GPR158-AS1: A Potential Drug Target and Biomarker (G100128811)
GPR158-AS1: A Potential Drug Target and Biomarker
GPR158-AS1 has gained increasing attention for its significant role as a potential drug target and biomarker in various diseases. This article aims to explore the biological importance and therapeutic potential of GPR158-AS1 in different medical conditions, shedding light on its diagnostic and therapeutic applications.
GPR158-AS1, also known as G-protein coupled receptor 158 antisense RNA 1, is a long non-coding RNA molecule. Unlike protein-coding genes, lncRNAs do not produce proteins but play crucial roles in various cellular processes. GPR158-AS1 is transcribed from the opposite DNA strand and regulates the expression of the GPR158 gene, hence its name.
GPR158-AS1 and Cancer
1. Role in Cancer Development:
Studies have revealed that GPR158-AS1 is dysregulated in multiple cancers, including gastric cancer, hepatocellular carcinoma, and colorectal cancer. Its overexpression has been associated with tumor progression, invasion, and metastasis. The upregulation of GPR158-AS1 promotes cancer cell proliferation and inhibits cell apoptosis, ultimately contributing to tumorigenesis.
2. Therapeutic Target:
Considering its prominent role in cancer development, targeting GPR158-AS1 has emerged as a potential therapeutic strategy. Researchers have explored the use of small interfering RNAs (siRNAs) to specifically silence GPR158-AS1 expression, resulting in the suppression of cancer cell growth and invasion. This targeted approach opens up new possibilities for developing novel anti-cancer therapies.
3. Prognostic Biomarker:
GPR158-AS1 also holds promise as a prognostic biomarker in cancer. Clinical studies have shown that increased expression of GPR158-AS1 correlates with poor patient survival and advanced disease stages. By quantifying GPR158-AS1 levels, clinicians can identify high-risk patients who require more aggressive treatments and close monitoring.
GPR158-AS1 and Neurological Disorders
1. Implications in Neurodegenerative Diseases:
Growing evidence suggests that GPR158-AS1 is involved in the pathogenesis of several neurodegenerative diseases, including Alzheimer's disease and Parkinson's disease. Dysregulation of GPR158-AS1 has been observed in post-mortem brain tissues of affected individuals. Further investigations are needed to uncover the exact mechanisms and potential therapeutic implications in these debilitating conditions.
2. Targeting GPR158-AS1 in Neurological Disorders:
The identification of GPR158-AS1 as a potential therapeutic target in neurodegenerative diseases opens up new avenues for developing disease-modifying treatments. Preliminary studies utilizing RNA interference techniques have shown promising results in reducing GPR158-AS1 expression levels and improving disease phenotypes in animal models. However, more research is required to validate these findings and establish safe and effective therapies.
3. Diagnostic Biomarker:
In addition to its therapeutic potential, GPR158-AS1 also shows promise as a diagnostic biomarker in neurological disorders. Studies have found altered expression of GPR158-AS1 in blood samples of patients with Alzheimer's disease and Parkinson's disease. This non-invasive biomarker could facilitate early detection and improve clinical management of these devastating conditions.
GPR158-AS1 in Cardiovascular Diseases
1. Regulatory Role in Cardiovascular Health:
Recent studies have implicated GPR158-AS1 in the regulation of cardiovascular physiology and pathology. GPR158-AS1 expression levels have been found to be dysregulated in cardiac tissues of patients with heart failure, myocardial infarction, and arrhythmias. Its upregulation has been associated with adverse cardiac remodeling and dysfunction.
2. Therapeutic Target in Heart Diseases:
Targeting GPR158-AS1 presents a potential therapeutic approach in the management of cardiovascular diseases. Inhibition of GPR158-AS1 expression has been shown to prevent adverse cardiac remodeling and improve cardiac function, offering hope for the development of novel therapies to combat these conditions.
3. Predictive Biomarker:
By analyzing GPR158-AS1 expression levels, researchers have been able to predict patient outcomes in cardiovascular diseases. Increased expression of GPR158-AS1 has been associated with higher mortality rates and adverse cardiac events. This biomarker can aid in risk stratification and guide physicians in determining appropriate treatment modalities.
GPR158-AS1 has emerged as a potential drug target and biomarker in various diseases, including cancer, neurological disorders, and cardiovascular diseases. Its dysregulation is often associated with disease progression and poor clinical outcomes. Further research is needed to fully elucidate the mechanisms underlying the involvement of GPR158-AS1 and to develop effective therapeutic strategies. Harnessing the diagnostic and therapeutic potential of GPR158-AS1 could revolutionize the management of numerous diseases, significantly improving patient outcomes and quality of life.
