Gene Often Lost in Childhood Cancer Crucial in Cells’ Life or Death Decision

"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—neural crest 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 cell death escape that fate when KIF1B-β is lost. Later in life, the cells might develop into cancer cells.

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 crest cells and tumours originating from the neural crest", 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."

The research was financially supported by grants from the Ludwig Institute, the Swedish Children Cancer Foundation, the Swedish Research Council (VR) and the Swedish Cancer Society.

Publication: '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 January 25 2016,DOI:10.1016/j.devcel.2015.12.029


About Ludwig Cancer Research

Ludwig Cancer Research is an international collaborative network of acclaimed scientists that has pioneered cancer research and landmark discovery for more than 40 years. Ludwig combines basic science with the ability to translate its discoveries and conduct clinical trials to accelerate the development of new cancer diagnostics and therapies. Since 1971, Ludwig has invested nearly $2.7 billion in life-changing science through the not-for-profit Ludwig Institute for Cancer Research and the six U.S.-based Ludwig Centers. To learn more, visit www.ludwigcancerresearch.org.

About Karolinska Institutet

Karolinska Institutet is one of the world's leading medical universities. Its vision is to significantly contribute to the improvement of human health. Karolinska Institutet accounts for over 40 per cent of the medical academic research conducted in Sweden and offers the country´s broadest range of education in medicine and health sciences. The Nobel Assembly at Karolinska Institutet selects the Nobel laureates in Physiology or Medicine.

For further information please contact:

Rachel SteinhardtVice President of Communications, Ludwig Institute for Cancer Research[email protected] or +1-212-450-1582.

Karolinska Institutet Press Officehttp://ki.se/pressroom [email protected] or +46 (0)8524 860 77