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Transcriptional networks in neuroblastoma and breast cancer

Manetopoulos, Christina LU (2007) In Lund University Faculty of Medicine Doctoral Dissertation Series 2007:4.
Abstract
Transcription factors of the basic Helix-loop-helix (bHLH) family of proteins are important regulators of cellular processes such as proliferation and differentiation. Many cancer diseases show a block in differentiation, and aberrant regulation of several bHLH factors have been implicated in the development of different malignancies.



Neuroblastoma is a childhood tumour that arises in the developing sympathetic nervous system. The cells are blocked at an early stage of differentiation and display an immature phenotype. HEN1 is a bHLH transcription factor important for neuronal development originally isolated from neuroblastoma. We studied HEN1 and its functional interaction with the Lim-only (LMO) proteins in... (More)
Transcription factors of the basic Helix-loop-helix (bHLH) family of proteins are important regulators of cellular processes such as proliferation and differentiation. Many cancer diseases show a block in differentiation, and aberrant regulation of several bHLH factors have been implicated in the development of different malignancies.



Neuroblastoma is a childhood tumour that arises in the developing sympathetic nervous system. The cells are blocked at an early stage of differentiation and display an immature phenotype. HEN1 is a bHLH transcription factor important for neuronal development originally isolated from neuroblastoma. We studied HEN1 and its functional interaction with the Lim-only (LMO) proteins in neuroblastoma. We detected a strong interaction between HEN1 and LMO4, and this interaction modulated the HEN1 transcription activity. Furthermore, we found a possible role for HEN1 in neuronal differentiation, however, the significance of this finding needs further experiments.



The O/E-protein family also share the HLH motif and functions in neuronal development. In our study on O/E-proteins, we discovered expression of these factors in neuroblastoma. We found that O/E-1 regulate the expression of the important neuronal marker genes SCG10 and Chromogranin A.



bHLH factors are also involved in the regulation of proper development of breast tissue. ID2 has been implicated in the development of breast cancer. We studied the ID2 expression in a breast cancer tissue array, where ID2 correlated with a less aggressive tumour phenotype.



Furthermore, we studied the relation between the important signalling pathways involving Notch1 and its target gene and ERK1/2 in breast cancer. The results revealed a Notch1-independent regulation of Hes1 and that ERK1/2 signalling might contribute to regulation of Hes1 expression in breast cancer. (Less)
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author
supervisor
opponent
  • Professor Åman, Pierre, Department of Pathology, Gothenburg University, Sahlgrenska University Hospital, Sweden
organization
publishing date
type
Thesis
publication status
published
subject
keywords
Medicin (människa och djur), Medicine (human and vertebrates), basic helix-loop-helix, Neuroblastoma, Breast cancer
in
Lund University Faculty of Medicine Doctoral Dissertation Series
volume
2007:4
pages
102 pages
publisher
Department of Laboratory Medicine, Lund University
defense location
Entrance 78, 2nd floor, Pathology lecture hall University Hospital MAS, Malmö
defense date
2007-01-18 09:15:00
ISSN
1652-8220
ISBN
91-85559-74-1
language
English
LU publication?
yes
additional info
id
6c38a779-673e-4399-b312-9e4b3b6f162e (old id 547842)
date added to LUP
2016-04-01 16:27:37
date last changed
2019-05-21 22:16:45
@phdthesis{6c38a779-673e-4399-b312-9e4b3b6f162e,
  abstract     = {{Transcription factors of the basic Helix-loop-helix (bHLH) family of proteins are important regulators of cellular processes such as proliferation and differentiation. Many cancer diseases show a block in differentiation, and aberrant regulation of several bHLH factors have been implicated in the development of different malignancies.<br/><br>
<br/><br>
Neuroblastoma is a childhood tumour that arises in the developing sympathetic nervous system. The cells are blocked at an early stage of differentiation and display an immature phenotype. HEN1 is a bHLH transcription factor important for neuronal development originally isolated from neuroblastoma. We studied HEN1 and its functional interaction with the Lim-only (LMO) proteins in neuroblastoma. We detected a strong interaction between HEN1 and LMO4, and this interaction modulated the HEN1 transcription activity. Furthermore, we found a possible role for HEN1 in neuronal differentiation, however, the significance of this finding needs further experiments.<br/><br>
<br/><br>
The O/E-protein family also share the HLH motif and functions in neuronal development. In our study on O/E-proteins, we discovered expression of these factors in neuroblastoma. We found that O/E-1 regulate the expression of the important neuronal marker genes SCG10 and Chromogranin A.<br/><br>
<br/><br>
bHLH factors are also involved in the regulation of proper development of breast tissue. ID2 has been implicated in the development of breast cancer. We studied the ID2 expression in a breast cancer tissue array, where ID2 correlated with a less aggressive tumour phenotype.<br/><br>
<br/><br>
Furthermore, we studied the relation between the important signalling pathways involving Notch1 and its target gene and ERK1/2 in breast cancer. The results revealed a Notch1-independent regulation of Hes1 and that ERK1/2 signalling might contribute to regulation of Hes1 expression in breast cancer.}},
  author       = {{Manetopoulos, Christina}},
  isbn         = {{91-85559-74-1}},
  issn         = {{1652-8220}},
  keywords     = {{Medicin (människa och djur); Medicine (human and vertebrates); basic helix-loop-helix; Neuroblastoma; Breast cancer}},
  language     = {{eng}},
  publisher    = {{Department of Laboratory Medicine, Lund University}},
  school       = {{Lund University}},
  series       = {{Lund University Faculty of Medicine Doctoral Dissertation Series}},
  title        = {{Transcriptional networks in neuroblastoma and breast cancer}},
  volume       = {{2007:4}},
  year         = {{2007}},
}