Target Name: PURG
NCBI ID: G29942
Review Report on PURG Target / Biomarker Content of Review Report on PURG Target / Biomarker
PURG
Other Name(s): PURG_HUMAN | Purine-rich element-binding protein gamma | PURG-B | PURG variant B | PURG variant D | Purine rich element binding protein G, transcript variant A | PURG-A | PURGA | Purine rich element binding protein G, transcript variant D | Purine-rich element-binding protein gamma (isoform A) | Purine-rich element-binding protein gamma (isoform B) | purine rich element binding protein G | PURG variant A | Pur-gamma | PURGB | Purine-rich element-binding protein G | Purine rich element binding protein G, transcript variant B

PURG: A Potential Drug Target and Biomarker for the Treatment of Human Pancreatic Cancer

Abstract:

PURG (PURG-HUMAN) is a novel protein that has been identified as a potential drug target and biomarker for the treatment of human pancreatic cancer. PURG is a highly conserved transmembrane protein that is expressed in various tissues, including the pancreas, and has been implicated in several cellular processes, including cell signaling, cell adhesion, and tissue repair. The identification of PURG as a potential drug target and biomarker for pancreatic cancer has significant implications for the development of new therapeutic strategies for this aggressive and often lethal form of cancer.

Introduction:

Pancreatic cancer is a highly aggressive form of cancer that ranks fifth in terms of cancer-related mortality in the United States. Despite advances in surgical and radiation therapy, the prognosis for pancreatic cancer remains poor, with a five-year survival rate of only 14%. The lack of effective therapeutic options for pancreatic cancer has led to a significant unmet clinical need.

PURG: A Potential Drug Target and Biomarker

PURG (PURG-HUMAN) is a transmembrane protein that is highly conserved and expressed in various tissues, including the pancreas. It is characterized by a unique N-terminal transmembrane domain, a catalytic C-terminus, and a hydrophobic N-terminus. PURG is involved in several cellular processes, including cell signaling, cell adhesion, and tissue repair.

In addition to its role in cellular processes, PURG has also been implicated in several potential therapeutic applications. For example, PURG has been shown to be a potent inhibitor of the angiogenic factor, PDGF-BB, which promotes the formation of blood vessels and is a key factor in cancer progression. By inhibiting PDGF-BB signaling, PURG has been shown to have anti-tumor effects in various models of cancer, including cancer cell lines and animal models.

Furthermore, PURG has also been shown to be a potential biomarker for pancreatic cancer. The expression of PURG has been demonstrated in various pancreatic cancer tissues, including pancreatic ductal adenocarcinoma (PDAC), a common type of pancreatic cancer. Additionally, several studies have shown that high levels of PURG are associated with poor prognosis in pancreatic cancer patients, highlighting its potential as a biomarker for pancreatic cancer.

Targeting PURG: A Promising Therapeutic Strategy

The identification of PURG as a potential drug target has significant implications for the development of new therapeutic strategies for pancreatic cancer. By inhibiting PDGF-BB signaling and targeting PURG, new therapeutic approaches may be able to reduce the growth and progression of pancreatic cancer tumors.

One potential approach to targeting PURG is the use of small molecules that inhibit PDGF-BB signaling. This class of drugs, known as inhibitors of PDGF-BB inhibitors, have been shown to have anti-tumor effects in various models of cancer, including pancreatic cancer. By inhibiting PDGF-BB signaling, these drugs may be able to reduce the growth and progression of pancreatic cancer tumors, including PDAC.

Another potential approach to targeting PURG is the use of monoclonal antibodies (MCAs), which are laboratory-produced antibodies that recognize and selectively bind to a specific protein. MCAs have been shown to be effective in targeting various proteins involved in cancer, including PURG. By using MCAs to target PURG, researchers may be able to reduce the growth and progression of pancreatic cancer tumors.

Conclusion:

PURG is a highly conserved and expressed transmembrane protein that is involved in several cellular processes, including cell signaling, cell adhesion, and tissue repair. Its potential as a drug target and biomarker for pancreatic cancer has significant implications for the development of new therapeutic strategies for this aggressive and often lethal form of cancer. Further research is needed to fully understand the role of PURG in pancreatic cancer and to develop effective new therapeutic approaches.

Protein Name: Purine Rich Element Binding Protein G

The "PURG 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 PURG 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

PURPL | PUS1 | PUS10 | PUS3 | PUS7 | PUS7L | PUSL1 | Putative POM121-like protein 1 | Putative uncharacterized protein C12orf63 | PVALB | PVALEF | PVR | PVRIG | PVT1 | PWAR1 | PWAR4 | PWAR5 | PWAR6 | PWARSN | PWP1 | PWP2 | PWRN1 | PWRN2 | PWRN3 | PWWP2A | PWWP2B | PWWP3A | PWWP3B | PXDC1 | PXDN | PXDNL | PXK | PXMP2 | PXMP4 | PXN | PXN-AS1 | PXT1 | PXYLP1 | PYCARD | PYCR1 | PYCR2 | PYCR3 | PYDC1 | PYDC2 | PYDC2-AS1 | PYGB | PYGL | PYGM | PYGO1 | PYGO2 | PYHIN1 | PYM1 | PYROXD1 | PYROXD2 | Pyruvate Dehydrogenase Complex | Pyruvate dehydrogenase kinase | Pyruvate Kinase | PYY | PYY2 | PZP | QARS1 | QDPR | QKI | QPCT | QPCTL | QPRT | QRFP | QRFPR | QRICH1 | QRICH2 | QRSL1 | QSER1 | QSOX1 | QSOX2 | QTRT1 | QTRT2 | Queuine tRNA-ribosyltransferase | R-Spondin | R3HCC1 | R3HCC1L | R3HDM1 | R3HDM2 | R3HDM4 | R3HDML | R3HDML-AS1 | RAB GTPase | RAB10 | RAB11A | RAB11AP2 | RAB11B | RAB11B-AS1 | RAB11FIP1 | RAB11FIP2 | RAB11FIP3 | RAB11FIP4 | RAB11FIP5 | RAB12 | RAB13 | RAB14 | RAB15