role in several cellular processes, including cell adhesion, migration, and invasion. As a result, PRAMEF9 has emerged as a potential drug target and biomarker.

The TGF-β pathway is a well-established signaling pathway that plays a critical role in several cellular processes, including cell growth, differentiation, and inflammation. The pathway is composed of several transcription factors, including SMAD1, SMAD4, TGF-β1, and TGF-β2. These transcription factors can bind to specific DNA sequences to regulate the expression of target genes.

PRAMEF9 is a protein that has been shown to interact with the TGF-β pathway. This interaction occurs through the PRAME domain, which is a conserved region that is found in several proteins that belong to the PRAME family. The PRAME domain is known for its ability to interact with various signaling pathways, including the TGF-β pathway. This interaction between PRAMEF9 and the TGF-β pathway suggests that PRAMEF9 may be a drug target that can be targeted with compounds that can modulate the activity of the TGF-β pathway.

In addition to its potential role as a drug target, PRAMEF9 has also been shown to be a potential biomarker. The TGF-β pathway is involved in several cellular processes that are critical for cancer progression, including the development of tumors, the angiogenesis of tumors, and the maintenance of cancer stem cells. As a result, changes in the activity of the TGF-β pathway have been associated with the development and progression of many types of cancer.

PRAMEF9 has been shown to play a role in regulating the activity of the TGF-β pathway in several cellular processes. For example, studies have shown that PRAMEF9 can inhibit the activity of the TGF-β pathway, which can lead to the inhibition of cell proliferation and the suppression of the development of cancer stem cells. Additionally, PRAMEF9 has been shown to promote the degradation of the TGF-β pathway transcription factor, SMAD1, which can lead to the deletion of TGF-β1 and TGF-β2, which are critical for the development of cancer.

The potential drug targets for PRAMEF9 are vast, and there are several different approaches that can be used to target the protein. One approach is to use small molecules that can modulate the activity of the TGF-β pathway. This can be done by binding to specific PRAMEF9 domains, such as the N-terminus or the A-terminus, or by binding to proteins that interact with PRAMEF9 and modulating the activity of the TGF-β pathway.

Another approach to targeting PRAMEF9 is to use antibodies that recognize specific PRAMEF9 proteins. This can be done by using antibodies that recognize the PRAMEF9 protein and then using these antibodies to block the activity of the protein. This approach can be useful for studying the molecular mechanisms underlying the activity of PRAMEF9 and for identifying potential drug targets.

In conclusion, PRAMEF9 is a protein that has been shown to interact with the TGF-β pathway and has the potential to be a drug target or biomarker. Further research is needed to fully understand the role of PRAMEF9 in cellular processes and to identify potential drug targets. If successful, PRAMEF9 may be a valuable tool for the development of new cancer therapies.

Protein Name: PRAME Family Member 9

The "PRAMEF9 Target / Biomarker Review Report" is a customizable review of hundreds up to thousends of related scientific research literature by AI technology, covering specific information about PRAMEF9 comprehensively, including but not limited to:
•   general information;
•   protein structure and compound binding;
•   protein biological mechanisms;
•   its importance;
•   the target screening and validation;
•   expression level;
•   disease relevance;
•   drug resistance;
•   related combination drugs;
•   pharmacochemistry experiments;
•   related patent analysis;
•   advantages and risks of development, etc.
The report is helpful for project application, drug molecule design, research progress updates, publication of research papers, patent applications, etc. If you are interested to get a full version of this report, please feel free to contact us at BD@silexon.ai

More Common Targets

PRANCR | PRAP1 | PRB1 | PRB2 | PRB3 | PRB4 | PRC1 | PRC1-AS1 | PRCC | PRCD | PRCP | PRDM1 | PRDM10 | PRDM10-DT | PRDM11 | PRDM12 | PRDM13 | PRDM14 | PRDM15 | PRDM16 | PRDM16-DT | PRDM2 | PRDM4 | PRDM5 | PRDM6 | PRDM7 | PRDM8 | PRDM9 | PRDX1 | PRDX2 | PRDX2P4 | PRDX3 | PRDX4 | PRDX5 | PRDX6 | Pre-mRNA cleavage complex II | PREB | PRECSIT | Prefoldin complex | PRELID1 | PRELID1P6 | PRELID2 | PRELID3A | PRELID3B | PRELP | Prenyl diphosphate synthase | Prenyltransferase | PREP | PREPL | Presenilin | PREX1 | PREX2 | PRF1 | PRG1 | PRG2 | PRG3 | PRG4 | PRH1 | PRH1-PRR4 | PRH1-TAS2R14 | PRH2 | PRICKLE1 | PRICKLE2 | PRICKLE2-AS1 | PRICKLE2-AS2 | PRICKLE3 | PRICKLE4 | PRIM1 | PRIM2 | PRIM2BP | PRIMA1 | PRIMPOL | PRINS | PRKAA1 | PRKAA2 | PRKAB1 | PRKAB2 | PRKACA | PRKACB | PRKACG | PRKAG1 | PRKAG2 | PRKAG2-AS1 | PRKAG2-AS2 | PRKAG3 | PRKAR1A | PRKAR1B | PRKAR2A | PRKAR2A-AS1 | PRKAR2B | PRKCA | PRKCA-AS1 | PRKCB | PRKCD | PRKCE | PRKCG | PRKCH | PRKCI | PRKCQ | PRKCQ-AS1