The presence of the protein KIF1Bbeta can play a central role for the outcome of a neuroblastoma diagnosis
Karolinska Institutet Jun 30, 2017
A high percentage of KIF1B? means a greater chance of the tumour spontaneously regressing and disappearing. These are the results of a study by Karolinska Institutet (KI) and the Ludwig Institute for Cancer Research Ltd.
The study was published in the journal Genes and Development.
Neuroblastoma is the third most common form of childhood cancer and causes almost 15 per cent of all cancer–related deaths in children. This high mortality fully reflects both the aggressive nature of the disease and that it often gives rise to metastases. Paradoxically enough, neuroblastoma also has the highest spontaneous regression frequency of all tumoural diseases.
In the present study, the researchers showed that absence of KIF1Bbeta contributes to normal neuroblasts not maturing into nerve cells and to a more immature neuroblastoma with a poorer prognosis.
ÂOur study shows that unimpaired maturing of neuroblasts is a basic prerequisite for spontaneous regression of neuroblastoma. What is behind this regression is unknown, but our study is an important piece in the jigsaw for understanding the mechanisms that cause this phenomenon. Understanding this process in greater detail can provide clues for the development of new therapies. For example, it would be interesting to increase levels of KIF1Bbeta activity to see if this facilitates, or even induces, tumour regression, comments Susanne Schlisio, researcher at KIÂs Department of Microbiology, Tumor and Cell Biology and at Ludwig Institute for Cancer Research Ltd.
High gene expression of the NGF receptor Trka correlates well with good prognoses and with spontaneous regression of the tumour. Conversely, low levels of Trka, partnered with loss of the 1p36 chromosome locus and amplification of the MYCN oncogene, are associated with poor prognoses. ÂWe have previously shown that the kinesin protein KIF1Bbeta, which is present on chromosome 1p36, is a candidate tumour suppressor and that a low expression is correlated with lower survival of neuroblastoma patients, says Schlisio.
The research is being financed with funding from the Swedish Childhood Cancer Foundation, the Swedish Cancer Society, the Swedish Research Council, the Paradifference Foundation and the Gösta Fraenckel Foundation for Medical Research.
Go to Original
The study was published in the journal Genes and Development.
Neuroblastoma is the third most common form of childhood cancer and causes almost 15 per cent of all cancer–related deaths in children. This high mortality fully reflects both the aggressive nature of the disease and that it often gives rise to metastases. Paradoxically enough, neuroblastoma also has the highest spontaneous regression frequency of all tumoural diseases.
In the present study, the researchers showed that absence of KIF1Bbeta contributes to normal neuroblasts not maturing into nerve cells and to a more immature neuroblastoma with a poorer prognosis.
ÂOur study shows that unimpaired maturing of neuroblasts is a basic prerequisite for spontaneous regression of neuroblastoma. What is behind this regression is unknown, but our study is an important piece in the jigsaw for understanding the mechanisms that cause this phenomenon. Understanding this process in greater detail can provide clues for the development of new therapies. For example, it would be interesting to increase levels of KIF1Bbeta activity to see if this facilitates, or even induces, tumour regression, comments Susanne Schlisio, researcher at KIÂs Department of Microbiology, Tumor and Cell Biology and at Ludwig Institute for Cancer Research Ltd.
High gene expression of the NGF receptor Trka correlates well with good prognoses and with spontaneous regression of the tumour. Conversely, low levels of Trka, partnered with loss of the 1p36 chromosome locus and amplification of the MYCN oncogene, are associated with poor prognoses. ÂWe have previously shown that the kinesin protein KIF1Bbeta, which is present on chromosome 1p36, is a candidate tumour suppressor and that a low expression is correlated with lower survival of neuroblastoma patients, says Schlisio.
The research is being financed with funding from the Swedish Childhood Cancer Foundation, the Swedish Cancer Society, the Swedish Research Council, the Paradifference Foundation and the Gösta Fraenckel Foundation for Medical Research.
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