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Keiichiro Honma

Researcher at Niigata University

Publications -  48
Citations -  781

Keiichiro Honma is an academic researcher from Niigata University. The author has contributed to research in topics: Medicine & Internal medicine. The author has an hindex of 8, co-authored 22 publications receiving 654 citations.

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TNFAIP3/A20 functions as a novel tumor suppressor gene in several subtypes of non-Hodgkin lymphomas

TL;DR: The study extended the analysis to other subsets of non-Hodgkin lymphomas and found that A20 is frequently deleted in mantle cell lymphoma and diffuse large B-cell lymphoma, raising the possibility that inactivation of A20 may be involved in lymphomagenesis.
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Identification of FOXO3 and PRDM1 as tumor-suppressor gene candidates in NK-cell neoplasms by genomic and functional analyses

TL;DR: Oligo-array comparative genomic hybridization and gene-expression profiling of natural killer (NK)-cell neoplasms were used in an effort to delineate the molecular pathogenesis involved and identified two 6q21 regions that were most frequently deleted.
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TNFAIP3 is the target gene of chromosome band 6q23.3-q24.1 loss in ocular adnexal marginal zone B cell lymphoma.

TL;DR: It is suggested that TNFAIP3 may act as a tumor suppressor gene in ocular adnexal marginal zone B cell lymphoma and correlation between genomic loss and expression level was found only for TNFAip3, demonstrating that TN FAIP3 is a target gene of 6q deletion in ophthalmological lymphoma.
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Genome-wide array-based comparative genomic hybridization of ocular marginal zone B cell lymphoma: comparison with pulmonary and nodal marginal zone B cell lymphoma.

TL;DR: The array CGH profile of ocular MZ BCL is distinct from those of pulmonary and nodal MZBCL, and deletion of chromosome band 6q23.3 in ocular ZBCL is a novel finding and may constitute a crucial genetic alteration in the pathogenesis of ophthalmology.
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Diversity of genome profiles in malignant lymphoma

TL;DR: The importance of genetic alterations other than chromosome translocation has been recognized since the introduction of array comparative genomic hybridization (array CGH) analyses as mentioned in this paper, which indicate that multiple genetic pathways leading to the development of lymphomas may exist and hence result in the variable clinicopathological features observed.