meeting-report
The 5th International Society for Stem Cell Research (ISSCR) Annual Meeting, June 2007
Article first published online: 25 OCT 2007
DOI: 10.1634/stemcells.2007-0647
Copyright © 2008 AlphaMed Press
Additional Information
How to Cite
Rajasekhar, V. K., Dalerba, P., Passegué, E., Lagasse, E. and Najbauer, J. (2008), The 5th International Society for Stem Cell Research (ISSCR) Annual Meeting, June 2007. STEM CELLS, 26: 292–298. doi: 10.1634/stemcells.2007-0647
Publication History
- Issue published online: 2 JAN 2009
- Article first published online: 25 OCT 2007
- Manuscript Accepted: 15 OCT 2007
- Manuscript Received: 14 AUG 2007
- Abstract
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- References
- Cited By
Keywords:
- Aberrant differentiation;
- Adult stem cells;
- Cancer stem cells;
- Epigenetic alterations;
- Glioblastoma Hematopoietic stem cells;
- Metastasis;
- Polycomb group proteins;
- Self-renewal;
- Stem cell maintenance Stem cell niche;
- Tumor microenvironment;
- Tumor stroma
Abstract
This report presents highlights of discussions that focused on the biology of cancer stem cells as conducted at the fifth Annual Meeting of the International Society for Stem Cell Research, held in Cairns, Australia, June 17–20, 2007. The function of adult stem cells is believed to depend on their niches, that is, the microenvironment in which these stem cells reside. A similar concept applies to understanding the development of cancer, as it is becoming increasingly clear that only a small subset of cancer cell populations is capable of initiating/sustaining tumor formation. These tumorigenic cells, commonly referred to as cancer stem cells, also appear to reside in particular niches, and they bear the known, albeit dysfunctional, stem cell characteristics of self-renewal and differentiation. Dysregulation of stem cell niches is thought to contribute to tumorigenesis by affecting the complex network of signaling interactions that occur between stem cells and their neighboring cells, thus imbalancing the physiological controls on self-renewal and differentiation processes. This hypothesis was widely explored at the conference to shed new light on the mechanisms of tumor origin and progression and to unveil novel antitumor therapeutic approaches.
Disclosure of potential conflicts of interest is found at the end of this article.

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