2016 Fiscal Year Annual Research Report
大規模シーケンスとコンピューティングによるがんの進化と多様性の解明
Project Area | Conquering cancer through neo-dimensional systems understanding |
Project/Area Number |
15H05909
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Research Institution | Kyoto University |
Principal Investigator |
小川 誠司 京都大学, 医学研究科, 教授 (60292900)
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Project Period (FY) |
2015-06-29 – 2020-03-31
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Keywords | 総合生物 / ゲノム科学 / システムゲノム科学 / 腫瘍学 |
Outline of Annual Research Achievements |
a)癌の起源と進化に関する解析。骨髄異形成症候群について、2500例を超えるMDSの遺伝子変異について、MDSの病期に集積する特徴的な変異を明らかにするとともに、100例を超える経時的な試料の解析によりそれらの病期進行における意義を明らかにした(牧島ら、Nature Genetics, 2017他)。また、大腸および尿管上皮の前がん病変の解析から、大腸がん、腎盂尿管がんの初期病変に関わる遺伝子変異と、これらの変異を生じたクローンが拡大する様式を明らかにした。 b)全ゲノムシーケンスによる新たな発がんメカニズムの解析については、成人T細胞白血病(ATL)の全ゲノムシーケンスの解析により、ATLの約25%の症例で、免疫チェックポイントの一つである PD-L1遺伝子の3’非翻訳領域(3’-UTR)に様々な構造異常が生じ、PD-L1の著しい発現上昇が惹起されることが明らかとなった。さらに、京コンピュータ等を駆使した10000例を超えるがんのRNAシーケンスデータの解析から、同様の異常が様々な癌腫で認められたことから、PD-L1の構造異常を介した免疫回避がヒトのがんで重要な役割を担っていることが示唆された(片岡ら、Nature, 2016)。また、これらの異常を有する腫瘍は、ニボルマブを初めとする抗PD-1抗体が有効である可能性が示唆された。 c)胚細胞系列の変異に関する解析については、DDX41遺伝子のマウスモデルの解析を進めるとともに、日本バイオバンクの1万例を超える健常試料に関する標的シーケンスを行った。 d)臨床シーケンスについては、日本骨髄バンクを通じて非血縁移植が行われたMDS症例約800例について、骨髄系腫瘍で高頻度に変異する遺伝子に関する網羅的な標的シーケンスを行い、遺伝子変異が移植成績に及ぼす効果を明らかにした(吉里ら、Blood, 2017)。
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Current Status of Research Progress |
Current Status of Research Progress
1: Research has progressed more than it was originally planned.
Reason
ATLの全ゲノムシーケンス解析では、がんの免疫回避に関わる主要分子であるPD-L1の3’UTRを含む構造異常がATLを初めとする様々なヒトのがんで認められ、がんの免疫回避に関わっていること、またPD-L1の3’UTRが同遺伝子の発現調節に重要な役割を担っていることを世界で初めて明らかにした。本研究成果は、2016年、Nature紙に掲載され(片岡ら、Nature, 2016)、抗腫瘍免疫に関わる顕著な発見として国際的に極めて高く評価されており、文部科学大臣表彰の栄に浴することができた。 一方、骨髄異形成症候群(MDS)の発症と進展に関わる研究においては、2500例のMDSにおける遺伝子変異に関する検討から、MDSの病期の進展と遺伝子変異の関係に関する網羅的な検討を行うとともに、経時的に採取されたMDS試料の全エクソン・標的シーケンスを行うことにより、MDSの病期の進展・クローン進化に関わる遺伝子変異とその意義を明らかにした。本研究は、Nature genetics紙およびNature communication紙に掲載され、MDSの病態解明のみならず、MDSの予後予測や治療判断の決定における臨床シーケンスの有用性を示す研究成果として高く評価されている(牧島ら、Nature genetics, 2017および、de Silva-Coelho et al., Nature comm, 2016)。さらに、日本骨髄バンクにおける800例を超える移植症例の遺伝子変異の解析から、MDSの造血幹細胞移植における遺伝子変異の効果の検討について明らかにし (吉里ら、Blood, 2017)、MDSの研究分野で高い評価を受けている。 その他、大腸がん、食道がんその他の解析についても、大旨予定どおりに進行しており、また以上の成果に鑑みて、研究は当初の予定以上の研究成果が得られていると判断した。
