Target Name: ALX1
NCBI ID: G8092
Review Report on ALX1 Target / Biomarker Content of Review Report on ALX1 Target / Biomarker
ALX1
Other Name(s): Cartilage paired-class homeoprotein 1 | Cartilage homeoprotein 1 | ALX1_HUMAN | ALX homeobox 1 | CART1 | cartilage paired-class homeoprotein 1 | FND3 | epididymis luminal protein 23 | HEL23 | ALX homeobox protein 1 | CART-1

ALX1: A Potential Drug Target and Biomarker for Cartilage-Paired-Class Homeoprotein 1

Cartilage-paired-class homeoprotein (ALX1) is a protein that is expressed in human articular cartilage, which is the tissue that supports and protects the joints. It plays a crucial role in maintaining the mechanical stability of the joint and is involved in various physiological processes, including pain signaling and tissue repair. The discovery of ALX1 as a potential drug target and biomarker has significant implications for the treatment of joint disorders and degenerative diseases.

ALX1: A Key Protein in Articular Tissue

The ALX1 gene is located on chromosome 16 and encodes a 16-kDa protein that is expressed in articular cartilage. It is one of the major proteins involved in the structure and function of articular cartilage and is responsible for maintaining its mechanical stability. ALX1 is highly conserved across different species, which indicates that it has a critical role in the development and maintenance of articular tissue.

During the development of an articular joint, ALX1 plays a crucial role in the formation of the hyaline cartilage. Hyaline cartilage is the outermost layer of articular cartilage and is responsible for providing a supportive and durable structure for the joint. The ALX1 gene is expressed during the entire development of the hyaline cartilage and is involved in the formation of the collagen fibers that make up the hyaline cartilage.

ALX1: A Potential Drug Target

The discovery of ALX1 as a potential drug target has significant implications for the treatment of joint disorders and degenerative diseases. ALX1 is involved in various physiological processes in articular tissue, including pain signaling and tissue repair. Therefore, inhibiting the activity of ALX1 may offer a new approach to treating joint disorders and degenerative diseases.

One of the potential mechanisms by which ALX1 may contribute to joint disorders is its role in pain signaling. Articular pain is often associated with inflammation and the production of pro-inflammatory cytokines, which can activate pain receptors and contribute to the development of pain. ALX1 has been shown to be involved in the production of pro-inflammatory cytokines, including TNF-alpha, IL-1, and IL-6. By inhibiting the activity of ALX1, it may be possible to reduce the production of pro-inflammatory cytokines and alleviate pain.

Another potential mechanism by which ALX1 may contribute to joint disorders is its role in tissue repair. Articular tissue repair is a critical process that occurs in response to injury or degenerative diseases, and is characterized by the production of pro-inflammatory cytokines and the recruitment of immune cells to the site of injury. ALX1 has been shown to be involved in the production of pro-inflammatory cytokines and the recruitment of immune cells to the site of injury. By inhibiting the activity of ALX1, it may be possible to reduce the production of pro-inflammatory cytokines and the recruitment of immune cells, which could potentially improve tissue repair and reduce the risk of joint disorders.

ALX1: A Potential Biomarker

The ALX1 gene has also been shown to be involved in the regulation of inflammation and immune cell function. By analyzing the expression of ALX1 in articular tissue, researchers have found that ALX1 is involved in the production of pro-inflammatory cytokines, including TNF-alpha, IL-1, and IL-6. This suggests that ALX1 may be a potential biomarker for joint inflammation and immune cell function.

In addition to its potential role as a drug target and biomarker, ALX1 is also of interest as a potential therapeutic agent for the treatment of joint disorders and degenerative diseases. The inhibition of ALX1 activity has been shown to reduce the production of pro-inflammatory cytokines and improve tissue repair in experimental models of joint inflammation and degenerative diseases, including rheumatoid arthritis and osteoarthritis. Therefore, ALX1 may be an attractive candidate

Protein Name: ALX Homeobox 1

Functions: Sequence-specific DNA-binding transcription factor that binds palindromic sequences within promoters and may activate or repress the transcription of a subset of genes (PubMed:9753625, PubMed:8756334). Most probably regulates the expression of genes involved in the development of mesenchyme-derived craniofacial structures. Early on in development, it plays a role in forebrain mesenchyme survival (PubMed:20451171). May also induce epithelial to mesenchymal transition (EMT) through the expression of SNAI1 (PubMed:23288509)

The "ALX1 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 ALX1 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

ALX3 | ALX4 | ALYREF | AMACR | AMBN | AMBP | AMBRA1 | AMD1 | AMD1P2 | AMDHD1 | AMDHD2 | AMELX | AMELY | AMER1 | AMER2 | AMER3 | AMFR | AMH | AMHR2 | AMIGO1 | AMIGO2 | AMIGO3 | Amine oxidase (copper containing) | Amino acid hydroxylase | Aminoacyl-tRNA Synthetase Complex | AMMECR1 | AMMECR1L | AMN | AMN1 | AMOT | AMOTL1 | AMOTL2 | AMP Deaminase | AMP-activated protein kinase (AMPK) | AMP-activated protein kinase alpha1beta1gamma1 | AMP-activated protein kinase alpha2beta1gamma1 | AMP-activated protein kinase alpha2beta1gamma2 | AMP-activated protein kinase alpha2beta2gamma2 | AMPD1 | AMPD2 | AMPD3 | AMPH | AMT | AMTN | AMY1A | AMY1B | AMY1C | AMY2A | AMY2B | Amylin receptor | Amyloid beta A4 precursor protein-binding family (APP-BP) | AMZ1 | AMZ2 | AMZ2P1 | Anandamide membrane transporter (AMT) | ANAPC1 | ANAPC10 | ANAPC10P1 | ANAPC11 | ANAPC13 | ANAPC15 | ANAPC16 | ANAPC1P1 | ANAPC1P2 | ANAPC2 | ANAPC4 | ANAPC5 | ANAPC7 | ANG | ANGEL1 | ANGEL2 | Angiogenic Factor | Angiotensin receptor (AT) | ANGPT1 | ANGPT2 | ANGPT4 | ANGPTL1 | ANGPTL2 | ANGPTL3 | ANGPTL4 | ANGPTL5 | ANGPTL6 | ANGPTL7 | ANGPTL8 | ANHX | ANK1 | ANK2 | ANK3 | ANKAR | ANKDD1A | ANKDD1B | ANKEF1 | ANKFN1 | ANKFY1 | ANKH | ANKHD1 | ANKHD1-EIF4EBP3 | ANKIB1 | ANKK1 | ANKLE1