Abstract/Details

The Roles of Ras and Neurofibromin 1 in Human Neuroblastoma Stem Cell Malignancy


2011 2011

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Abstract (summary)

Cancer stem or tumor-initiating cells are present in many human cancers. However, the molecular mechanisms responsible for the clinical aggressiveness of these cells are still unclear. Human neuroblastoma, originating from the embryonic neural crest, is characterized by cellular heterogeneity. Cells of three phenotypes (N-, I-, and S-type) have been isolated and characterized. Among these, the I-type cell – the cancer stem cell of neuroblastoma – is the most malignant.

In the present study, I show that, although wild-type N-Ras protein is expressed at similar levels in all three neuroblastoma cell phenotypes, a significantly higher level of activation (>5-fold) is restricted to I-type cancer stem cells. To study the role of activated N-Ras in neuroblastoma cell malignancy, Ras-GTP levels were altered using dominant-negative (DN) or constitutively active (CA) N-Ras constructs. DN-N-Ras transfection led to >2-fold decrease in Ras-GTP levels in two I-type cell lines and caused a significant >3-fold decrease in their colony-forming efficiency (CFE) in soft agar. Conversely, when weakly malignant N-type cells were transfected with CA-N-Ras, Ras-GTP levels increased >10-fold and this was accompanied by a significant >7-fold increased CFE. Moreover, in cell survival studies, high level of Ras-GTP was shown to protect neuroblastoma cells from apoptosis. Thus, high level of N-Ras-GTP promotes the increased malignancy and survival of I-type neuroblastoma cancer stem cells.

To reveal the possible mechanisms underlying the enhanced Ras activation found in neuroblastoma cancer stem cells, I showed that one important Ras-GTPase activating protein, neurofibromin, was specifically down-regulated (>3-fold) in I-type cells. To assess whether lower neurofibromin content directly results in elevated Ras activation, NF1-specific shRNA was expressed in N-type cells, leading to a significant >2-fold decrease in neurofibromin amount and a >3-fold increase in Ras-GTP level. Moreover, these cells showed significant >2-fold increases in CFE. These results suggest that high level of Ras-GTP - as a consequence of low amount of neurofibromin - is a cancer stem cell-specific property in neuroblastoma, and is instrumental in their malignancy. Furthermore, a MG132 study showed that the I-type cell-specific down-regulation of neurofibromin is due to increased ubiquitin-proteasome-dependent degradation of neurofibromin protein.

These findings are the first to implicate wild-type N-Ras and neurofibromin in the malignancy of human neuroblastoma and to identify a cancer stem cell-specific regulatory mechanism underlying their highly malignant behavior. These findings may make possible new directions for future therapeutic treatment of this often fatal childhood cancer.

Indexing (details)


Subject
Molecular biology;
Cellular biology;
Oncology
Classification
0307: Molecular biology
0379: Cellular biology
0992: Oncology
Identifier / keyword
Health and environmental sciences; Biological sciences; Cancer stem cells; Malignancy; N-Ras; Neuroblastoma; Neurofibromin
Title
The Roles of Ras and Neurofibromin 1 in Human Neuroblastoma Stem Cell Malignancy
Author
Han, Dan
Number of pages
98
Publication year
2011
Degree date
2011
School code
0072
Source
DAI-B 73/06, Dissertation Abstracts International
Place of publication
Ann Arbor
Country of publication
United States
ISBN
9781267198648
Advisor
Ross, Robert A.
Committee member
Dubrovsky, Edward B.; Rubin, Berish Y.; Thornhill, William B.
University/institution
Fordham University
Department
Biological Sciences
University location
United States -- New York
Degree
Ph.D.
Source type
Dissertations & Theses
Language
English
Document type
Dissertation/Thesis
Dissertation/thesis number
3495890
ProQuest document ID
924343936
Copyright
Database copyright ProQuest LLC; ProQuest does not claim copyright in the individual underlying works.
Document URL
http://search.proquest.com/docview/924343936
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