Target Name: C7
NCBI ID: G730
Review Report on C7 Target / Biomarker Content of Review Report on C7 Target / Biomarker
C7
Other Name(s): complement component 7 | Complement C7 | Complement component C7 | CO7_HUMAN | complement C7

C7: A Promising Drug Target and Biomarker for the Treatment of Chronic Pain

Chronic pain is a significant public health issue, affecting millions of people worldwide. The World Health Organization (WHO) estimates that 500 million people experience chronic pain, representing 12% of the global population. Chronic pain can be caused by various conditions, including musculoskeletal, rheumatoid, and neuropathic pain. The management of chronic pain is a complex and multifaceted approach that requires a combination of medical, psychological, and social interventions.

Complement component 7 (C7) is a protein that plays a crucial role in the immune response and inflammation. It is a member of the complement system, which is a group of proteins that work together to help the immune system fight off infections and diseases. C7 is involved in the formation of the C7a subunit, which is a key component of the complement system.

Recent studies have suggested that C7 may have a potential as a drug target for the treatment of chronic pain. This is because C7 has been shown to play a role in the regulation of pain signaling and the modulation of pain perception.

The Potential Role of C7 in Chronic Pain

Chronic pain can be caused by various factors, including inflammation, inflammation-mediated pain, and neuroinflammation. C7 is involved in the regulation of these processes, which may explain its potential as a drug target for chronic pain.

First, C7 is involved in the regulation of pain signaling. C7a is a protein that plays a key role in the formation of the complement system, and it has been shown to regulate the activity of pain-sensitive neurons. C7a has been shown to enhance the sensitivity of pain-sensitive neurons to pain stimuli, which may contribute to the development of chronic pain.

Second, C7 is involved in the regulation of inflammation. C7 is a potent regulator of inflammation, and it has been shown to play a role in the regulation of immune cell function and the production of pro-inflammatory cytokines. Chronic pain is often associated with inflammation in the central nervous system, and targeting C7 with drugs that can modulate its activity may be an effective way to treat chronic pain.

Third, C7 may be involved in the modulation of pain perception. C7 has been shown to play a role in the regulation of pain perception, and it has been shown to modulate the activity of pain-sensitive neurons. This may explain why C7 has been shown to have a potential as a pain-modulating drug in animal models of chronic pain.

Drugs that can modulate the activity of C7 may have a potential as a treatment for chronic pain. For example, studies have shown that inhibitors of C7a can effectively reduce pain sensitivity in animal models of chronic pain. Similarly, drugs that can modulate the activity of C7 may be effective in treating chronic pain in humans.

Conclusion

C7 is a protein that has been shown to play a role in the regulation of pain signaling, inflammation, and pain perception. Its potential as a drug target for chronic pain makes it an attractive target for future research. Further studies are needed to fully understand the role of C7 in chronic pain and to develop effective treatments.

Protein Name: Complement C7

Functions: Constituent of the membrane attack complex (MAC) that plays a key role in the innate and adaptive immune response by forming pores in the plasma membrane of target cells. C7 serves as a membrane anchor

The "C7 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 C7 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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C7orf13 | C7orf25 | C7orf31 | C7orf33 | C7orf50 | C7orf57 | C8A | C8B | C8G | C8orf33 | C8orf34 | C8orf34-AS1 | C8orf44 | C8orf48 | C8orf58 | C8orf74 | C8orf76 | C8orf82 | C8orf88 | C8orf89 | C9 | C9orf131 | C9orf152 | C9orf153 | C9orf163 | C9orf24 | C9orf40 | C9orf43 | C9orf47 | C9orf50 | C9orf57 | C9orf64 | C9orf72 | C9orf78 | C9orf78P2 | C9orf85 | CA1 | CA10 | CA11 | CA12 | CA13 | CA14 | CA15P1 | CA2 | CA3 | CA3-AS1 | CA4 | CA5A | CA5B | CA5BP1 | CA6 | CA7 | CA8 | CA9 | CAAP1 | CAB39 | CAB39L | CABCOCO1 | CABIN1 | CABLES1 | CABLES2 | CABP1 | CABP2 | CABP4 | CABP5 | CABP7 | CABS1 | CABYR | CACFD1 | CACHD1 | CACNA1A | CACNA1B | CACNA1C | CACNA1C-AS4 | CACNA1C-IT2 | CACNA1C-IT3 | CACNA1D | CACNA1E | CACNA1F | CACNA1G | CACNA1G-AS1 | CACNA1H | CACNA1I | CACNA1S | CACNA2D1 | CACNA2D1-AS1 | CACNA2D2 | CACNA2D3 | CACNA2D4 | CACNB1 | CACNB2 | CACNB3 | CACNB4 | CACNG1 | CACNG2 | CACNG2-DT | CACNG3 | CACNG4 | CACNG5 | CACNG6