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2018 Fiscal Year Final Research Report

The role of the nucleic acid sensor molecule DHX29 in hematopoietic cell immune responses and hematopoietic tumors

Research Project

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Project/Area Number 15K09500
Research Category

Grant-in-Aid for Scientific Research (C)

Allocation TypeMulti-year Fund
Section一般
Research Field Hematology
Research InstitutionKagawa University (2017-2018)
Kyoto University (2015-2016)

Principal Investigator

Sugimoto Naoshi  香川大学, 医学部附属病院, 助教 (10447956)

Research Collaborator Kadowaki Norimitsu  
Kawahara Masahiro  
Project Period (FY) 2015-04-01 – 2019-03-31
KeywordsDHX29 / DDX41 / 造血器腫瘍 / 細胞内核酸センサー / eIF4E / eIF4GI
Outline of Final Research Achievements

The expression of DHX29 was not observed in fresh peripheral blood subsets, but induced in differentiated monocytes and activated T, B and NK cells. DHX29 was highly expressed in all 10 of various hematopoietic cell lines and in 4 out 6 blood samples of patients with hematological malignancies. Knockdown of DHX29 showed no apparent effect in cell proliferation and immune responses, but 4EGI-1, an inhibitor of eIF4E/eIF4F which cooperate with DHX29, significantly suppressed the proliferation and downregulated the expression of c-MYC. These results suggest that DHX29 contributes to tumorigenesis of hematological malignancies through cooperation with other translation relates proteins to endow tumor growth advantage.

Free Research Field

血液内科学

Academic Significance and Societal Importance of the Research Achievements

DExD/Hヘリカーゼ・ファミリー分子に属するDHX29やDDX41は、mRNAの翻訳や腫瘍細胞の生存・ 増殖、細胞質内のウィルス・核酸センサーとして働いている。DDX41は急性骨髄性白血病の病態発生に関与し、DHX29もeIF4E/eIF4Fと協調して癌細胞で働いていると報告されているが、今回の研究によりDHX29およびeIF4E/eIF4Fは造血器腫瘍の病態にも関与していることが示唆される結果が得られ、今後造血器悪性疾患の新たな治療標的となると見込まれる。

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Published: 2020-03-30  

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