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Telomerase Inhibition Targets Clonogenic Multiple Myeloma Cells through Telomere Length-Dependent and Independent Mechanisms

Overview of attention for article published in PLOS ONE, September 2010
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Title
Telomerase Inhibition Targets Clonogenic Multiple Myeloma Cells through Telomere Length-Dependent and Independent Mechanisms
Published in
PLOS ONE, September 2010
DOI 10.1371/journal.pone.0012487
Pubmed ID
Authors

Sarah K. Brennan, Qiuju Wang, Robert Tressler, Calvin Harley, Ning Go, Ekaterina Bassett, Carol Ann Huff, Richard J. Jones, William Matsui

Abstract

Plasma cells constitute the majority of tumor cells in multiple myeloma (MM) but lack the potential for sustained clonogenic growth. In contrast, clonotypic B cells can engraft and recapitulate disease in immunodeficient mice suggesting they serve as the MM cancer stem cell (CSC). These tumor initiating B cells also share functional features with normal stem cells such as drug resistance and self-renewal potential. Therefore, the cellular processes that regulate normal stem cells may serve as therapeutic targets in MM. Telomerase activity is required for the maintenance of normal adult stem cells, and we examined the activity of the telomerase inhibitor imetelstat against MM CSC. Moreover, we carried out both long and short-term inhibition studies to examine telomere length-dependent and independent activities.

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Geographical breakdown

Country Count As %
United States 1 2%
Germany 1 2%
Belgium 1 2%
Unknown 47 94%

Demographic breakdown

Readers by professional status Count As %
Researcher 11 22%
Student > Ph. D. Student 10 20%
Student > Bachelor 5 10%
Other 5 10%
Professor > Associate Professor 5 10%
Other 9 18%
Unknown 5 10%
Readers by discipline Count As %
Medicine and Dentistry 17 34%
Agricultural and Biological Sciences 17 34%
Biochemistry, Genetics and Molecular Biology 4 8%
Immunology and Microbiology 1 2%
Philosophy 1 2%
Other 4 8%
Unknown 6 12%