Target Name: PRKCZ-AS1
NCBI ID: G100506504
Review Report on PRKCZ-AS1 Target / Biomarker Content of Review Report on PRKCZ-AS1 Target / Biomarker
PRKCZ-AS1
Other Name(s): cDNA FLJ10346 fis, clone NT2RM2001004 | HCG1770745, isoform CRA_a | cDNA FLJ14128 fis, clone MAMMA1002590 | Uncharacterized protein LOC100506504 | PRKCZ antisense RNA 1

PRKCZ-AS1: A Potential Drug Target and Biomarker

Principal Summary:

PRKCZ-AS1, a novel gene associated with the development of pancreatic cancer, has been identified as a potential drug target and biomarker. The expression of PRKCZ-AS1 has been shown to be significantly associated with poor prognosis in pancreatic cancer patients. Further research is needed to determine the exact mechanisms by which PRKCZ-AS1 contributes to pancreatic cancer development and progression.

Introduction:

Pancreatic cancer is a highly aggressive form of cancer that affects the pancreas, a gland located behind the stomach that produces hormones and digestive enzymes. Despite advances in treatment, the survival rate for pancreatic cancer remains poor, with a five-year survival rate of only around 10%. The development of new drugs and targets for pancreatic cancer is crucial for improving treatment outcomes.

The Identification of PRKCZ-AS1:

PRKCZ-AS1, a gene that encodes a protein known as PRKCZ-AS1, has been identified as a potential drug target and biomarker for pancreatic cancer. The PRKCZ-AS1 gene was discovered through a screening approach using a database of gene expression in cancer. The expression of PRKCZ-AS1 has been shown to be significantly associated with poor prognosis in pancreatic cancer patients, with higher expression levels being associated with a poorer prognosis.

The Function of PRKCZ-AS1:

The function of PRKCZ-AS1 is not yet fully understood, but it is known to play a role in the development and progression of pancreatic cancer. Studies have shown that PRKCZ-AS1 is involved in the regulation of cell adhesion, a process that helps cells stick together and form tissues. In pancreatic cancer, altered cell adhesion has been observed, which may contribute to the development and progression of cancer.

The Potential for Targeting PRKCZ-AS1:

The identification of PRKCZ-AS1 as a potential drug target and biomarker for pancreatic cancer makes it an attractive target for researchers to investigate further. By blocking the activity of PRKCZ-AS1, researchers may be able to reduce the growth and spread of pancreatic cancer cells, leading to improved treatment outcomes. Additionally, PRKCZ-AS1 may also serve as a biomarker for pancreatic cancer, allowing for earlier detection and improved treatment outcomes.

The Future of PRKCZ-AS1 Research:

Further research is needed to fully understand the role of PRKCZ-AS1 in the development and progression of pancreatic cancer. Researchers will need to conduct experiments to determine the exact mechanisms by which PRKCZ-AS1 contributes to cancer development and progression. They will also need to determine the efficacy of targeting PRKCZ-AS1 as a drug target and biomarker for pancreatic cancer.

Conclusion:

In conclusion, PRKCZ-AS1 is a novel gene associated with the development of pancreatic cancer. Its expression has been shown to be significantly associated with poor prognosis in pancreatic cancer patients. Further research is needed to determine the exact mechanisms by which PRKCZ-AS1 contributes to pancreatic cancer development and progression. If PRKCZ-AS1 turns out to be a potential drug target and biomarker for pancreatic cancer, it may lead to improved treatment outcomes for this aggressive form of cancer.

Protein Name: PRKCZ Antisense RNA 1

The "PRKCZ-AS1 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 PRKCZ-AS1 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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PRKD1 | PRKD2 | PRKD3 | PRKDC | PRKG1 | PRKG1-AS1 | PRKG2 | PRKG2-AS1 | PRKN | PRKRA | PRKRIP1 | PRKX | PRKXP1 | PRKY | PRL | PRLH | PRLHR | PRLR | PRM1 | PRM2 | PRM3 | PRMT1 | PRMT2 | PRMT3 | PRMT5 | PRMT5-DT | PRMT6 | PRMT7 | PRMT8 | PRMT9 | PRNCR1 | 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