Target Name: HHIPL2
NCBI ID: G79802
Review Report on HHIPL2 Target / Biomarker Content of Review Report on HHIPL2 Target / Biomarker
HHIPL2
Other Name(s): FLJ13840 | Hedgehog interacting protein-like 2 | RP11-378J18.1 | HHIP like 2 | HIPL2_HUMAN | HHIP-like protein 2 | hedgehog interacting protein-like 2 | KIAA1822L

HHIPL2: A Potential Drug Target for HBsAg-Positive Individuals

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 cirrhosis, cancer, and death. Currently, there is no cure for HBV, and treatments are often limited to managing symptoms and preventing complications. The hepatitis B surface antigen (HBsAg) is a viral envelope protein that is present in the majority of HBV-infected individuals and has been identified as a potential drug target in the treatment of HBV-related diseases. One of the potential drug targets for HBsAg is the heparin-like peptide-2 (HPP2), which is a type of extracellular matrix (ECM) protein that is derived from the plasma of animals, including humans. In this article, we will discuss the HHIPL2 protein, which is a potential drug target for HBsAg, and its potential as a therapeutic agent in the treatment of HBV-related diseases.

Hepatitis B virus and its impact on public health

HBV is a member of the family Herpesviridae, which includes other viruses such as herpes simplex virus (HSV) and varicella-zoster virus (VZV). HBV is the most common cause of liver damage and cirrhosis in the world, with over 1.4 million people affected worldwide. The virus is transmitted through contact with contaminated blood or other bodily fluids, such as semen, vaginal fluids, and urine. It is also possible to transmit the virus through the use of shared needles or the sharing of personal care products such as razors or toothbrushes.

HBV can cause a range of symptoms, including mild to severe fatigue, loss of appetite, nausea and vomiting, abdominal pain and discomfort, dark urine, and yellowing of the skin and eyes (jaundice). Over time, the virus can cause more serious health complications, such as liver cirrhosis, liver cancer, and death. According to the World Health Organization (WHO), over 30% of people with HBV will develop cirrhosis, which can lead to symptoms such as abdominal pain and jaundice, and increases the risk of liver failure and death.

Current treatments for HBV

Current treatments for HBV are limited to managing symptoms and preventing complications. The most common treatment for HBV is a course of antiviral medications, which can help reduce the level of the virus in the body and reduce the severity of any symptoms. These medications can also help prevent the development of cirrhosis and other serious health complications.

Antiviral medications can be divided into two categories: nucleotide analog inhibitors and non-nucleotide analog inhibitors. Nucleotide analog inhibitors, such as tenofovir (LdT) and entecavir (ETV), are commonly used to treat HBsAg positive individuals. They work by inhibiting the viral replication of the virus, which can reduce the level of the virus in the body. Non-nucleotide analog inhibitors, such as telbivudine (LdT) and telgevudine (LdA), are also used to treat HBsAg positive individuals. They work by inhibiting the viral replication of the virus, which can reduce the level of the virus in the body.

HHIPL2 as a potential drug target

HHIPL2 is a type of ECM protein that is derived from the plasma of animals, including humans. It is expressed in various tissues and cells of the body, including the liver, and has been shown to play a role in the immune response and the regulation of inflammation. HHIPL2 has also been shown to have anti-inflammatory properties and to be expressed in the liver tissue of HBsAg-positive individuals.

In addition, HHIPL2 has been shown to interact with the viral envelope protein HBsAg, which is a key component of the virus that allows it to infect host cells. Studies have shown that HHIPL2 can bind to HBsAg and can inhibit the viral replication of the virus . This suggests that HHIPL2 may be a potential drug target for HBsAg-positive individuals.

Potential therapeutic applications of HHIPL2

The potential therapeutic applications of HHIPL2 are vast. As a drug target

Protein Name: HHIP Like 2

The "HHIPL2 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 HHIPL2 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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HHLA1 | HHLA2 | HHLA3 | HIBADH | HIBCH | HIC1 | HIC2 | HID1 | HID1-AS1 | HIF1A | HIF1A-AS1 | HIF1A-AS2 | HIF1A-AS3 | HIF1AN | HIF3A | HIGD1A | HIGD1AP1 | HIGD1AP10 | HIGD1B | HIGD1C | HIGD2A | HIGD2B | High affinity cAMP-specif | High Affinity Immunoglobulin Epsilon Fc Receptor | HIKESHI | HILPDA | HILPDA-AS1 | HINFP | HINT1 | HINT1P1 | HINT2 | HINT3 | HIP1 | HIP1R | HIPK1 | HIPK1-AS1 | HIPK2 | HIPK3 | HIPK4 | HIRA | HIRIP3 | HISLA | Histamine Receptor (HR) | Histocompatibility antigen-related | Histone | Histone acetyltransferase (HAT) | Histone deacetylase | Histone H2A | Histone H2B | Histone H3 | Histone Lysine Demethylase | Histone methyltransferase | HIVEP1 | HIVEP2 | HIVEP3 | HJURP | HJV | HK1 | HK2 | HK2P1 | HK3 | HKDC1 | HLA Class II Histocompatibility Antigen DM (HLA-DM) | HLA class II histocompatibility Antigen DO (HLA-DO) | HLA class II histocompatibility antigen DP (HLA-DP) | HLA Class II Histocompatibility Antigen DQ8 | HLA class II histocompatibility antigen DR (HLA-DR) | HLA Class II Histocompatibility Antigen, DQ (HLA-DQ) | HLA class II histocompatibility antigen, DRB1-7 beta chain, transcript variant X1 | HLA complex group 16 (non-protein coding), transcript variant X2 | HLA complex group 8 | HLA-A | HLA-B | HLA-C | HLA-DMA | HLA-DMB | HLA-DOA | HLA-DOB | HLA-DPA1 | HLA-DPA2 | HLA-DPA3 | HLA-DPB1 | HLA-DPB2 | HLA-DQA1 | HLA-DQA2 | HLA-DQB1 | HLA-DQB1-AS1 | HLA-DQB2 | HLA-DRA | HLA-DRB1 | HLA-DRB2 | HLA-DRB3 | HLA-DRB4 | HLA-DRB5 | HLA-DRB6 | HLA-DRB7 | HLA-DRB8 | HLA-DRB9 | HLA-E | HLA-F