Target Name: HTRA2
NCBI ID: G27429
Other Name(s): HtrA2 | HtrA-like serine protease | HtrA serine peptidase 2 | MGCA8 | protease, serine, 25 | epididymis secretory sperm binding protein | high temperature requirement protein A2 | Protease, serine, 25 | serine protease 25 | HTRA2 variant 1 | HTRA2 variant 2 | Serine protease HTRA2, mitochondrial (isoform 1) | HTRA2_HUMAN | serine proteinase OMI | HtrA serine peptidase 2, transcript variant 2 | Omi stress-regulated endoprotease | OMI | Serine protease HTRA2, mitochondrial (isoform 2) | HtrA serine peptidase 2, transcript variant 1 | Serine protease 25 | Serine protease HTRA2, mitochondrial | High temperature requirement protein A2 | OTTHUMP00000202723 | PARK13 | Serine proteinase OMI | PRSS25

HTRA2: A Potential Drug Target and Biomarker

Heart failure is a condition that affects millions of people worldwide, leading to reduced heart muscle function and increased risk of complications. Currently, there are limited treatment options available for heart failure, and there is a high demand for new therapies that can improve outcomes.

One potential drug target for heart failure is HTRA2, which is a protein that is expressed in the heart muscle. HTRA2 has been shown to play a role in the development and progression of heart failure, and it has been identified as a potential biomarker for the disease.

Research has shown that HTRA2 is involved in various processes that are important for heart function, including contractility, differentiation, and survival. It has been shown to regulate the growth and proliferation of heart muscle cells, and it has been linked to the formation of scar tissue in the heart muscle.

In addition to its role in heart function, HTRA2 has also been shown to play a role in the regulation of inflammation and fibrosis. It has been shown to promote the recruitment of immune cells to the heart muscle, which can lead to inflammation and fibrosis.

Given the potential role of HTRA2 in heart failure, it is an attractive target for new therapies. Researchers have been exploring the use of drugs that can inhibit HTRA2 activity in order to improve heart function and reduce the risk of complications.

One approach to inhibiting HTRA2 activity is through the use of small molecules, such as drugs that can bind to HTRA2 and prevent it from interacting with its downstream targets. This approach has been shown to be effective in animal models of heart failure, and it is now being explored in clinical trials.

Another approach to inhibiting HTRA2 activity is through the use of antibodies, which can target HTRA2 directly and prevent it from interacting with its downstream targets. This approach has been shown to be effective in animal models of heart failure, and it is now being explored in clinical trials.

While HTRA2 is an attractive drug target for heart failure, it is important to note that there are potential risks associated with its use. For example, inhibiting HTRA2 activity can lead to decreased heart function, which can increase the risk of cardiovascular complications.

Additionally, there is the potential for HTRA2 to become resistant to inhibitors, which could limit the effectiveness of these drugs. To address this issue, researchers are exploring the use of combination therapies that can be used to maintain the effectiveness of HTRA2 inhibitors over time.

Overall, HTRA2 is a promising drug target for heart failure, and its potential as a biomarker for the disease is being explored in clinical trials. While it is important to note the potential risks associated with its use, researchers are working to develop new therapies that can improve heart function and reduce the risk of complications in heart failure.

Protein Name: HtrA Serine Peptidase 2

Functions: Serine protease that shows proteolytic activity against a non-specific substrate beta-casein. Promotes or induces cell death either by direct binding to and inhibition of BIRC proteins (also called inhibitor of apoptosis proteins, IAPs), leading to an increase in caspase activity, or by a BIRC inhibition-independent, caspase-independent and serine protease activity-dependent mechanism. Cleaves THAP5 and promotes its degradation during apoptosis. Isoform 2 seems to be proteolytically inactive

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HTRA3 | HTRA4 | HTT | HTT-AS | HULC | Human chorionic gonadotropin | HUNK | HUS1 | HUS1B | HUWE1 | HVCN1 | HYAL1 | HYAL2 | HYAL3 | HYAL4 | HYAL6P | Hyaluronidase | HYCC1 | HYCC2 | HYDIN | HYI | HYKK | HYLS1 | HYMAI | HYOU1 | HYPK | Hypoxia inducible factor (HIF) | Hypoxia-Inducible Factor Prolyl Hydroxylase | I-kappa-B-kinase (IKK) complex | IAH1 | IAPP | IARS1 | IARS2 | IATPR | IBA57 | IBA57-DT | IBSP | IBTK | ICA1 | ICA1L | ICAM1 | ICAM2 | ICAM3 | ICAM4 | ICAM5 | ICE1 | ICE2 | ICMT | ICMT-DT | ICOS | ICOSLG | ID1 | ID2 | ID2-AS1 | ID2B | ID3 | ID4 | IDE | IDH1 | IDH1-AS1 | IDH2 | IDH2-DT | IDH3A | IDH3B | IDH3G | IDI1 | IDI2 | IDI2-AS1 | IDNK | IDO1 | IDO2 | IDS | IDSP1 | IDUA | IER2 | IER3 | IER3-AS1 | IER3IP1 | IER5 | IER5L | IER5L-AS1 | IFFO1 | IFFO2 | IFI16 | IFI27 | IFI27L1 | IFI27L2 | IFI30 | IFI35 | IFI44 | IFI44L | IFI6 | IFIH1 | IFIT1 | IFIT1B | IFIT2 | IFIT3 | IFIT5 | IFITM1 | IFITM10