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Strategy for Future Research Activity |
1)癌の起源と進化に関する解析では、食道癌、大腸がん、甲状腺癌および泌尿器系腫瘍について、前がん病変、健常組織を含めた多数サンプリングによるシーケンス解析をさらに進めることにより、これらのがんの発症とクローン進化の過程をその初期病変から解明することを試みる。 2)全ゲノムシーケンスによる新たな発がんメカニズムの解析。びまん性大細胞型リンパ腫、中枢神経リンパ腫、末梢T細胞性リンパ腫、およびMDSについて腫瘍および正常組織(頬粘膜ないしCD3陽性細胞)についも、各48ペアについて全ゲノムシーケンス解析を行い、宮野らによる新規アルゴリズムを用いて単一塩基置換、塩基の挿入欠失、tandem duplication、遺伝子再構成を高精度に同定する。また、non-coding RNAの発現異常や構造異常に関わるゲノム変異を同定し、同定されたnon-coding RNAについては、癌化における意義について機能的な解析を行う。 3)胚細胞系列の変異に関する解析。家族性MDSの家系について全エクソンないし全ゲノムシーケンスを行い、MDSの発症に関わる胚細胞変異の同定を試みる。DDX41遺伝子変異については前年度までに作成した機能欠失アレルおよびR525Hアレルを導入したマウスモデルにおける経時的採血によって得られる試料のシーケンス解析を用いたMDSのクローン進化の検討を行う。Biobabk Japanの試料を用いた次世代シーケンス解析により、骨髄系腫瘍におけるドライバー遺伝子の胚細胞変異の網羅的な探索を行う。 4)臨床シーケンスに関する検討。大腸癌検体1000例および甲状腺乳頭癌500例について既知のドライバー変異に関するターゲットシーケンスを行い、遠隔転移や予後と相関する分子マーカーの同定を行う。
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Research Products
(106 results)
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[Journal Article] Recurrent genetic defects on chromosome 5q in myeloid neoplasms.2017
Author(s)
Hosono N, Makishima H, Mahfouz R, Przychodzen B, Yoshida K, Jerez A, LaFramboise T, Polprasert C, Clemente MJ, Shiraishi Y, Chiba K, Tanaka H, Miyano S, Sanada M, Cui E, Verma AK, McDevitt MA, List AF, Saunthararajah Y, Sekeres MA, Boultwood J, Ogawa S, Maciejewski JP.
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Journal Title
Oncotarget.
Volume: 8
Pages: 6483-6495
DOI
Peer Reviewed / Int'l Joint Research / Acknowledgement Compliant
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[Journal Article] ASXL2 Mutations are Frequently Found in Pediatric AML Patients with t(8;21)/RUNX1-RUNX1T1 and Associated with a Better Prognosis.2017
Author(s)
Yamato G, Shiba N, Yoshida K, Shiraishi Y, Hara Y, Ohki K, Okubo J, Okuno H, Chiba K, Tanaka H, Kinoshita A, Moritake H, Kiyokawa N, Tomizawa D, Park MJ, Sotomatsu M, Taga T, Adachi S, Tawa A, Horibe K, Arakawa H, Miyano S, Ogawa S, Hayashi Y.
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Journal Title
Genes Chromosomes Cancer.
