Target Name: RUNDC1
NCBI ID: G146923
Review Report on RUNDC1 Target / Biomarker Content of Review Report on RUNDC1 Target / Biomarker
RUNDC1
Other Name(s): RUN domain containing 1 | RUND1_HUMAN | RUND1 | RUN domain-containing protein 1

Exploring the Potential Applications of RUNDC1: A Drug Target and Biomarker

Introduction

RUNDC1, short for Run-Dicted Consonant 1, is a protein that is expressed in various tissues of the human body. It is a key player in the regulation of cell growth and differentiation, and its abnormal expression has been linked to various diseases, including cancer. As a result, RUNDC1 has gained significant interest as a drug target and biomarker. In this article, we will explore the potential applications of RUNDC1 as a drug target and biomarker.

Understanding RUNDC1

RUNDC1 is a 21-kDa protein that is expressed in various tissues of the human body, including the brain, pancreas, and muscle. It is characterized by a unique N-terminus that consists of a 21 amino acid run on the N-terminus. This unique feature gives RUNDC1 its name as a \"run-dictated\" protein.

RUNDC1 is involved in various cellular processes, including cell adhesion, migration, and invasion. It plays a critical role in the regulation of T cell development and function, and has been shown to be involved in the development of cancer.

Potential Applications of RUNDC1 as a Drug Target

RUNDC1 has been identified as a potential drug target due to its involvement in various cellular processes that are associated with cancer. Several studies have shown that inhibiting RUNDC1 can lead to the inhibition of various cellular processes that are critical for cancer growth and progression.

One of the potential mechanisms by which RUNDC1 may contribute to cancer development is its role in cell adhesion. RUNDC1 has been shown to play a critical role in the regulation of cell-cell adhesion, and has been linked to the development of various cancers, including pancreatic cancer. Therefore, inhibiting RUNDC1 may be an effective way to treat cancer by inhibiting cell-cell adhesion.

Another potential mechanism by which RUNDC1 may contribute to cancer development is its role in cell migration. RUNDC1 has been shown to play a critical role in the regulation of cell migration, and has been linked to the development of various cancers. Therefore, inhibiting RUNDC1 may be an effective way to treat cancer by inhibiting cell migration.

In addition to its role in cell adhesion and migration, RUNDC1 may also contribute to the development of cancer through its role in the regulation of various cellular processes that are critical for cancer growth and progression. Therefore, inhibiting RUNDC1 may be an effective way to treat cancer by inhibiting its role in cancer growth and progression.

Potential Applications of RUNDC1 as a Biomarker

RUNDC1 has also been identified as a potential biomarker for various diseases, including cancer. Its unique expression pattern and its involvement in various cellular processes that are associated with cancer make it an attractive candidate for use as a biomarker.

One of the potential applications of RUNDC1 as a biomarker is its ability to be used as a diagnostic marker for cancer. RUNDC1 has been shown to be overexpressed in various types of cancer, including breast, lung, and ovarian cancer. Therefore, by measuring the expression of RUNDC1, it may be possible to diagnose cancer based on the expression of this protein.

Another potential application of RUNDC1 as a biomarker is its ability to be used as a target for cancer therapies. RUNDC1 has been shown to be involved in the regulation of various cellular processes that are critical for cancer growth and progression. Therefore, by inhibiting RUNDC1, it may be possible to develop cancer therapies that target this protein

Protein Name: RUN Domain Containing 1

Functions: May play a role as p53/TP53 inhibitor and thus may have oncogenic activity

The "RUNDC1 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 RUNDC1 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

RUNDC3A | RUNDC3A-AS1 | RUNDC3B | RUNX1 | RUNX1-IT1 | RUNX1T1 | RUNX2 | RUNX2-AS1 | RUNX3 | RUNX3-AS1 | RUSC1 | RUSC1-AS1 | RUSC2 | RUSF1 | RUVBL1 | RUVBL1-AS1 | RUVBL2 | RWDD1 | RWDD2A | RWDD2B | RWDD3 | RWDD3-DT | RWDD4 | RXFP1 | RXFP2 | RXFP3 | RXFP4 | RXRA | RXRB | RXRG | RXYLT1 | Ryanodine receptor | RYBP | RYK | RYR1 | RYR2 | RYR3 | RZZ complex | S100 Calcium Binding Protein | S100A1 | S100A10 | S100A11 | S100A11P1 | S100A12 | S100A13 | S100A14 | S100A16 | S100A2 | S100A3 | S100A4 | S100A5 | S100A6 | S100A7 | S100A7A | S100A7L2 | S100A7P1 | S100A8 | S100A9 | S100B | S100G | S100P | S100PBP | S100Z | S1PR1 | S1PR1-DT | S1PR2 | S1PR3 | S1PR4 | S1PR5 | SAA1 | SAA2 | SAA2-SAA4 | SAA3P | SAA4 | SAAL1 | SAC3D1 | SACM1L | SACS | SACS-AS1 | SAE1 | SAFB | SAFB2 | SAG | SAGA complex | SAGE1 | SALL1 | SALL2 | SALL3 | SALL4 | SALL4P7 | SALRNA2 | SAMD1 | SAMD10 | SAMD11 | SAMD12 | SAMD12-AS1 | SAMD13 | SAMD14 | SAMD15 | SAMD3