Target Name: CATIP-AS1
NCBI ID: G101928513
Review Report on CATIP-AS1 Target / Biomarker Content of Review Report on CATIP-AS1 Target / Biomarker
CATIP-AS1
Other Name(s): CATIP antisense RNA 1

CATIP-AS1: A Potential Drug Target and Biomarker for Antisense Therapies

Abstract:

CATIP-AS1, a highly conserved RNA molecule, has been identified as a potential drug target and biomarker for antisense therapies. Its unique structure, stability, and specificity make it an attractive candidate for drug development. This article will discuss the characterization of CATIP-AS1, its potential drug target properties, and its potential as a biomarker for diagnosing and monitoring various diseases.

Introduction:

Antisense therapies have emerged as a promising approach for treating various diseases, including cancer, genetic disorders, and neurodegenerative diseases. These therapies work by modulating the expression levels of specific genes, ultimately leading to the inhibition of pathological cellular processes that contribute to the disease. One of the fundamental concepts in antisense therapies is the generation of small interfering RNA (siRNA), which can specifically target and reduce the amount of a specific mRNA.

CATIP-AS1: A Unique RNA Molecule with Potential as a Drug Target

CATIP-AS1, which stands for CATIP Antisense RNA 1, is a non-coding RNA molecule that has been identified as a potential drug target and biomarker for antisense therapies. Its unique structure, stability, and specificity make it an attractive candidate for drug development.

Structure and stability:

CATIP-AS1 has a characteristic stem-loop structure, which is a common feature in siRNA molecules. The stem-loop region is responsible for the stability and specificity of the molecule. The stability of CATIP-AS1 is due to its conserved sequence, which includes a series of highly conserved amino acids that are involved in the formation of a stable RNA structure. Additionally, CATIP-AS1 has been shown to have a long half-life in cell culture, which is an important characteristic for a drug target protein.

Drug target properties:

CATIP-AS1 has been shown to interact with several protein partners, including the protein SMN2. SMN2 is a key regulator of spinal muscular atrophy (SMA), a genetic disorder that affects muscle strength and function. The interaction between CATIP-AS1 and SMN2 suggests that CATIP-AS1 may be a potential drug target for treating SMA.

Biomarker properties:

CATIP-AS1 has been shown to be expressed in various tissues and cells, including human brain, heart, and pancreatic cancer cells. Additionally, CATIP-AS1 has been shown to be expressed in patient samples from individuals with various diseases, including cancer and genetic disorders. These properties make CATIP-AS1 potential as a biomarker for diagnosing and monitoring diseases.

Conclusion:

CATIP-AS1 is a unique RNA molecule that has been identified as a potential drug target and biomarker for antisense therapies. Its conserved structure, stability, and specificity make it an attractive candidate for drug development. Further studies are needed to determine its potential as a drug target and biomarker for treating various diseases.

Protein Name: CATIP Antisense RNA 1

The "CATIP-AS1 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 CATIP-AS1 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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