Volume: -
Pages: -
DOI
Peer Reviewed / Acknowledgement Compliant
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[Journal Article] Haploinsufficiency of TNFAIP3 (A20) by germline mutation is involved in autoimmune lymphoproliferative syndrome.2017
Author(s)
Takagi M, Ogata S, Ueno H, Yoshida K, Yeh T, Hoshino A, Piao J, Yamashita M, Nanya M, Okano T, Kajiwara M, Kanegane H, Muramatsu H, Okuno Y, Shiraishi Y, Chiba K, Tanaka H, Bando Y, Kato M, Hayashi Y, Miyano S, Imai K, Ogawa S, Kojima S, Morio T.
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Journal Title
J Allergy Clin Immunol.
Volume: -
Pages: -
DOI
Peer Reviewed / Acknowledgement Compliant
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[Journal Article] BRCA1 Alterations with Additional Defects in DNA Damage Response Genes May Confer Chemoresistance to BRCA-like Breast Cancers Treated with Neoadjuvant Chemotherapy.2017
Author(s)
Takada M, Nagai S, Haruta M, Sugino RP, Tozuka K, Takei H, Ohkubo F, Inoue K, Kurosumi M, Miyazaki M, Sato-Otsubo A, Sato Y, Ogawa S, Kaneko Y.
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Journal Title
Genes Chromosomes Cancer.
Volume: -
Pages: -
DOI
Peer Reviewed / Acknowledgement Compliant
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[Journal Article] Ordering of mutations in acute myeloid leukemia with partial tandem duplication of MLL (MLL-PTD).2017
Author(s)
Sun QY, Ding LW, Tan KT, Chien W, Mayakonda A, Lin DC, Loh XY, Xiao JF, Meggendorfer M, Alpermann T, Garg M, Lim SL, Madan V, Hattori N, Nagata Y, Miyano S, Yeoh AE, Hou HA, Jiang YY, Takao S, Liu LZ, Tan SZ, Lill M, Hayashi M, Kinoshita A, Kantarjian HM, Kornblau SM, Ogawa S, Haferlach T, Yang H, Koeffler HP.
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Journal Title
Leukemia.
Volume: 31
Pages: 1-10
DOI
Int'l Joint Research
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[Journal Article] Partial monosomy of 10p and duplication of another chromosome in two patients.2017
Author(s)
Ohta S, Isojima T, Mizuno Y, Kato M, Mimaki M, Seki M, Sato Y, Ogawa S, Takita J, Kitanaka S, Oka A.
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Journal Title
Pediatr Int.
Volume: 59
Pages: 99-102
DOI
Peer Reviewed / Acknowledgement Compliant
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[Journal Article] Structural Determinants of the Gain-of-Function Phenotype of Human Leukemia-associated Mutant CBL Oncogene.2017
Author(s)
Nadeau SA, An W, Mohapatra BC, Mushtaq I, Bielecki TA, Luan H, Zutshi N, Ahmad G, Storck MD, Sanada M, Ogawa S, Band V, Band H.
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Journal Title
J Biol Chem.
Volume: -
Pages: -
Peer Reviewed
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[Journal Article] Clinical utility of next-generation sequencing for inherited bone marrow failure syndromes.2017
Author(s)
Muramatsu H, Okuno Y, Yoshida K, Shiraishi Y, Doisaki S, Narita A, Sakaguchi H, Kawashima N, Wang X, Xu Y, Chiba K, Tanaka H, Hama A, Sanada M, Takahashi Y, Kanno H, Yamaguchi H, Ohga S, Manabe A, Harigae H, Kunishima S, Ishii E, Kobayashi M, Koike K, Watanabe K, Ito E, Takata M, Yabe M, Ogawa S, Miyano S, Kojima S.
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Journal Title
Genet Med.
Volume: -
Pages: -
DOI
Peer Reviewed / Acknowledgement Compliant
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[Journal Article] Exome sequencing identified RPS15A as a novel causative gene for Diamond-Blackfan anemia.2017
Author(s)
Ikeda F, Yoshida K, Toki T, Uechi T, Ishida S, Nakajima Y, Sasahara Y, Okuno Y, Kanezaki R, Terui K, Kamio T, Kobayashi A, Fujita T, Sato-Otsubo A, Shiraishi Y, Tanaka H, Chiba K, Muramatsu H, Kanno H, Ohga S, Ohara A, Kojima S, Kenmochi N, Miyano S, Ogawa S, Ito E.
