Gene often lost in childhood cancer crucial in cells' life or death decision

Neuroblastoma is the third most common type of tumour in children. Its aggressive nature and the frequency of metastatic disease at diagnosis contribute to the fact that neuroblastoma accounts for almost 15 per cent of childhood cancer fatalities. For the past two decades a region on chromosome 1 that is often missing in neuroblastoma cells has been thought to harbour an important tumour suppressor gene.

"Our data strongly suggest that KIF1Bβ, which is localised on chromosome 1p36, might be such a neuroblastoma tumour suppressor gene", says principal investigator Susanne Schlisio at the Department of Microbiology, Tumor and Cell Biology at Karolinska Institutet and Assistant Member at the Ludwig Institute for Cancer Research in Stockholm, Sweden.

Neuroblastoma tumours originate from the same transient progenitor cells——that give rise to the nervous system along with other tissues. Members of some families are at higher risk than others to develop tumours that originate from these cells due to mutations in specific genes. The research team behind the new study previously discovered that genes mutated in some of the tumours play a central role in determining whether neural crest cells live or die. Neural crest cells that should ordinarily have succumbed to programmed escape that fate when KIF1B-β is lost. Later in life, the cells might develop into .

In the current study, the investigators describe the mechanisms by which KIF1B-β causes cell death. They found that KIF1B-β affects the cells´ power stations, the mitochondria, by activating an enzyme named calcineurin. Schlisio and her colleagues also show that a critical signal required to induce cell death by fragmenting the mitochondria is compromised by the loss of KIF1B-β. By examining neuroblastoma tumors biopsied from patients, the researchers demonstrate that loss of KIF1B-β is associated with poor prognosis and reduced survival.

The team also demonstrates a general mechanism that can explain how calcium-dependent signalling by calcineurin is executed. This is a significant finding because the loss of control of calcineurin signalling seems to play a role in many diseases, including neurodegenerative disease, cardiac disease and cancers.

"We conclude that KIF1B-β plays a key role in the decision between life and death for neural and tumours originating from the ", says Susanne Schlisio. "In time, knowledge of the mechanism by which KIF1B-β induce cell death might prove important in attempts to develop new neuroblastoma therapies."


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More information: 'The 1p36 tumor suppressor KIF 1Bβ is required for Calcineurin activation controlling mitochondrial fission and apoptosis', Shuijie Li, Stuart M Fell, Olga Surova, Erik Smedler, Zhi Xiong Chen, Ulf Hellman, John Inge Johnsen, Tommy Martinsson, Rajappa Kenchappa, Per Uhlén, Per Kogner and Susanne Schlisio, Developmental Cell, online Jan. 25 2016,DOI: 10.1016/j.devcel.2015.12.029
Journal information: Developmental Cell

Citation: Gene often lost in childhood cancer crucial in cells' life or death decision (2016, January 25) retrieved 26 January 2021 from https://medicalxpress.com/news/2016-01-gene-lost-childhood-cancer-crucial.html
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