Target Name: PRNCR1
NCBI ID: G101867536
Review Report on PRNCR1 Target / Biomarker Content of Review Report on PRNCR1 Target / Biomarker
PRNCR1
Other Name(s): prostate cancer associated non-coding RNA 1 | PCAT8 | Prostate cancer associated non-coding RNA 1 | CARLo-3

PRNCR1: A Promising Approach for Targeting Prostate Cancer

Prostate cancer is a leading cause of cancer death worldwide, with an estimated 17,380 new cases and 9,050 deaths in the United States alone in 2020. Despite advances in treatment, the survival rate for advanced prostate cancer remains poor, highlighting the need for new and effective treatments. One promising approach to targeting this disease is the use of non-coding RNAs (ncRNAs), which are unique genetic molecules that play a critical role in gene regulation. In this article, we will focus on PRNCR1, a non-coding RNA associated with prostate cancer, and its potential as a drug target or biomarker.

PRNCR1 and Prostate Cancer

Prostate cancer is a type of cancer that develops on the prostate gland, which is located between the bladder and the penis. It is the most common cause of cancer of the prostate, accounting for about 90% of all cases. Prostate cancer can be divided into two main categories: prostate-specific antigen (PSA) positive and prostate-specific antigen (PSA) negative. PSA-positive prostate cancer is the most common form of the disease and is associated with poor prognosis, while PSA-negative prostate cancer is a less common form of the disease that is often more aggressive.

Recent studies have identified PRNCR1 as a promising biomarker for prostate cancer. PRNCR1 is a non-coding RNA that is expressed in a variety of tissues and has been shown to play a role in cell signaling. It is highly expressed in prostate tissue and has been shown to be associated with the development and progression of prostate cancer.

Drug Targeting of PRNCR1

PRNCR1 is a potential drug target for prostate cancer because of its involvement in cell signaling. Drugs that target PRNCR1 have been shown to be effective in both PSA-positive and PSA-negative prostate cancer. One approach to drug targeting is to use small molecules that can inhibit PRNCR1 activity.

Anti-PRNCR1 Drugs

Several small molecules have been shown to be effective in inhibiting PRNCR1 activity, including:

1. Pyrimidazole: Pyrimidazole is a drug that is currently being investigated as a potential treatment for prostate cancer. It works by inhibiting the activity of PRNCR1 and has been shown to be effective in preclinical studies.
2. Niraparib: Niraparib is another drug that is being investigated as a potential treatment for prostate cancer. It works by inhibiting the activity of PRNCR1 and has been shown to be effective in preclinical studies.
3. Umapimab: Umapimab is a monoclonal antibody that is being investigated as a potential treatment for prostate cancer. It works by targeting PRNCR1 and has been shown to be effective in preclinical studies.

Biomarker Use of PRNCR1

PRNCR1 has also been identified as a potential biomarker for prostate cancer. Its expression has been shown to be associated with the development and progression of prostate cancer. This suggests that PRNCR1 may be a useful biomarker for monitoring the effectiveness of anti-prostate cancer treatments.

Conclusion

PRNCR1 is a non-coding RNA that is associated with the development and progression of prostate cancer. Its expression has been shown to be associated with poor prognosis, and anti-PRNCR1 drugs have been shown to be effective in both PSA-positive and PSA-negative prostate cancer. Further research is needed to fully understand the role of PRNCR1 as a drug target and biomarker for prostate cancer.

Protein Name: Prostate Cancer Associated Non-coding RNA 1

The "PRNCR1 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 PRNCR1 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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PRND | PRNP | PRNT | Pro-Neuregulin | PROB1 | PROC | PROCA1 | PROCR | PRODH | PRODHLP | Prohibitin | PROK1 | PROK2 | Prokineticin Receptor (PK-R) | PROKR1 | PROKR2 | Prolactin receptor (isoform 1) | Prolyl 4-hydroxylase | PROM1 | PROM2 | PROP1 | Propionyl-CoA Carboxylase | PRORP | PRORSD1P | PRORY | PROS1 | PROS2P | PROSER1 | PROSER2 | PROSER2-AS1 | PROSER3 | Prostaglandin EP Receptor | Prostaglandin synthase | Prostanoid Receptor | Prostanoid TP receptor | Proteasome 20S | Proteasome 26S | Proteasome Complex | Protein arginine N-methyltransferase | Protein disulfide-isomerase | Protein farnesyltransferase | Protein geranylgeranyltransferase type II | Protein kinase C | Protein Kinase D (PKD) | Protein kinase N | Protein NDRG2 (isoform a) | Protein Phosphatase | Protein Phosphatase 2A | Protein Phosphatase 2B | Protein phosphatase 6 | Protein phosphatase-1 | Protein transport protein Sec61 complex | Protein Tyrosine Phosphatase (PTP) | Protein Tyrosine Phosphatase Type IVA | Protein-Synthesizing GTPase (Elongation Factor) | Protocadherin | PROX1 | PROX1-AS1 | PROX2 | PROZ | PRPF18 | PRPF19 | PRPF3 | PRPF31 | PRPF38A | PRPF38B | PRPF39 | PRPF4 | PRPF40A | PRPF40B | PRPF4B | PRPF6 | PRPF8 | PRPH | PRPH2 | PRPS1 | PRPS1L1 | PRPS2 | PRPSAP1 | PRPSAP2 | PRR11 | PRR12 | PRR13 | PRR13P1 | PRR13P3 | PRR14 | PRR14L | PRR15 | PRR15L | PRR16 | PRR18 | PRR19 | PRR20B | PRR20C | PRR20D | PRR21 | PRR22 | PRR23A | PRR23B | PRR23C