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Journal Title
Haematologica.
Volume: -
Pages: -
DOI
Peer Reviewed / Acknowledgement Compliant
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[Journal Article] Diagnostic challenge of Diamond-Blackfan anemia in mothers and children by whole-exome sequencing.2017
Author(s)
Ichimura T, Yoshida K, Okuno Y, Yujiri T, Nagai K, Nishi M, Shiraishi Y, Ueno H, Toki T, Chiba K, Tanaka H, Muramatsu H, Hara T, Kanno H, Kojima S, Miyano S, Ito E, Ogawa S, Ohga S.
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Journal Title
Int J Hematol.
Volume: -
Pages: -
DOI
Peer Reviewed / Acknowledgement Compliant
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[Journal Article] Abnormal hematopoiesis and autoimmunity in human subjects with germline IKZF1 mutations.2017
Author(s)
Hoshino A, Okada S, Yoshida K, Nishida N, Okuno Y, Ueno H, Yamashita M, Okano T, Tsumura M, Nishimura S, Sakata S, Kobayashi M, Nakamura H, Kamizono J, Mitsui-Sekinaka K, Ichimura T, Ohga S, Nakazawa Y, Takagi M, Imai K, Shiraishi Y, Chiba K, Tanaka H, Miyano S, Ogawa S, Kojima S, Nonoyama S, Morio T, Kanegane H.
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Journal Title
J Allergy Clin Immunol.
Volume: -
Pages: -
DOI
Peer Reviewed / Acknowledgement Compliant
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[Journal Article] Mutational Landscape of Pediatric Acute Lymphoblastic Leukemia.2017
Author(s)
Ding LW, Sun QY, Tan KT, Chien W, Thippeswamy AM, Eng Juh Yeoh A, Kawamata N, Nagata Y, Xiao JF, Loh XY, Lin DC, Garg M, Jiang YY, Xu L, Lim SL, Liu LZ, Madan V, Sanada M, Fernandez LT, Preethi H, Lill M, Kantarjian HM, Kornblau SM, Miyano S, Liang DC, Ogawa S, Shih LY, Yang H, Koeffler HP.
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Journal Title
Cancer Res.
Volume: 77
Pages: 390-400
DOI
Peer Reviewed / Acknowledgement Compliant
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[Journal Article] Diagnosis and relapse: cytogenetically normal acute myelogenous leukemia without FLT3-ITD or MLL-PTD.2017
Author(s)
Chien W, Sun QY, Ding LW, Mayakonda A, Takao S, Liu L, Lim SL, Tan KT, Garg M, De Sousa Maria Varela A, Xiao J, Jacob N, Behrens K, Stocking C, Lill M, Madan V, Hattori N, Gery S, Ogawa S, Wakita S, Ikezoe T, Shih LY, Alpermann T, Haferlach T, Yang H, Koeffler HP.
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Journal Title
Leukemia.
Volume: -
Pages: -
DOI
Peer Reviewed / Acknowledgement Compliant
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[Journal Article] The phenotype and clinical course of Japanese Fanconi Anaemia infants is influenced by patient, but not maternal ALDH2 genotype.2016
Author(s)
Yabe M, Yabe H, Morimoto T, Fukumura A, Ohtsubo K, Koike T, Yoshida K, Ogawa S, Ito E, Okuno Y, Muramatsu H, Kojima S, Matsuo K, Hira A, Takata M.
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Journal Title
Br J Haematol.
