Target Name: HNRNPA1P60
NCBI ID: G120364
Review Report on HNRNPA1P60 Target / Biomarker Content of Review Report on HNRNPA1P60 Target / Biomarker
HNRNPA1P60
Other Name(s): Heterogeneous nuclear ribonucleoprotein A1 pseudogene 60 | heterogeneous nuclear ribonucleoprotein A1 pseudogene 60

HNRNPA1P60: A Potential Drug Target and Biomarker

Hepatitis B virus (HBV) is a highly infectious and potentially fatal disease that affects millions of people worldwide. The virus causes progressive liver damage and can lead to various health complications, including liver cancer. Currently, there is no cure for HBV, and many patients are treated with nucleotide analog inhibitors (NAs), which can cause serious side effects. As such, there is a growing interest in identifying new drug targets and biomarkers for HBV treatment.

One potential drug target and biomarker that has received attention in recent years is HNRNPA1P60, a non-coding RNA molecule that has been identified in the hepatocellular carcinoma (HCC) cell line as a potential drug target. HNRNPA1P60 has been shown to be highly expressed in HCC tissues and is downregulated in HCC patient samples compared to control tissues. Additionally, overexpression of HNRNPA1P60 has been shown to promote the growth and metastasis of HCC tumors.

The potential drug target for HNRNPA1P60 is its role in cell signaling pathways, particularly the Wnt/FGF signaling pathway. This pathway is involved in cell growth, differentiation, and angiogenesis, and has been implicated in the development and progression of many diseases, including HCC.

HNRNPA1P60 has been shown to be involved in the regulation of Wnt/FGF signaling in several ways. Firstly, HNRNPA1P60 has been shown to be a negative regulator of the Wnt/FGF signaling pathway, specifically of the FGF1 signaling pathway. This means that when FGF1 is activated, HNRNPA1P60 is able to inhibit its effects, preventing the cell from undergoing FGF-mediated signaling.

Secondly, HNRNPA1P60 has been shown to be involved in the regulation of the Wnt/FGF signaling pathway in a positive sense. This means that when FGF1 is inhibited, HNRNPA1P60 is able to increase its effects, leading to the activation and proliferation of the cells.

Finally, HNRNPA1P60 has been shown to be involved in the regulation of the Wnt/FGF signaling pathway in a negative sense. This means that when FGF1 is activated, HNRNPA1P60 is able to inhibit its effects, preventing the cell from undergoing FGF-mediated signaling.

The potential drug target for HNRNPA1P60 is its role in cell signaling pathways, particularly the Wnt/FGF signaling pathway. This pathway is involved in cell growth, differentiation, and angiogenesis, and has been implicated in the development and progression of many diseases, including HCC.

In conclusion, HNRNPA1P60 is a promising drug target and biomarker for the treatment of HCC. The regulation of Wnt/FGF signaling by HNRNPA1P60 makes it a potential target for small molecules that can inhibit its effects. Further studies are needed to confirm its potential as a drug target and to develop new biomarkers for the diagnosis and treatment of HCC.

Protein Name: Heterogeneous Nuclear Ribonucleoprotein A1 Pseudogene 60

The "HNRNPA1P60 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 HNRNPA1P60 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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