| CFC1B | |||||||||||||||||||||||||||||||||||||||||||||||||||
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| Identifiers | |||||||||||||||||||||||||||||||||||||||||||||||||||
| Aliases | CFC1B, entrez:653275, cripto, FRL-1, cryptic family 1B | ||||||||||||||||||||||||||||||||||||||||||||||||||
| External IDs | MGI:109448;HomoloGene:50007;GeneCards:CFC1B;OMA:CFC1B - orthologs | ||||||||||||||||||||||||||||||||||||||||||||||||||
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| Wikidata | |||||||||||||||||||||||||||||||||||||||||||||||||||
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Cripto is an EGF-CFC or epidermal growth factor-CFC, which is encoded by the Cryptic family 1 gene.[5]Cryptic family protein 1B is a protein that in humans is encoded by theCFC1B gene.[6][7] Cryptic family protein 1B acts as a receptor for theTGF beta signaling pathway. It has been associated with the translation of an extracellular protein for this pathway.[5] The extracellular protein which Cripto encodes plays a crucial role in the development of left and right division of symmetry.[8]
Crypto is a glycosylphosphatidylinositol-anchored co-receptor that bindsnodal and the activin type I ActRIB (ALK)-4 receptor (ALK4).[5][9][10]
Cripto is composed of two adjacentcysteine-rich motifs: the EGF-like and theCFC of anN-terminal signal peptide and of aC-terminalhydrophobic region attached by a GPI anchor,[11] which makes it a potentially essential element in the signaling pathway directing vertebrate embryo development.[12] NMR data confirm that the CFC domain has a C1-C4, C2-C6, C3-C5 disulfide pattern and show that structures are rather flexible and globally extended, with three non-canonical anti-parallel strands.[11]
In the Nodal signaling pathway of embryonic development, Cripto has been shown to have dual function as a co-receptor as well as ligand. Particularly in cell cultures, it has been shown to act as a signaling molecule with the capabilities of a growth factor, and in co-culture assays, it has displayed the property of a co-ligand to Nodal. Glycosylation is responsible for mediating this interface with Nodal. EGF-CFC proteins’ composition as a receptor complex is further solidified by the GPI linkage, making the cell membrane connection able to regulate growth factor signaling of Nodal.[5]
High concentrations of Cripto are found in both the trophoblast and inner cell mass, along the primitive streak as the second epithelial-mesenchymal transformation event occurs to form themesoderm, and in the myocardium of the developing heart. Though no specific defect has been formally associated with mutations in Cripto, in vitro studies that disrupt gene function at various times during development have provided glimpses of possible malformations. For example, inactivation of Cripto during gastrulation disrupted the migration of newly formed mesenchymal mesoderm cells, resulting in the accumulation of cells around the primitive streak and eventualembryonic death.[13] Other results of Cripto disruption include the lack of posterior structures.[14] and a block on the differentiation of cardiac myocyte,.[15] both of which lead to embryonic death.
Cripto's functions have been hypothesized from these null mutation studies. It is now known that Cripto is similar to other morphogens originating from the primitive streak in that it is asymmetrically expressed, specifically in a proximal-distal gradient,[14] explaining the failure of posterior structures to form in the absence of Cripto.
The high expression of Cripto-1 was detected in many types of cancer such as pancreatic, breast and colon cancer. The high expression levels were linked to poor survival rate in cancer patients. Its role was suggested to be through promotion ofepithelial-to-mesenchymal transition (EMT). TheWnt signaling pathway/β-catenin and TGF-B/Smad pathway was shown to control epithelial-to-mesenchymal transition in cancer.[16][17] Recently, Cripto-1 was proposed as cancer stem cell marker.
CFC1B hasoncogene potential[11] due to the tumor cell proliferation through initiation by autocrine or paracrine signaling.[5] Furthermore, the cryptic protein is highly over-expressed in many tumors[11] such as colorectal, gastric, breast, and pancreatic cancers in homosapiens.[5] Cripto is one of the key regulators ofembryonic stem cells differentiation intocardiomyocyte vs.neuronal fate.[18] Expression levels of cripto are associated with resistance toEGFR inhibitors.[19]
Teratocarcinoma-derived growth factor 1