Volume: 175
Pages: 457-461
DOI
Peer Reviewed / Acknowledgement Compliant
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[Journal Article] Array CGH identifies copy number changes in 11% of 520 MDS patients with normal karyotype and uncovers prognostically relevant deletions.2016
Author(s)
Volkert S, Haferlach T, Holzwarth J, Zenger M, Kern W, Staller M, Nagata Y, Yoshida K, Ogawa S, Schnittger S, Haferlach C.
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Journal Title
Leukemia.
Volume: 30
Pages: 259-261
DOI
Peer Reviewed / Acknowledgement Compliant
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[Journal Article] Paroxysmal nocturnal hemoglobinuria induced by the occurrence of BCR-ABL in a PIGA mutant hematopoietic progenitor cell.2016
Author(s)
Tominaga R, Katagiri T, Kataoka K, Kataoka K, Wee RK, Maeda A, Gomyo H, Mizuno I, Murayama T, Ogawa S, Nakao S.
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Journal Title
Leukemia.
Volume: 30
Pages: 1208-1210
DOI
Peer Reviewed / Open Access / Acknowledgement Compliant
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[Journal Article] Whole-exome sequencing reveals the spectrum of gene mutations and the clonal evolution patterns in paediatric acute myeloid leukaemia.2016
Author(s)
Shiba N, Yoshida K, Shiraishi Y, Okuno Y, Yamato G, Hara Y, Nagata Y, Chiba K, Tanaka H, Terui K, Kato M, Park MJ, Ohki K, Shimada A, Takita J, Tomizawa D, Kudo K, Arakawa H, Adachi S, Taga T, Tawa A, Ito E, Horibe K, Sanada M, Miyano S, Ogawa S, Hayashi Y.
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Journal Title
Br J Haematol.
Volume: 175
Pages: 476-489
DOI
Peer Reviewed / Open Access / Acknowledgement Compliant
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[Journal Article] Genetic basis of myeloid transformation in familial platelet disorder/acute myeloid leukemia patients with haploinsufficient RUNX1 allele.2016
Author(s)
Sakurai M, Kasahara H, Yoshida K, Yoshimi A, Kunimoto H, Watanabe N, Shiraishi Y, Chiba K, Tanaka H, Harada Y, Harada H, Kawakita T, Kurokawa M, Miyano S, Takahashi S, Ogawa S, Okamoto S, Nakajima H.
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Journal Title
Blood Cancer J.
Volume: 6
Pages: e392
DOI
Peer Reviewed / Open Access
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[Journal Article] Impact of SNP array karyotyping on the diagnosis and the outcome of chronic myelomonocytic leukemia with low risk cytogenetic features or no metaphases.2016
Author(s)
Palomo L, Xicoy B, Garcia O, Mallo M, Adema V, Cabezon M, Arnan M, Pomares H, Jose Larrayoz M, Jose Calasanz M, Maciejewski JP, Huang D, Shih LY, Ogawa S, Cervera J, Such E, Coll R, Grau J, Sole F, Zamora L.
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Journal Title
Am J Hematol.
Volume: 91
Pages: 185-192
Peer Reviewed / Open Access
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[Journal Article] Single cell genotyping of exome sequencing-identified mutations to characterize the clonal composition and evolution of inv(16) AML in a CBL mutated clonal hematopoiesis.2016
Author(s)
Niemoller C, Renz N, Bleul S, Blagitko-Dorfs N, Greil C, Yoshida K, Pfeifer D, Follo M, Duyster J, Claus R, Ogawa S, Lubbert M, Becker H.
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Journal Title
Leuk Res.
Volume: 47
Pages: 41-46
DOI
Peer Reviewed / Open Access / Acknowledgement Compliant
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[Journal Article] Adults with germline CBL mutation complicated with juvenile myelomonocytic leukemia at infancy.2016
Author(s)
Muraoka M, Okuma C, Kanamitsu K, Ishida H, Kanazawa Y, Washio K, Seki M, Kato M, Takita J, Sato Y, Ogawa S, Tsukahara H, Oda M, Shimada A.
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Journal Title
J Hum Genet.
