Target Name: CDON
NCBI ID: G50937
Review Report on CDON Target / Biomarker Content of Review Report on CDON Target / Biomarker
CDON
Other Name(s): CDON variant 2 | Cell adhesion associated, oncogene regulated, transcript variant 2 | CDON_HUMAN | ORCAM | CDON variant 1 | surface glycoprotein, Ig superfamily member | Cell adhesion molecule-related/down-regulated by oncogenes (isoform 2) | Cdon homolog | CDON1 | Cell adhesion molecule-related/down-regulated by oncogenes (isoform 1) | cell adhesion associated, oncogene regulated | Surface glycoprotein, Ig superfamily member | Ihog | Cell adhesion molecule-related/down-regulated by oncogenes | MGC111524 | Cell adhesion molecule-related/down-regulated by oncogenes [Precursor] | Cell adhesion associated, oncogene regulated, transcript variant 1 | HPE11 | CDO

CDON Variant 2: A Potential Drug Target and Biomarker

CDON (CDON variant 2) is a non-coding RNA molecule that has been identified as a potential drug target and biomarker. CDON is a key regulator of gene expression in various cell types, including cancer cells. The variants of CDON have been observed in various diseases, including cancer, neurodegenerative diseases, and systemic diseases. This article will discuss the CDON variant 2, its potential as a drug target, and its potential as a biomarker.

Potential Drug Target

CDON variant 2 has been shown to play a critical role in the regulation of cell proliferation and apoptosis. It has been shown to inhibit the activity of the oncogene transforming growth factor-尾 (TGF-β), which is a key regulator of cell proliferation. In addition, CDON variant 2 has been shown to promote the apoptosis of cancer cells, which is a key mechanism in the development of cancer.

The potential drug target for CDON variant 2 is the inhibition of TGF-β signaling pathway. This can be achieved by targeting the protein SMAD (small molecule-activated nuclear factor of DNA binding) which is a negative regulator of TGF-β. By inhibiting the activity of SMAD, CDON variant 2 can lead to the activation of TGF-β, thereby inhibiting its ability to promote cell proliferation and apoptosis.

Potential Biomarker

CDON variant 2 has also been shown to serve as a potential biomarker for various diseases, including cancer. The expression of CDON variant 2 has been shown to be significantly higher in cancer cells compared to healthy tissue. This increased expression of CDON variant 2 can be used as a biomarker for the detection and diagnosis of cancer.

In addition, the expression of CDON variant 2 has also been shown to be associated with the poor prognosis of cancer patients. This suggests that the level of CDON variant 2 expression may be a useful biomarker for the prediction of cancer outcomes.

Conclusion

CDON variant 2 has been shown to be a potential drug target and biomarker in various diseases. The inhibition of TGF-β signaling pathway by CDON variant 2 has the potential to be a useful therapy for the treatment of cancer. The potential biomarker properties of CDON variant 2 make it an attractive target for the development of diagnostic tests for cancer. Further research is needed to fully understand the role of CDON variant 2 as a drug target and biomarker.

Protein Name: Cell Adhesion Associated, Oncogene Regulated

Functions: Component of a cell-surface receptor complex that mediates cell-cell interactions between muscle precursor cells. Promotes differentiation of myogenic cells (By similarity)

The "CDON 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 CDON 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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