Target Name: QSOX1
NCBI ID: G5768
Review Report on QSOX1 Target / Biomarker Content of Review Report on QSOX1 Target / Biomarker
QSOX1
Other Name(s): FLJ34858 | quiescin sulfhydryl oxidase 1 | thiol oxidase 1 | Sulfhydryl oxidase 1 (isoform a) | Quiescin Q6 sulfhydryl oxidase 1 | OTTHUMP00000033189 | Quiescin Q6 | Quiescin sulfhydryl oxidase 1, transcript variant 2 | QSOX1 variant 2 | OTTHUMP00000039111 | Sulfhydryl oxidase 1 | hQSOX | Sulfhydryl oxidase 1 (isoform b) | testis tissue sperm-binding protein Li 62n | quiescin Q6 sulfhydryl oxidase 1 | Thiol:oxygen oxidoreductase | QSCN6 | QSOX1 variant 1 | QSOX1_HUMAN | Thiol oxidase 1 (isoform a) | Q6 | Quiescin sulfhydryl oxidase 1, transcript variant 1

QSOX1: A Potential Drug Target and Biomarker for ALZHEIMER'S DISEASE

Introduction

Alzheimer's disease is a progressive neurological disorder that affects millions of people worldwide, leading to cognitive decline, memory loss, and other debilitating symptoms. Currently, there is no cure for Alzheimer's disease, and numerous treatments are either ineffective or carry significant side effects. Therefore , the development of new treatments and potential drug targets is of great importance. One potential drug target and biomarker for Alzheimer's disease is QSOX1 (FLJ34858), a gene that has not yet been fully studied but is known to be involved in several cellular processes involved in the development and progression of Alzheimer's disease.

QSOX1: A Potential Drug Target

QSOX1 is a gene that encodes a protein known as QSOX1, which is a key regulator of the microtubule network. The microtubules are a protein structure that organizes and maintains the integrity of cells, including those involved in the transmission of signals within cells. Alterations in the microtubule network have been implicated in the development and progression of numerous diseases, including Alzheimer's disease.

Studies have shown that QSOX1 is involved in the regulation of several cellular processes that are crucial for the normal functioning of neuronal cells. For example, QSOX1 has been shown to play a role in the regulation of the trafficking of neural granule cells, which are responsible for transmitting signals within neuronal cells. Additionally, QSOX1 has been shown to contribute to the maintenance of the integrity of the blood-brain barrier, which is responsible for protecting the brain from harmful substances and allowing necessary nutrients to enter the brain.

Furthermore, studies have suggested that QSOX1 may be involved in the regulation of neurodegeneration, which is a common feature of Alzheimer's disease. For example, animal models of Alzheimer's disease have shown that QSOX1-deficient mice exhibit signs of neurodegeneration, including the accumulation of neurofibrillary tangles and the reduction in the number of neural granule cells.

In addition to its involvement in neurodegeneration, QSOX1 has also been implicated in the regulation of neuroplasticity, which is the ability of the brain to reorganize itself in response to new experiences or learning. Studies have shown that QSOX1 plays a role in the regulation of neuroplasticity , and that it is involved in the formation of new neural connections in the brain.

QSOX1 as a Potential Biomarker

The lack of effective treatments for Alzheimer's disease has led to the search for new biomarkers that can be used to diagnose and treat the disease. QSOX1 is an attractive biomarker for Alzheimer's disease because it is involved in several cellular processes that are involved in the development and progression of the disease.

One of the key advantages of QSOX1 as a biomarker is its potential to be used as a diagnostic tool. The QSOX1 gene has not yet been extensively studied, but studies have shown that it is expressed in the brains of individuals with Alzheimer's disease. Additionally, because QSOX1 is involved in the regulation of several cellular processes, changes in its expression levels may indicate the presence of neurodegeneration or neuroplasticity. This could make QSOX1 an effective diagnostic tool for Alzheimer's disease.

Another advantage of QSOX1 as a biomarker is its potential to be used as a target for new treatments. The microtubule network plays a crucial role in the regulation of cellular processes, and alterations in

Protein Name: Quiescin Sulfhydryl Oxidase 1

Functions: Catalyzes the oxidation of sulfhydryl groups in peptide and protein thiols to disulfides with the reduction of oxygen to hydrogen peroxide (PubMed:17331072, PubMed:18393449, PubMed:23704371, PubMed:30367560, PubMed:23867277). Plays a role in disulfide bond formation in a variety of extracellular proteins (PubMed:17331072, PubMed:30367560, PubMed:22801504, PubMed:23867277). In fibroblasts, required for normal incorporation of laminin into the extracellular matrix, and thereby for normal cell-cell adhesion and cell migration (PubMed:23704371, PubMed:30367560, PubMed:23867277)

The "QSOX1 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 QSOX1 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

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QSOX2 | QTRT1 | QTRT2 | Queuine tRNA-ribosyltransferase | R-Spondin | R3HCC1 | R3HCC1L | R3HDM1 | R3HDM2 | R3HDM4 | R3HDML | R3HDML-AS1 | RAB GTPase | RAB10 | RAB11A | RAB11AP2 | RAB11B | RAB11B-AS1 | RAB11FIP1 | RAB11FIP2 | RAB11FIP3 | RAB11FIP4 | RAB11FIP5 | RAB12 | RAB13 | RAB14 | RAB15 | RAB17 | RAB18 | RAB19 | RAB1A | RAB1B | RAB20 | RAB21 | RAB22A | RAB23 | RAB24 | RAB25 | RAB26 | RAB27A | RAB27B | RAB28 | RAB29 | RAB2A | RAB2B | RAB3 GTPase activating protein | RAB30 | RAB30-DT | RAB31 | RAB32 | RAB33A | RAB33B | RAB34 | RAB35 | RAB36 | RAB37 | RAB38 | RAB39A | RAB39B | RAB3A | RAB3B | RAB3C | RAB3D | RAB3GAP1 | RAB3GAP2 | RAB3IL1 | RAB3IP | RAB40A | RAB40AL | RAB40B | RAB40C | RAB41 | RAB42 | RAB42P1 | RAB43 | RAB43P1 | RAB44 | RAB4A | RAB4B | RAB4B-EGLN2 | RAB5A | RAB5B | RAB5C | RAB5IF | RAB6A | RAB6B | RAB6C | RAB6C-AS1 | RAB6D | RAB7A | RAB7B | RAB8A | RAB8B | RAB9A | RAB9B | RAB9BP1 | RABAC1 | RABEP1 | RABEP2 | RABEPK