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How do a cancer cell pass blood-brain barrier?


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Hi everyone, I have had a questionmark about a point in my mind for a long time : While its hard for even a procaryotic bacterium to pass blood-brain barrier (to me, because of tight junctions between endothelial cells), how is it possible to pass it for a eucaryotic cancer cell and metastasize to the brain?

If you enlighten me about it, I will be :)

Thank you.

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Warning: I am not a cancer biologist.

 

Based on an educated guess and some quick reading, the mechanism is: the cancer cells are able to attach to the endothelium, unzip the intracellular zipper and squeeze through. This has to do with the cancer cells having what amounts to half a zipper all over their surface. They unzip the zipper between the endothelial cells and zip themselves into the space. Then they rezip the zipper as they pass through. Beautiful! Leukocytes are capable of doing this by the same mechanism, crossing the BBB with ease.

 

The reason microbes cannot do this is that they don't have the zipper molecules on their surface (in fact, they have stuff on their surface that will make the endothelial cells very angry).

 

Here are two articles with sections that would be good (I love Nature Reviews, there should be a Nature Reviews Med School Admissions journal):

http://www.ncbi.nlm.nih.gov/pubmed/21472002

http://www.ncbi.nlm.nih.gov/pubmed/21365651

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Thank you EoE.. in a CD of a book about cell molecular biology I have watched a photomicrographed film of a piece of scarred tissue, and yes:) it was really beautiful, even exciting.. the leukocyte was passing through the endothelial cells just like tooth paste coming out of tube.

So there is no protective role of BBB on metastasis.

 

Thank you for the links as well.. lets read them:)

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Cancer cells(the ones which can) are damaging the tight junctions and once they open a path, it becomes easier for the other cancer cells coming after..

what a plague this cancer is! its not only proliferating in itself, but also producing enzymes, getting free of extracellular matrix, promoting angiogenensis.. as if well organized.. sometimes it becomes hard to believe that those all occur coincidentially..

 

http://www.plosone.org/article/info%3Adoi%2F10.1371%2Fjournal.pone.0020758

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