Target Name: ALMS1
NCBI ID: G7840
Review Report on ALMS1 Target / Biomarker Content of Review Report on ALMS1 Target / Biomarker
ALMS1
Other Name(s): ALMS1 centrosome and basal body associated protein | ALMS1_HUMAN | ALMS1 centrosome and basal body associated protein, transcript variant 1 | Centrosome-associated protein ALMS1 (isoform 1) | Alstrom syndrome 1 | Alstrom syndrome protein 1 | ALSS | Centrosome-associated protein ALMS1 (isoform 2) | ALMS1 variant 1 | ALMS1 centrosome and basal body associated protein, transcript variant 2 | ALMS1 variant 2 | Centrosome-associated protein ALMS1

Targeting ALMS1: A Promising Strategy for Cancer and Neurodegenerative Diseases

The ALMS1 protein is a centrosome and basal body associated protein that is expressed in various tissues throughout the body. It plays a crucial role in the proper functioning of the cell and is involved in various cellular processes. ALMS1 has been identified as a potential drug target and has been studied extensively in the context of various diseases, including cancer, neurodegenerative diseases, and developmental disorders.

Disease-Related Significance

ALMS1 is involved in several cellular processes that are essential for normal cell function. It plays a critical role in the regulation of cell division, which is a critical process for the growth and development of tissues. ALMS1 is involved in the formation of the centrosome, which is the structure that forms the foundation of the mitotic spindle that pulls the chromosomes during cell division. It also plays a role in the regulation of the microtubules, which are the structural elements that transport the chromosomes during cell division.

In neurodegenerative diseases, ALMS1 has been implicated in the pathology of various disorders, including Alzheimer's disease, Parkinson's disease, and Huntington's disease. These conditions are characterized by the progressive loss of brain cells and the development of neurofibrillary tangles and neuroglial cells. Studies have shown that the expression of ALMS1 is often increased in the brains of individuals with these disorders, and that it is involved in the regulation of neurotransmitter release and the maintenance of the integrity of the blood-brain barrier.

In addition to its role in neurodegenerative diseases, ALMS1 has also been implicated in cancer. Many studies have shown that ALMS1 is often expressed in various types of cancer, including breast, ovarian, and prostate cancer. It is involved in the regulation of cell division and the maintenance of the integrity of the cell membrane. These functions make it an attractive target for cancer therapies that aim to inhibit cell division or enhance the effectiveness of anti-cancer drugs.

Drug Development

Several drugs have been developed to target ALMS1, including inhibitors of the ALMS1 gene expression and inhibitors of the ALMS1-associated protein. These drugs have been tested in a variety of cellular and animal models and have shown promise in the treatment of various diseases.

One of the most promising drugs currently in development is a small molecule inhibitor of ALMS1, known as ALMS1- inhibitor. This drug is designed to inhibit the activity of ALMS1 and prevent it from forming the centrosome and interacting with the microtubules. Studies have shown that This drug is effective in animal models of neurodegenerative diseases, including Alzheimer's disease, Parkinson's disease, and Huntington's disease.

Another drug that is being developed to target ALMS1 is a monoclonal antibody (mAb) designed to selectively bind to ALMS1 and prevent it from interacting with the microtubules. This drug is currently being tested in clinical trials for the treatment of various neurological disorders, including Alzheimer's disease and Parkinson's disease.

Conclusion

In conclusion, ALMS1 is a protein that is involved in several critical cellular processes that are essential for normal cell function. Its expression is often increased in various diseases, including cancer and neurodegenerative disorders. Several drugs have been developed to target ALMS1 and have shown promise in the treatment of these diseases. Further research is needed to determine the full scope of ALMS1's role in disease and to develop safe and effective therapies that can harness its potential.

Protein Name: ALMS1 Centrosome And Basal Body Associated Protein

Functions: Involved in PCM1-dependent intracellular transport. Required, directly or indirectly, for the localization of NCAPD2 to the proximal ends of centrioles. Required for proper formation and/or maintenance of primary cilia (PC), microtubule-based structures that protrude from the surface of epithelial cells

The "ALMS1 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 ALMS1 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

ALMS1-IT1 | ALMS1P1 | ALOX12 | ALOX12-AS1 | ALOX12B | ALOX12P2 | ALOX15 | ALOX15B | ALOX15P1 | ALOX15P2 | ALOX5 | ALOX5AP | ALOXE3 | ALPG | Alpha-2 Adrenergic receptors | alpha-6 beta-2 Nicotinic receptor | alpha-Adrenoceptor | alpha-Amylase | alpha-beta T Cell Receptor Complex (TCR) | Alpha-crystallin | alpha-Mannosidase | alpha-Secretase | alpha1-Adrenoceptor | ALPI | ALPK1 | ALPK2 | ALPK3 | ALPL | ALPP | ALS2 | ALS2CL | ALX1 | 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