Calreticulin, a therapeutic target?. (1st September 2016)
- Record Type:
- Journal Article
- Title:
- Calreticulin, a therapeutic target?. (1st September 2016)
- Main Title:
- Calreticulin, a therapeutic target?
- Authors:
- Eggleton, Paul
Bremer, Edwin
Dudek, Elzbieta
Michalak, Marek - Abstract:
- ABSTRACT: Introduction : Calreticulin is an endoplasmic reticulum (ER) resident protein critical for maintaining Ca 2+ homeostasis and glycoprotein folding in the ER. The protein has also been identified on the cell surface of apoptotic and necrotic cells and implicated to play a role in immunogenic cell death and other extracellular functions. The molecular events that promote cell surface association of calreticulin are not clear. Under cell stress conditions (environmental, drug induced, hypoxia), calreticulin may be upregulated as it attempts to regulate cell survival, death or repair. The initial signaling mechanisms involved in these processes may be regulated by the unfolded protein response (UPR) and genome damage response (GDR) pathways. Area covered : Here, the phenomenon of cell surface calreticulin and its extracellular functions are discussed, with a major emphasis on the process of immunogenic cell death. The evidence of how cell surface calreticulin may act as a damage associated molecular pattern molecule is evaluated, in addition to how these properties of the protein can be exploited for therapeutic vaccine development, cancer treatment and mediating other inflammatory processes. In addition, clarification of calreticulin functions from its intracellular, cell surface, and extracellular locations are provided. Expert opinion : While the protein folding and immune-stimulatory properties of calreticulin can be exploited to develop therapies, the molecularABSTRACT: Introduction : Calreticulin is an endoplasmic reticulum (ER) resident protein critical for maintaining Ca 2+ homeostasis and glycoprotein folding in the ER. The protein has also been identified on the cell surface of apoptotic and necrotic cells and implicated to play a role in immunogenic cell death and other extracellular functions. The molecular events that promote cell surface association of calreticulin are not clear. Under cell stress conditions (environmental, drug induced, hypoxia), calreticulin may be upregulated as it attempts to regulate cell survival, death or repair. The initial signaling mechanisms involved in these processes may be regulated by the unfolded protein response (UPR) and genome damage response (GDR) pathways. Area covered : Here, the phenomenon of cell surface calreticulin and its extracellular functions are discussed, with a major emphasis on the process of immunogenic cell death. The evidence of how cell surface calreticulin may act as a damage associated molecular pattern molecule is evaluated, in addition to how these properties of the protein can be exploited for therapeutic vaccine development, cancer treatment and mediating other inflammatory processes. In addition, clarification of calreticulin functions from its intracellular, cell surface, and extracellular locations are provided. Expert opinion : While the protein folding and immune-stimulatory properties of calreticulin can be exploited to develop therapies, the molecular pathways involved remain to be elucidated. Nevertheless, exploiting the multifaceted properties of calreticulin may in the future provide a means to treat a number of diseases. … (more)
- Is Part Of:
- Expert opinion on therapeutic targets. Volume 20:Number 9(2016:Sep.)
- Journal:
- Expert opinion on therapeutic targets
- Issue:
- Volume 20:Number 9(2016:Sep.)
- Issue Display:
- Volume 20, Issue 9 (2016)
- Year:
- 2016
- Volume:
- 20
- Issue:
- 9
- Issue Sort Value:
- 2016-0020-0009-0000
- Page Start:
- 1137
- Page End:
- 1147
- Publication Date:
- 2016-09-01
- Subjects:
- Calreticulin -- endoplasmic reticulum -- immunogenic cell death -- cancer
Drugs -- Research -- Periodicals
615.072 - Journal URLs:
- http://informahealthcare.com/journal/ett ↗
http://informahealthcare.com ↗
http://juno.ashley-pub.com/vl=2061206/cl=65/nw=1/rpsv/journal/journal8_home.htm ↗ - DOI:
- 10.1517/14728222.2016.1164695 ↗
- Languages:
- English
- ISSNs:
- 1744-7631
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3842.002965
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 4.xml