Target Name: OSGIN1
NCBI ID: G29948
Review Report on OSGIN1 Target / Biomarker Content of Review Report on OSGIN1 Target / Biomarker
OSGIN1
Other Name(s): BDGI | huOKL38 | OTTHUMP00000174993 | ovary, kidney and liver protein 38 | Oxidative stress induced growth inhibitor 1 | BMSC-derived growth inhibitor | Pregnancy-induced growth inhibitor OKL38 | pregnancy-induced growth inhibitor OKL38 | OSGI1_HUMAN | bone marrow stromal cell-derived growth inhibitor | Bone marrow stromal cell-derived growth inhibitor | OTTHUMP00000174992 | Oxidative stress-induced growth inhibitor 1 | Ovary, kidney and liver protein 38 | OKL38 | oxidative stress induced growth inhibitor 1

OSGIN1: A Non-coding RNA Molecule Involved in Cellular Stress Responses and Potential Drug and Biomarker Targets

OSGIN1 (Oxidative stress-induced gene 1) is a non-coding RNA molecule that has been shown to play a crucial role in the regulation of cellular stress responses. The BDGI (B cell development and integrity) is a key gene for the development and maintenance of B cells, which are a vital part of the immune system. In recent years, researchers have been interested in OSGIN1 as a potential drug target or biomarker, due to its unique expression patterns and its involvement in cellular stress responses.

The OSGIN1 gene was first identified in the rat using RNA interference techniques, and its expression was found to be regulated by several different stress factors, including oxidative stress, UV radiation, and temperature. The gene was then shown to be involved in the regulation of cellular stress responses, by influencing the expression of genes involved in DNA damage repair, cell cycle progression, and apoptosis.

Following these findings, OSGIN1 has been shown to be a potential drug target, with researchers expressing interest in using it as a therapeutic agent to treat a variety of diseases. Studies have shown that OSGIN1 can be effectively targeted to the endoplasmic reticulum (ER), where it can interact with and modulate the activity of various stress-responsive genes. This suggests that OSGIN1 could be an effective drug target by inhibiting the activity of stress-responsive genes, thereby reducing cellular stress and preventing the development of various diseases.

In addition to its potential as a drug target, OSGIN1 has also been shown to be a potential biomarker for a variety of diseases. The expression of OSGIN1 has been shown to be regulated by a variety of factors, including stress, growth factors, and hormones . This suggests that OSGIN1 could be a useful biomarker for evaluating the effectiveness of different therapies in a variety of diseases.

Furthermore, OSGIN1 has also been shown to play a role in the regulation of cellular division and the development of cancer. Studies have shown that OSGIN1 can influence the expression of genes involved in cell division and cell cycle progression, and that its expression is often increased in tissues from cancer-bearing animals. This suggests that OSGIN1 may be involved in the development and progression of cancer, and that it could be a useful target for cancer therapies.

In conclusion, OSGIN1 is a non-coding RNA molecule that has been shown to play a crucial role in the regulation of cellular stress responses. Its unique expression patterns and its involvement in the development and maintenance of B cells make it an interesting potential drug target or biomarker. Further research is needed to fully understand the role of OSGIN1 in cellular stress responses and its potential as a therapeutic agent or biomarker.

Protein Name: Oxidative Stress Induced Growth Inhibitor 1

Functions: Regulates the differentiation and proliferation through the regulation of cell death

The "OSGIN1 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 OSGIN1 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

More Common Targets

OSGIN2 | OSM | OSMR | OSMR-DT | OSR1 | OSR2 | OST4 | OSTC | OSTCP1 | OSTF1 | OSTF1P1 | OSTM1 | OSTM1-AS1 | OSTN | OSTN-AS1 | OTC | OTOA | OTOAP1 | OTOF | OTOG | OTOGL | OTOL1 | OTOP1 | OTOP2 | OTOP3 | OTOR | OTOS | OTP | OTUB1 | OTUB2 | OTUD1 | OTUD3 | OTUD4 | OTUD5 | OTUD6A | OTUD6B | OTUD6B-AS1 | OTUD7A | OTUD7B | OTULIN | OTULINL | OTX1 | OTX2 | OTX2-AS1 | OVAAL | OVCA2 | OVCH1 | OVCH1-AS1 | OVCH2 | OVGP1 | OVOL1 | OVOL1-AS1 | OVOL2 | OVOL3 | OVOS2 | OXA1L | OXA1L-DT | OXCT1 | OXCT1-AS1 | OXCT2 | OXCT2P1 | OXER1 | OXGR1 | OXLD1 | OXNAD1 | OXR1 | OXSM | OXSR1 | OXT | OXTR | Oxysterol-binding protein | Oxysterols receptor LXR | P2RX1 | P2RX2 | P2RX3 | P2RX4 | P2RX5 | P2RX5-TAX1BP3 | P2RX6 | P2RX6P | P2RX7 | P2RY1 | P2RY10 | P2RY10BP | P2RY11 | P2RY12 | P2RY13 | P2RY14 | P2RY2 | P2RY4 | P2RY6 | P2RY8 | P2X Receptor | P2Y purinoceptor | P3H1 | P3H2 | P3H3 | P3H4 | P3R3URF-PIK3R3 | P4HA1