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Inherited and Somatic Defects in DDX41 in Myeloid Neoplasms.


ABSTRACT: Most cases of adult myeloid neoplasms are routinely assumed to be sporadic. Here, we describe an adult familial acute myeloid leukemia (AML) syndrome caused by germline mutations in the DEAD/H-box helicase gene DDX41. DDX41 was also found to be affected by somatic mutations in sporadic cases of myeloid neoplasms as well as in a biallelic fashion in 50% of patients with germline DDX41 mutations. Moreover, corresponding deletions on 5q35.3 present in 6% of cases led to haploinsufficient DDX41 expression. DDX41 lesions caused altered pre-mRNA splicing and RNA processing. DDX41 is exemplary of other RNA helicase genes also affected by somatic mutations, suggesting that they constitute a family of tumor suppressor genes.

SUBMITTER: Polprasert C 

PROVIDER: S-EPMC8713504 | biostudies-literature | 2015 May

REPOSITORIES: biostudies-literature

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Inherited and Somatic Defects in DDX41 in Myeloid Neoplasms.

Polprasert Chantana C   Schulze Isabell I   Sekeres Mikkael A MA   Makishima Hideki H   Przychodzen Bartlomiej B   Hosono Naoko N   Singh Jarnail J   Padgett Richard A RA   Gu Xiaorong X   Phillips James G JG   Clemente Michael M   Parker Yvonne Y   Lindner Daniel D   Dienes Brittney B   Jankowsky Eckhard E   Saunthararajah Yogen Y   Du Yang Y   Oakley Kevin K   Nguyen Nhu N   Mukherjee Sudipto S   Pabst Caroline C   Godley Lucy A LA   Churpek Jane E JE   Pollyea Daniel A DA   Krug Utz U   Berdel Wolfgang E WE   Klein Hans-Ulrich HU   Dugas Martin M   Shiraishi Yuichi Y   Chiba Kenichi K   Tanaka Hiroko H   Miyano Satoru S   Yoshida Kenichi K   Ogawa Seishi S   Müller-Tidow Carsten C   Maciejewski Jaroslaw P JP  

Cancer cell 20150423 5


Most cases of adult myeloid neoplasms are routinely assumed to be sporadic. Here, we describe an adult familial acute myeloid leukemia (AML) syndrome caused by germline mutations in the DEAD/H-box helicase gene DDX41. DDX41 was also found to be affected by somatic mutations in sporadic cases of myeloid neoplasms as well as in a biallelic fashion in 50% of patients with germline DDX41 mutations. Moreover, corresponding deletions on 5q35.3 present in 6% of cases led to haploinsufficient DDX41 expr  ...[more]

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