The Wnt / Beta-Catenin Pathway and Familial Adenomatous Polyposis Part 4

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Elliot Nicholson

Elliot Nicholson

Күн бұрын

Familial Adenomatous Polyposis (FAP) is an inherited genetic condition which predisposes individuals to the formation of colonic polyps. Individuals with the condition typically end up with a colon that is full of polyps.
Familial Adenomatous Polyposis is caused by an inherited mutation in one of the copies of the gene for the APC protein (Adenomatous Polyposis Coli protein, named such because of its involvement in this condition). This protein is involved in an important intracellular signalling mechanism called the Wnt/Beta-Catenin pathway which is involved in controlling cellular division. Mutations in the APC genes result in loss of function of the protein. If both genes are lost inside a cell, then that cell will have no functional APC protein. This results in complete disfunction of the Wnt/Beta-Catenin pathway and the cell ends up dividing excessively producing a whole population of cells with the same mutation. When this occurs in colonic epithelial cells, it physically manifests as a polyp.
An individual with two normal inherited APC genes needs a colonic epithelial cell to have suffered loss of function mutations of both APC genes in order for a polyp to arise. Individuals with Familial Adenomatous Polyposis have one inherited mutation already. So for their colonic epithelial cells it is only necessary for them to acquire one mutation in order for a polyp to arise. This one hit is far more likely than the two hits it would take for someone without the inherited mutation. Hence it occurs far more frequently and individuals with FAP end up with far more polyps.
In this video we discuss the Wnt / Beta-catenin pathway in detail and where the APC protein fits into this pathway. From this we can understand how loss of the APC protein would lead to excessive cell division. We then discuss FAP in which the inherited loss of one of the APC genes means that if a cell were to develop a mutation in the second of the two genes it would lose control of this pathway and excessive division would follow. Indeed this is what happens for these individuals and the most predisposed location for the second genetic hit to occur is the colonic epithelial cells and this is where they end up with multiple tumours.

Пікірлер: 7
@shazxx1992
@shazxx1992 9 жыл бұрын
may I just say I was having a very hard time studying this topic for my exam, but with the aid of this video I think I finally understand it! thank you very much :)
@m.y.515
@m.y.515 9 жыл бұрын
I am starting research in a lab focusing on small molecule inhibitors that target the Wnt/b-catenin pathway. I watched all four of your videos and found them very beneficial. Thank you for taking the time to put these up!
@kvvful
@kvvful 9 жыл бұрын
thank you so much for teaching us how the Wnt signalling works really helps my research. Please keep doing more videos like this.
@skmaj08
@skmaj08 8 жыл бұрын
Great videos! Made my research project so much easier.
@bennie2
@bennie2 9 жыл бұрын
Hi, I have seen in papers that the FAP is inherited in an autosomal dominant pattern. Does this mean that the Two-hit hypothesis isn't the case for APC? Thank you for the video!
@vyjayanthi6775
@vyjayanthi6775 6 жыл бұрын
Same doubt
@mrj1247
@mrj1247 5 жыл бұрын
You are a god!
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