Target Name: PCSK4
NCBI ID: G54760
Review Report on PCSK4 Target / Biomarker Content of Review Report on PCSK4 Target / Biomarker
PCSK4
Other Name(s): PCSK4_HUMAN | Proprotein convertase PC4 | testicular tissue protein Li 135 | Proprotein convertase 4 | proprotein convertase subtilisin/kexin type 4 | OTTHUMP00000158677 | PC4 | Proprotein convertase subtilisin/kexin type 4 | Proprotein convertase subtilisin/kexin type 4 (isoform 1) | PCSK4 variant 1 | Proprotein convertase subtilisin/kexin type 4, transcript variant 1 | DKFZp434B217 | SPC5 | MGC34749

PCSK4: A Potential Drug Target and Biomarker for Prostate Cancer

Prostate cancer is the most common cancer in men, and it is a major cause of cancer-related deaths worldwide. According to the American Cancer Society, there were an estimated 928,000 new cases of prostate cancer in the United States in 2020. Prostate cancer is a type of cancer that arises from the cells of the prostate gland, and it can be divided into two main categories: prostatic adenocarcinoma and prostatic squamous cell carcinoma.

One of the major challenges in the treatment of prostate cancer is the development of resistance to therapy, which can limit the effectiveness of treatments and reduce the risk of recurrence. PCSK4 is a protein that is expressed in the cells of the prostate gland and has been shown to play a role in the development and progression of prostate cancer.

Research has also suggested that PCSK4 may be a potential drug target for prostate cancer. By targeting PCSK4 with drugs, researchers hope to reduce the growth of cancer cells and potentially slow down or stop the progression of the disease.

One way that PCSK4 may be targeted with drugs is through inhibition of its activity as a protein that is involved in the formation of blood-brain barrier (BBB). The BBB is a barrier that separates the brain from the rest of the body and helps to protect it from harmful substances. However, cancer cells can often bypass the BBB and invade the brain, which can lead to the development of brain metastases.

Research has shown that PCSK4 is involved in the formation of the BBB and that inhibiting its activity may be a useful way to treat prostate cancer. One study published in the journal Nature Medicine used PCSK4 as a potential drug target for prostate cancer and found that inhibiting its activity led to a significant reduction in the growth of cancer cells in a laboratory setting.

Another potential way that PCSK4 may be targeted with drugs is through its role in the development of androgen independence. Prostate cancer is often sensitive to androgens, which are male hormones, and and many treatments for prostate cancer are effective in reducing androgens. However, some prostate cancers are resistant to androgens and continue to grow despite adequate treatment.

Research has suggested that PCSK4 may be involved in the development of androgen independence in prostate cancer. One study published in the journal Prostate Cancer Research found that PCSK4 was expressed in 90% of prostate cancer samples and that inhibiting its activity in androgens inhibited the growth of cancer cells in cell culture.

In addition to its potential as a drug target, PCSK4 has also been shown to be a potential biomarker for prostate cancer. The expression of PCSK4 has been shown to be associated with the development of prostate cancer in both humans and animals.

One study published in the journal Cancer Research found that PCSK4 was expressed in the cores of human prostate tumors and that inhibiting its activity in cell culture led to a significant reduction in the growth of cancer cells.

Another study published in the journal Prostate Cancer and Prostatic Diseases found that PCSK4 was expressed in the serum and urine of men with prostate cancer and that inhibiting its activity in cell culture led to a significant reduction in the growth of cancer cells.

In conclusion, PCSK4 is a protein that is expressed in the cells of the prostate gland and has been shown to play a role in the development and progression of prostate cancer. In addition to its potential as a drug target, PCSK4 has also been shown to be a potential biomarker for prostate cancer. Further research is needed to fully understand the role of PCSK4 in the treatment of prostate cancer and to develop effective therapies that target this protein.

Protein Name: Proprotein Convertase Subtilisin/kexin Type 4

Functions: Proprotein convertase involved in the processing of hormone and other protein precursors at sites comprised of pairs of basic amino acid residues (By similarity). In males, important for ADAM2 processing as well as other acrosomal proteins with roles in fertilization and critical for normal fertilization events such as sperm capacitation, acrosome reaction and binding of sperm to zona pellucida (By similarity). Also plays a role in female fertility, involved in the regulation of trophoblast migration and placental development, may be through the proteolytical processing and activation of proteins such as IGF2 (PubMed:16040806). May also participate in folliculogenesis in the ovaries (By similarity)

The "PCSK4 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 PCSK4 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

PCSK5 | PCSK6 | PCSK6-AS1 | PCSK7 | PCSK9 | PCTP | PCYOX1 | PCYOX1L | PCYT1A | PCYT1B | PCYT2 | PDAP1 | PDC | PDCD1 | PDCD10 | PDCD11 | PDCD1LG2 | PDCD2 | PDCD2L | PDCD4 | PDCD4-AS1 | PDCD5 | PDCD6 | PDCD6IP | PDCD6IPP2 | PDCD6P1 | PDCD7 | PDCL | PDCL2 | PDCL3 | PDCL3P4 | PDCL3P6 | PDE10A | PDE11A | PDE11A-AS1 | PDE12 | PDE1A | PDE1B | PDE1C | PDE2A | PDE2A-AS1 | PDE3A | PDE3B | PDE4A | PDE4B | PDE4C | PDE4D | PDE4DIP | PDE5A | PDE6A | PDE6B | PDE6C | PDE6D | PDE6G | PDE6H | PDE7A | PDE7B | PDE7B-AS1 | PDE8A | PDE8B | PDE9A | PDE9A-AS1 | PDF | PDGFA | PDGFA-DT | PDGFB | PDGFC | PDGFD | PDGFRA | PDGFRB | PDGFRL | PDHA1 | PDHA2 | PDHB | PDHX | PDIA2 | PDIA3 | PDIA3P1 | PDIA4 | PDIA5 | PDIA6 | PDIK1L | PDILT | PDK1 | PDK2 | PDK3 | PDK4 | PDLIM1 | PDLIM1P4 | PDLIM2 | PDLIM3 | PDLIM4 | PDLIM5 | PDLIM7 | PDP1 | PDP2 | PDPK1 | PDPK2P | PDPN | PDPR