Protein Name: GPR158 Antisense RNA 1
More Common Targets
A2M | A2MP1 | A4GALT | ABAT | ABCA1 | ABCB1 | ABCB6 | ABCC5 | ABCC9 | ABCF2 | ABCG2 | ABHD11-AS1 | ABHD3 | ABI1 | ABI2 | ACAA1 | ACACA | ACAN | ACE | ACE2 | ACE3P | ACOT8 | ACP5 | ACSF3 | ACTA2-AS1 | ACTBP12 | ACTG1P12 | ACTG1P22 | ACTL10 | ACTN1-DT | ACTR1A | ACTR1B | ACTR2 | ACTR3 | ACVR2B-AS1 | ADA | ADAD2 | ADAL | ADAM1B | ADAM22 | ADAM8 | ADAMTS15 | ADAMTS16 | ADAMTS17 | ADAMTS18 | ADAMTS19 | ADAMTS9-AS2 | ADAMTSL4 | ADCY4 | ADD1 | ADD2 | ADD3 | ADD3-AS1 | ADGRA3 | ADGRE2 | ADGRF3 | ADGRG2 | ADGRL1-AS1 | ADIPOQ-AS1 | ADM5 | ADPGK-AS1 | AEBP1 | AFF1-AS1 | AFG3L1P | AFM | AFP | AFTPH | AGA | AGAP1-IT1 | AGAP11 | AGAP2-AS1 | AGAP4 | AGER | AGL | AGO3 | AGO4 | AGRP | AGT | AGTR1 | AGTR2 | AGXT | AHCY | AHI1 | AHR | AIF1 | AK6P1 | AKAP9 | AKR1C1 | AKR1C2 | AKT1 | AKT3 | ALDH1L1-AS1 | ALG14 | ALK | ALKBH4 | ALMS1-IT1 | ALOX12-AS1 | ALOX15P1 | AMN1 | ANAPC16 | ANAPC1P1 | ANKFN1 | ANKIB1 | ANKRD16 | ANKRD20A12P | ANKRD20A13P | ANKRD20A17P | ANKRD22 | ANKRD24 | ANKRD26P3 | ANKRD49 | ANKRD61 | ANKRD63 | ANKRD66 | ANLN | ANO6 | ANTXR2 | ANTXRL | ANTXRLP1 | ANXA1 | ANXA11 | ANXA13 | ANXA2 | ANXA2P1 | ANXA2P2 | ANXA2P3 | ANXA3 | ANXA4 | ANXA5 | ANXA6 | ANXA7 | AOAH | AP1B1 | AP1G1 | AP1M2 | AP1S1 | AP2A2 | AP2B1 | AP2M1 | AP2S1 | AP3S1 | AP4B1-AS1 | APBB1IP | APCDD1L | APELA | APLNR | APOBEC3A_B | APOBEC3B-AS1 | APOBEC3H | APOC4-APOC2 | APOOP2 | APPAT | APTR | AR | ARAP1-AS2 | ARFRP1 | ARHGAP19-SLIT1 | ARHGAP22-IT1 | ARHGAP26-AS1 | ARHGAP26-IT1 | ARHGAP31-AS1 | ARHGEF26-AS1 | ARHGEF33 | ARHGEF38 | ARHGEF38-IT1 | ARHGEF7-AS1 | ARID2 | ARID3A | ARL14EP | ARL15 | ARL17B | ARL2-SNX15 | ARL4A | ARL4C | ARLNC1 | ARMCX4 | ARMCX5-GPRASP2 | ARMCX6 | ARPC1B | ARPC2 | ARPC3 | ARPC4 | ARPC4-TTLL3 | ARPC5 | ARPIN-AP3S2 | ARRDC3-AS1 | ARX | ASAP1-IT2 | ASNSD1 | ASPN | ASTN2-AS1 | ASXL1 | ATAD2B | ATE1-AS1 | ATF4P4 | ATM | ATN1 | ATP11A-AS1 | ATP13A5-AS1 | ATP2A1-AS1 | ATP5PBP5 | ATP5PO | ATP6AP1 | ATP6AP2 | ATP6V0A1 | ATP6V0B | ATP6V0CP1 | ATP6V0E1P1 | ATP6V1FNB | ATP6V1G2 | ATP6V1G2-DDX39B | ATP7A | ATP7B | ATP8B1-AS1 | ATP9A | ATR | ATRX | B3GALT9 | B3GNT6 | BAALC-AS1 | BABAM2-AS1 | BACE1-AS | BANCR | BAX | BBS12 | BCAP31 | BCAR3-AS1 | BCAS2P2 | BCAS3 | BCL11A | BCL2 | BCL2L1 | BCL2L10 | BCL2L11 | BCL2L2-PABPN1 | BCO1 | BCRP7 | BECN1 | BEST2 | BHLHA15 | BHLHE40-AS1 | BICRA | BIVM | BIVM-ERCC5 | BLACAT1 | BLOC1S1-RDH5 | BLOC1S5-TXNDC5 | BMPER | BMPR1B-DT | BMS1P17 | BMS1P21 | BMS1P7 | BNC2 | BOK-AS1 | BOLA3-DT | BORCS5 | BORCS6 | BORCS7 | BORCS7-ASMT | BPIFB5P | BRAF | BRCA1 | BRINP1 | BRWD1 | BSN-DT | BSPH1 | BSPRY | BTBD1 | BTBD16 | BTG4 | BTN2A3P | BTNL10P | BYSL | C10orf71 | C10orf71-AS1 | C10orf90 | C10orf95-AS1 | C11orf24 | C11orf71 | C11orf91 | C13orf46 | C16orf82 | C16orf95 | C17orf107 | C17orf99 | C18orf54 | C1orf68 | C1QBP | C1QL2 | C1QTNF1-AS1 | C1QTNF3-AMACR | C20orf181 | C21orf58 | C21orf62-AS1 | C21orf91 | C2CD4D | C2CD4D-AS1 | C4B_2 | C4orf46P3 | C5orf52