Volume 1, Issue 3 (8-2011)                   NCMBJ 2011, 1(3): 75-88 | Back to browse issues page

XML Persian Abstract Print


Ferdowsi University of Mashhad , hamid.ch65@gmail.com
Abstract:   (26688 Views)
Normal 0 false false false EN-US X-NONE AR-SA

Aim and Background. Glioblastoma tumour cells release microvesicles (exosomes) containing mRNA, miRNA and angiogenic proteins. These microvesicles are taken up by normal host cells, such as brain microvascular endothelial cells.

 
 

Materials and methods. By incorporating an mRNA for a reporter protein into these microvesicles, we demonstrate that messages delivered by microvesicles are translated by recipient cells. These microvesicles are also enriched in angiogenic proteins and stimulate tubule formation by endothelial cells.

Results. Tumour-derived microvesicles therefore serve as a means of delivering genetic information and proteins to recipient cells in the tumour environment. Glioblastoma microvesicles also stimulated proliferation of a human glioma cell line, indicating a self-promoting aspect. Messenger RNA mutant/variants and miRNAs characteristic of gliomas could be detected in serum microvesicles of glioblastoma patients. The tumour-specific EGFRvIII was detected in serum microvesicles from 7 out of 25 glioblastoma patients.

 

Conclusion. The tumour-specific EGFRvIII was detected in serum microvesicles from 7 out of 25 glioblastoma patients. Thus, tumour-derived microvesicles may provide diagnostic information and aid in therapeutic decisions for cancer patients through a blood test.

 
Full-Text [PDF 1735 kb]   (174 Downloads)    
Type of Study: Short Communication | Subject: Cellular and molecular
Received: 2011/08/11 | Published: 2011/08/15

Rights and permissions
Creative Commons License This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License.