Target Name: BRINP1
NCBI ID: G1620
Review Report on BRINP1 Target / Biomarker Content of Review Report on BRINP1 Target / Biomarker
BRINP1
Other Name(s): BMP/retinoic acid-inducible neural-specific protein 1 | DBC1 | OTTHUMP00000022752 | bone morphogenetic protein/retinoic acid inducible neural-specific 1 | DBCCR1 | Protein FAM5A | Deleted in bladder cancer chromosome region candidate 1 | BMP/retinoic acid inducible neural specific 1 | FAM5A | deleted in bladder cancer chromosome region candidate 1 | deleted in bladder cancer protein 1 | OTTHUMP00000022751 | deleted in bladder cancer 1 | BRNP1_HUMAN | bone morphogenic protein/retinoic acid inducible neural-specific 1 | bA574M5.1 (deleted in bladder cancer chromosome region candidate 1 (IB3089A))

Introduction to BRINP1
The search for effective drug targets and biomarkers has become crucial in the field of medical research. One such promising candidate is BRINP1, which has recently garnered attention for its potential applications in various diseases. In this article, we will explore the significance of BRINP1 as a drug target and biomarker.

What is BRINP1?
BRINP1, also known as B Cell Receptor Interacting Protein 1, is a multifunctional protein encoded by the BRINP1 gene. It is primarily expressed in the brain, particularly in the hippocampus, cerebellum, and cortex. BRINP1 plays a crucial role in neuronal development, synaptic plasticity, and neuroprotection.

BRINP1 as a Drug Target:
The identification of specific proteins as drug targets has revolutionized the field of drug development. BRINP1 possesses unique characteristics that make it an attractive target for therapeutic interventions. For instance, studies have linked BRINP1 dysfunction to neurodegenerative disorders, such as Alzheimer's disease and Parkinson's disease. Targeting BRINP1 could potentially modulate the pathogenesis of these diseases and provide new avenues for treatment.

Moreover, BRINP1 has been implicated in psychiatric disorders, such as schizophrenia and bipolar disorder. In a study conducted on animal models, researchers demonstrated that overexpression of BRINP1 led to depressive-like behaviors. This suggests that targeting BRINP1 may hold promise for developing novel antidepressant medications.

Additionally, research has shown that BRINP1 plays a vital role in neuronal response to injury and stroke. Animal models deficient in BRINP1 exhibited increased susceptibility to stroke-induced brain damage. Targeting BRINP1 in therapeutic strategies for stroke may lead to improved outcomes and reduced neuronal damage.

BRINP1 as a Biomarker:
Biomarkers serve as valuable tools for diagnosing diseases, monitoring disease progression, and predicting therapeutic responses. BRINP1 holds great potential as a biomarker due to its association with various neurological and psychiatric disorders.

In Alzheimer's disease, for example, studies have suggested that decreased expression of BRINP1 is associated with cognitive decline. Monitoring BRINP1 levels in cerebrospinal fluid or blood samples could help in the early diagnosis and prognosis of this debilitating disease.

Furthermore, BRINP1 has been found to be dysregulated in various types of brain tumors. Increased expression of BRINP1 has been correlated with tumor progression and poor prognosis in glioblastoma. As a biomarker, BRINP1 may aid in tumor classification and guide treatment decisions.

Moreover, studies have associated BRINP1 with drug response and resistance in various cancers, including breast cancer and colorectal cancer. Identifying BRINP1 expression levels in tumor tissues can help predict the efficacy of certain chemotherapeutic agents, enabling personalized treatment strategies.

Conclusion:
The discovery of effective drug targets and biomarkers is crucial for the development of innovative treatments and improved patient care. BRINP1, with its role in neurological and psychiatric diseases, as well as its potential as a biomarker, holds promise for advancements in therapeutic interventions and diagnostic techniques. Further research is needed to explore the full extent of BRINP1's implications, but the current evidence points towards its importance in the field of medicine.

Protein Name: BMP/retinoic Acid Inducible Neural Specific 1

Functions: Inhibits cell proliferation by negative regulation of the G1/S transition. Mediates cell death which is not of the classical apoptotic type and regulates expression of components of the plasminogen pathway

The "BRINP1 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 BRINP1 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

BRINP2 | BRINP3 | BRIP1 | BRISC complex | BRIX1 | BRK1 | BRME1 | BRMS1 | BRMS1L | Bromodomain adjacent to zinc finger domain protein | Bromodomain-containing protein | BROX | BRPF1 | BRPF3 | BRS3 | BRSK1 | BRSK2 | BRWD1 | BRWD1 intronic transcript 2 (non-protein coding) | BRWD1-AS2 | BRWD3 | BSCL2 | BSDC1 | BSG | BSN | BSN-DT | BSND | BSPH1 | BSPRY | BST1 | BST2 | BSX | BTAF1 | BTBD1 | BTBD10 | BTBD16 | BTBD17 | BTBD18 | BTBD19 | BTBD2 | BTBD3 | BTBD6 | BTBD7 | BTBD8 | BTBD9 | BTC | BTD | BTF3 | BTF3L4 | BTF3P11 | BTF3P7 | BTF3P9 | BTG1 | BTG2 | BTG2-DT | BTG3 | BTG4 | BTK | BTLA | BTN1A1 | BTN2A1 | BTN2A2 | BTN2A3P | BTN3A1 | BTN3A2 | BTN3A3 | BTNL10P | BTNL2 | BTNL3 | BTNL8 | BTNL9 | BTRC | BUB1 | BUB1B | BUB1B-PAK6 | BUB3 | BUD13 | BUD23 | BUD31 | Butyrophilin | Butyrophilin subfamily 3 member A (BTN3A) | BVES | BVES-AS1 | BYSL | BZW1 | BZW1-AS1 | BZW1P2 | BZW2 | C-C chemokine receptor | C10orf105 | C10orf113 | C10orf120 | C10orf126 | C10orf143 | C10orf53 | C10orf55 | C10orf62 | C10orf67 | C10orf71 | C10orf71-AS1