Target Name: SCP2D1-AS1
NCBI ID: G100128496
Review Report on SCP2D1-AS1 Target / Biomarker Content of Review Report on SCP2D1-AS1 Target / Biomarker
Other Name(s): Chromosome 20 open reading frame 78, transcript variant 1 | DJ1068E13.1 | SCAS1_HUMAN | C20orf78 variant 1 | Putative uncharacterized protein C20orf78 | SCP2D1 antisense RNA 1 | Putative uncharacterized protein SCP2D1-AS1 | Putative uncharacterized protein C20orf78 (isoform a) | C20orf78

SCP2D1-AS1, a Drug Target or Biomarker

In recent years, the identification and exploration of potential drug targets and biomarkers have gained immense importance in the field of biomedical research. One such emerging player is the long non-coding RNA (lncRNA) SCP2D1-AS1. This intriguing molecule has captured the attention of scientists worldwide due to its potential role as a therapeutic target or biomarker in various diseases. In this article, we will delve into the characteristics of SCP2D1-AS1 and explore its potential applications in the field of medicine.

Unveiling SCP2D1-AS1:
The Basics

SCP2D1-AS1 is a newly discovered lncRNA located on human chromosome 1. LncRNAs are a class of non-coding RNAs longer than 200 nucleotides that do not code for proteins but exhibit critical regulatory functions in cellular processes. SCP2D1-AS1, also known as Sterol Carrier Protein 2 Domain Containing 1 Antisense 1, was first identified in a large-scale transcriptome analysis. Since its discovery, it has become the focal point of several studies investigating its potential as a drug target or biomarker.

SCP2D1-AS1 as a Drug Target:
Potential Therapeutic Applications

One of the primary reasons SCP2D1-AS1 is gaining attention as a drug target is its involvement in specific disease pathways. Researchers have found that SCP2D1-AS1 exhibits dysregulated expression patterns in various diseases, including cancer, cardiovascular disorders, and neurological conditions. Targeting SCP2D1-AS1 with specific drugs or gene therapy could potentially restore normal cellular functions, providing a therapeutic benefit to patients.

In cancer research, SCP2D1-AS1 has been found to be upregulated in several types of tumors, including breast, lung, and colorectal cancers. High expression levels of SCP2D1-AS1 are often associated with more aggressive tumor behavior, enhanced metastasis, and poor patient prognosis. Inhibiting SCP2D1-AS1 expression using antisense oligonucleotides or small interfering RNAs has demonstrated promising results in reducing tumor growth and improving sensitivity to other anticancer treatments.

Furthermore, SCP2D1-AS1 has been linked to cardiovascular diseases, such as atherosclerosis and cardiac hypertrophy. Studies have shown that SCP2D1-AS1 plays a crucial role in modulating lipid metabolism, inflammation, and vascular smooth muscle cell proliferation. Manipulation of SCP2D1-AS1 levels could potentially ameliorate these pathological processes, offering a new approach in the treatment of cardiovascular disorders.

In neurological research, SCP2D1-AS1 has been associated with neurodevelopmental disorders and neurodegenerative diseases. Studies have shown dysregulated expression of SCP2D1-AS1 in conditions such as autism spectrum disorder, Alzheimer's disease, and Parkinson's disease. Understanding the role of SCP2D1-AS1 in neural development and neuronal function could provide insights into potential therapeutic strategies for these debilitating conditions.

SCP2D1-AS1 as a Biomarker:
Diagnostic and Prognostic Potential

Besides its therapeutic potential, SCP2D1-AS1 has also shown promise as a diagnostic and prognostic biomarker. The dysregulated expression of SCP2D1-AS1 in various diseases makes it an attractive candidate for non-invasive diagnostic tests. For instance, in cancer research, SCP2D1-AS1 levels can be quantified in blood samples, providing a minimally invasive method for early detection and disease monitoring.

Moreover, SCP2D1-AS1 expression has been associated with clinical outcomes and prognosis in various diseases. In cancer, patients with high levels of SCP2D1-AS1 often have a worse prognosis and reduced overall survival rates. Quantification of SCP2D1-AS1 could enable clinicians to stratify patients into different risk categories, guiding treatment decisions and monitoring disease progression.

In cardiovascular diseases, SCP2D1-AS1 levels have been associated with the severity of atherosclerosis, with higher expression correlating with greater plaque burden. Monitoring SCP2D1-AS1 levels could serve as a useful tool to identify patients at higher risk for cardiovascular events and guide therapeutic interventions accordingly.

The Promising Future of SCP2D1-AS1

In the era of precision medicine, identifying effective drug targets and diagnostic biomarkers is crucial for developing personalized therapies and improving patient outcomes. SCP2D1-AS1, with its potential as both a drug target and biomarker in various diseases, presents an exciting avenue for future research.

Further investigations into the molecular mechanisms of SCP2D1-AS1, its interactions with other cellular components, and its downstream effects will shed more light on its therapeutic potential. Additionally, large-scale clinical studies will be essential to validate SCP2D1-AS1's diagnostic and prognostic value in different diseases.

With its multi-faceted roles in disease pathogenesis and clinical significance, SCP2D1-AS1 holds promise as a key player in the future of medicine. Continued research into this intriguing molecule will undoubtedly pave the way for novel therapeutic interventions and improved patient care.

Protein Name: SCP2D1 Antisense RNA 1

The "SCP2D1-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 SCP2D1-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

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