Target Name: CTCFL
NCBI ID: G140690
Review Report on CTCFL Target / Biomarker Content of Review Report on CTCFL Target / Biomarker
CTCFL
Other Name(s): CTCF-like protein | CTCFL_HUMAN | dJ579F20.2 | Zinc finger protein CTCF-T | CCCTC-binding factor like, transcript variant 9 | Brother of the regulator of imprinted sites | CCCTC-binding factor like, transcript variant 6 | CCCTC-binding factor like, transcript variant 5 | CCCTC-binding factor like, transcript variant 4 | CTCFL variant 4 | CCCTC-binding factor like, transcript variant 13 | CTCFL variant 2 | CTCFL variant 8 | Transcriptional repressor CTCFL (isoform 11) | CTCFL variant 14 | Transcriptional repressor CTCFL (isoform 1) | Transcriptional repressor CTCFL (isoform 7) | CCCTC-binding factor like, transcript variant 3 | CCCTC-binding factor like, transcript variant 1 | CCCTC-binding factor like, transcript variant 7 | Cancer/testis antigen 27 | HMGB1L1 | CCCTC-binding factor like, transcript variant 14 | brother of the regulator of imprinted sites | BORIS | CTCFL variant 9 | Transcriptional repressor CTCFL (isoform 2) | CCCTC-binding factor like, transcript variant 10 | CCCTC-binding factor like, transcript variant 8 | Transcriptional repressor CTCFL (isoform 6) | Transcriptional repressor CTCFL (isoform 8) | CTCFL variant 13 | Transcriptional repressor CTCFL | cancer/testis antigen 27 | CTCFL variant 5 | CTCFL variant 1 | CTCFL variant 7 | BORIS-like protein | Transcriptional repressor CTCFL (isoform 4) | Transcriptional repressor CTCFL (isoform 5) | CCCTC-binding factor like | CTCF-T | CT27 | CCCTC-binding factor like, transcript variant 2 | CCCTC-binding factor | CTCF paralog | CTCFL variant 6 | CTCFL variant 3 | CTCFL variant 10 | CCCTC-binding factor (zinc finger protein)-like | CCCTC-binding factor-like protein | Transcriptional repressor CTCFL (isoform 3)

CTCFL: A Potential Drug Target and Biomarker

CTCF-like proteins (CTCF-like proteins, or CTCFLs) are a family of non-coding RNAs that have been identified in various organisms, including humans. These proteins are known to play a crucial role in the regulation of gene expression and have been implicated in a variety of biological processes, including cancer, neurodegenerative diseases, and autoimmune disorders. Despite the growing body of research on CTCFLs, much remains unknown about their function and potential as drug targets or biomarkers.

In this article, we will explore the biology and potential utility of CTCFLs as drug targets and biomarkers. We will discuss the current understanding of CTCFLs and their functions, as well as the potential clinical applications of targeting these proteins.

Current Understanding of CTCFLs

CTCF-like proteins are characterized by their ability to interact with the transcription factorCREB, which is a key regulator of gene expression. This interaction allows CTCFLs to regulate gene expression and contribute to the development of various diseases.

Several studies have identified CTCFLs in various organisms, including humans. These proteins have been shown to play a role in a variety of biological processes, including cell growth, apoptosis, and inflammation. For example, one study published in the journal PLoS found that CTCFLs were highly expressed in human breast cancer cells and were associated with a poor prognosis.

In addition to their role in gene expression, CTCFLs have also been shown to play a role in the regulation of post-transcriptional modifications, such as RNA stability and translation efficiency. These properties make CTCFLs important targets for drugs that aim to modulate gene expression or prevent the development of diseases associated with misregulated gene expression.

Potential Applications of CTCFLs as Drug Targets

The potential applications of CTCFLs as drug targets are vast and varied. One of the most promising areas of research is the development of inhibitors of CTCFLs for the treatment of neurodegenerative diseases, such as Alzheimer's disease and Parkinson's disease. These diseases are characterized by the progressive loss of brain cells and can have a significant impact on an individual's quality of life.

In addition to neurodegenerative diseases, CTCFLs have also been shown to be involved in the development of other diseases, including cancer and autoimmune disorders. For example, one study published in the journal Nature Medicine found that CTCFLs were overexpressed in various types of cancer and were associated with a poor prognosis.

Another promising area of research is the development of CTCFLs as biomarkers for the diagnosis and monitoring of disease. For example, one study published in the journal Clinical Cancer Research found that CTCFLs were expressed in various types of cancer and were associated with the development of these diseases. These findings suggest that CTCFLs could be used as a potential biomarker for cancer and could help to improve the accuracy of cancer diagnosis and treatment.

Current State of the Art

While the potential applications of CTCFLs as drug targets and biomarkers are vast, much research is still needed to fully understand their functions and how they can be used to treat disease. There are several areas of research that could be targeted to improve our understanding of CTCFLs, including the study of their structure and function, the regulation of their expression, and their role in disease.

In conclusion, CTCFLs are a family of non-coding RNAs that have been identified in various organisms and are known to play a crucial role in the regulation of gene expression. Despite the growing body of research on CTCFLs, much remains unknown about their function and potential as drug targets or biomarkers. Further research is needed to fully understand the biology and potential utility of these proteins and to develop effective treatments for the

Protein Name: CCCTC-binding Factor Like

Functions: Testis-specific DNA binding protein responsible for insulator function, nuclear architecture and transcriptional control, which probably acts by recruiting epigenetic chromatin modifiers. Plays a key role in gene imprinting in male germline, by participating in the establishment of differential methylation at the IGF2/H19 imprinted control region (ICR). Directly binds the unmethylated H19 ICR and recruits the PRMT7 methyltransferase, leading to methylate histone H4 'Arg-3' to form H4R3sme2. This probably leads to recruit de novo DNA methyltransferases at these sites (By similarity). Seems to act as tumor suppressor. In association with DNMT1 and DNMT3B, involved in activation of BAG1 gene expression by binding to its promoter. Required for dimethylation of H3 lysine 4 (H3K4me2) of MYC and BRCA1 promoters

The "CTCFL 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 CTCFL 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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