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RNA helicase a is a downstream mediator of KIF1Bβ tumor-suppressor function in neuroblastoma

Chen, Z. X. (author)
Ludwig Institute for Cancer Research Ltd., Karolinska Institutet, Nobels väg 3, SE-17177, Stockholm, Sweden
Wallis, K. (author)
Ludwig Institute for Cancer Research Ltd., Karolinska Institutet, Nobels väg 3, SE-17177, Stockholm, Sweden
Fell, S. M. (author)
Karolinska Institutet
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Sobrado, V. R. (author)
Ludwig Institute for Cancer Research Ltd., Karolinska Institutet, Nobels väg 3, SE-17177, Stockholm, Sweden
Hemmer, M. C. (author)
Ludwig Institute for Cancer Research Ltd., Karolinska Institutet, Nobels väg 3, SE-17177, Stockholm, Sweden
Ramsköld, D. (author)
Karolinska Institutet
Hellman, Ulf (author)
Uppsala universitet,Ludwiginstitutet för cancerforskning
Sandberg, R. (author)
Karolinska Institutet
Kenchappa, R. S. (author)
Martinson, Tommy (author)
Gothenburg University,Göteborgs universitet,Institutionen för biomedicin, avdelningen för medicinsk genetik och klinisk genetik,Institute of Biomedicine, Department of Medical and Clinical Genetics,Department of Clinical Genetics, Institute of Biomedicine, University of Gothenburg, Sahlgrenska University Hospital, Göteborg, Sweden
Johnsen, J. I. (author)
Karolinska Institutet
Kogner, P. (author)
Karolinska Institutet
Schlisio, S. (author)
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Karolinska Institutet Ludwig Institute for Cancer Research Ltd, Karolinska Institutet, Nobels väg 3, SE-17177, Stockholm, Sweden (creator_code:org_t)
2014
2014
English.
In: Cancer Discovery. - 2159-8274 .- 2159-8290. ; 4:4, s. 434-451
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • Inherited KIF1B loss-of-function mutations in neuroblastomas and pheochromocytomas implicate the kinesin KIF1B as a 1p36.2 tumor suppressor. However, the mechanism of tumor suppression is unknown. We found that KIF1B isoform β (KIF1Bβ) interacts with RNA helicase A (DHX9), causing nuclear accumulation of DHX9, followed by subsequent induction of the proapoptotic XIAP-associated factor 1 (XAF1) and, consequently, apoptosis. Pheochromocytoma and neuroblastoma arise from neural crest progenitors that compete for growth factors such as nerve growth factor (NGF) during development. KIF1Bβ is required for developmental apoptosis induced by competition for NGF. We show that DHX9 is induced by and required for apoptosis stimulated by NGF deprivation. Moreover, neuroblastomas with chromosomal deletion of 1p36 exhibit loss of KIF1Bβ expression and impaired DHX9 nuclear localization, implicating the loss of DHX9 nuclear activity in neuroblastoma pathogenesis. SIGNIFICANCE: KIF1Bβ has neuroblastoma tumor-suppressor properties and promotes and requires nuclear-localized DHX9 for its apoptotic function by activating XAF1 expression. Loss of KIF1Bβ alters subcellular localization of DHX9 and diminishes NGF dependence of sympathetic neurons, leading to reduced culling of neural progenitors, and, therefore, might predispose to tumor formation.

Subject headings

MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine (hsv//eng)
MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Cancer och onkologi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Cancer and Oncology (hsv//eng)

Keyword

antibody
nerve growth factor
RNA helicase
RNA helicase A
unclassified drug

Publication and Content Type

ref (subject category)
art (subject category)

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