Friday, April 16, 2010

MicroRNA therapy could be a powerful tool to correct the CSC dysregulation?

Medical Hypothesis: No small matter: microRNAs - key regulators of cancer stem cells by Qing Ji, David Karnak, Ping Hao, Rongquan Wang and Liang Xu, Int J Clin Exp Med 2010(Mar 12); 3(1): 84-7 [FriendFeed entry][Connotea bookmark][Full text via PMC]. PubMed Abstract:
Emerging evidence demonstrates that both tumor suppressor and oncogenic miRNAs play an essential role in stem cell self-renewal and differentiation by negatively regulating the expression of certain key genes in stem cells. It seems logical that they may also be critical players in cancer stem cells. Though small in size, miRNAs play a key role in the epigenetic regulation of cancer stem cells. Specifically, the imbalance of oncogenic vs. tumor suppressor miRNAs may lead to dysregulation of cancer stem cells, thus causing excessive self-renewal and survival of cancer stem cells, and resistance to chemo/radiotherapy. We postulate that restoring the balance of miRNAs will correct this dysregulation via the direct and simultaneous modulation of downstream stem cell pathways involved in cancer stem cell self-renewal and/or differentiation. The resultant restoration of key regulatory pathways could improve therapeutic response. Restoring tumor suppressor miRNAs and/or inhibiting oncogenic miRNAs may provide a novel molecular therapy for human cancers, potentially via modulating cancer stem cells.

Sunday, April 11, 2010

CSC news roundup 2010-04-11

Friday, April 2, 2010

CFI practices called “world’s best’’

The Canada Foundation for Innovation (CFI) is one of the Canadian funding agencies that is a Member of the Cancer Stem Cell Consortium (CSCC). According to a news release from the CFI, dated March 24, 2010, CFI’s Funding Agreement with the Government of Canada required an overall performance evaluation and value-for-money audit (OPEA). Excerpt from the news release: "KPMG conducted an overall performance evaluation and value-for-money audit of the CFI and an international panel of seven experts in global research and research funding reviewed the findings and produced an independent report".

The news release is entitled: Canada Foundation for Innovation practices called “world’s best’’. The full OPEA, performed by KPMG in 2009, as well as the International Review Panel Report, are available via: OPEA Reports and Summary.

Saturday, March 27, 2010

CSC news roundup 2010-03-27

Monday, March 15, 2010

CSC news roundup 2010-03-16

Sunday, March 14, 2010

Conditioned medium induces generation of side population cells

Pluripotency-associated genes in human nasopharyngeal carcinoma CNE-2 cells are reactivated by a unique epigenetic sub-microenvironment by Jun-Xia Cao and 8 co-authors, including Quentin Liu, BMC Cancer 2010(Feb 25); 10: 68 [PubMed citation][Full text via PMC][Full text from journal (via Libre OA)]. Conclusion section of the Abstract:
To our knowledge, this is the first study to demonstrate that non-SP single-clone cells can be induced to generate a SP phenotype when they are cultured with conditioned medium of macrophage-like cells, which is associated with the reactivation of pluripotency-associated genes.

Saturday, March 13, 2010

MicroRNA-34a is a potential therapeutic agent for glioma SC?

See the open-access article: microRNA-34a is tumor suppressive in brain tumors and glioma stem cells by Fadila Guessous and 7 co-authors, including Roger Abounader, Cell Cycle 2010(Mar 18); 9(6) [Epub ahead of print][FriendFeed entry][PubMed citation]. Last 3 sentences of the Abstract:
The new data show that miR-34a expression inhibits various malignancy endpoints in glioma stem cells. Importantly, they also show for the first time that miR-34a expression induces glioma stem cell differentiation. Altogether, the data suggest that miR-34a is a tumor suppressor and a potential potent therapeutic agent that acts by targeting multiple oncogenic pathways in brain tumors and by inducing the differentiation of cancer stem cells.