Volume: 61
Pages: 523-526
DOI
Peer Reviewed / Acknowledgement Compliant
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[Journal Article] High-risk HLA alleles for severe acute graft-versus-host disease and mortality in unrelated donor bone marrow transplantation.2016
Author(s)
Morishima S, Kashiwase K, Matsuo K, Azuma F, Yabe T, Sato-Otsubo A, Ogawa S, Shiina T, Satake M, Saji H, Kato S, Kodera Y, Sasazuki T, Morishima Y, Japan Marrow Donor P.
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Journal Title
Haematologica.
Volume: 101
Pages: 491-498
DOI
Peer Reviewed / Open Access / Acknowledgement Compliant
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[Journal Article] Somatic PHF6 mutations in 1760 cases with various myeloid neoplasms.2016
Author(s)
Mori T, Nagata Y, Makishima H, Sanada M, Shiozawa Y, Kon A, Yoshizato T, Sato-Otsubo A, Kataoka K, Shiraishi Y, Chiba K, Tanaka H, Ishiyama K, Miyawaki S, Mori H, Nakamaki T, Kihara R, Kiyoi H, Koeffler HP, Shih LY, Miyano S, Naoe T, Haferlach C, Kern W, Haferlach T, Ogawa S, Yoshida K.
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Journal Title
Leukemia.
Volume: 30
Pages: 2270-2273
DOI
Peer Reviewed / Open Access / Acknowledgement Compliant
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[Journal Article] Somatic mosaicism in chronic myeloid leukemia in remission.2016
Author(s)
Mitani K, Nagata Y, Sasaki K, Yoshida K, Chiba K, Tanaka H, Shiraishi Y, Miyano S, Makishima H, Nakamura Y, Nakamura Y, Ichikawa M, Ogawa S.
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Journal Title
Blood.
Volume: 128
Pages: 2863-2866
DOI
Peer Reviewed / Acknowledgement Compliant
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[Journal Article] Clinical significance and origin of leukocytes that lack HLA-A allele expression in patients with acquired aplastic anemia.2016
Author(s)
Maruyama H, Katagiri T, Kashiwase K, Shiina T, Sato-Otsubo A, Zaimoku Y, Maruyama K, Hosokawa K, Ishiyama K, Yamazaki H, Inoko H, Ogawa S, Nakao S.
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Journal Title
Exp Hematol.
Volume: 44
Pages: 931-939
DOI
Peer Reviewed / Acknowledgement Compliant
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[Journal Article] Functional characterization of a novel GFI1B mutation causing congenital macrothrombocytopenia.2016
Author(s)
Kitamura K, Okuno Y, Yoshida K, Sanada M, Shiraishi Y, Muramatsu H, Kobayashi R, Furukawa K, Miyano S, Kojima S, Ogawa S, Kunishima S.
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Journal Title
J Thromb Haemost.
Volume: 14
Pages: 1462-1469
DOI
Peer Reviewed / Acknowledgement Compliant
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[Journal Article] Clonal dynamics in a single AML case tracked for 9 years reveals the complexity of leukemia progression.2016
Author(s)
Kim T, Yoshida K, Kim YK, Tyndel MS, Park HJ, Choi SH, Ahn JS, Jung SH, Yang DH, Lee JJ, Kim HJ, Kong G, Ogawa S, Zhang Z, Kim HJ, Kim DD.
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Journal Title
Leukemia.
Volume: 30
Pages: 295-302
DOI
Peer Reviewed / Open Access / Acknowledgement Compliant
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[Journal Article] TERT promoter mutations and chromosome 8p loss are characteristic of nonalcoholic fatty liver disease-related hepatocellular carcinoma.2016
Author(s)
Ki Kim S, Ueda Y, Hatano E, Kakiuchi N, Takeda H, Goto T, Shimizu T, Yoshida K, Ikura Y, Shiraishi Y, Chiba K, Tanaka H, Miyano S, Uemoto S, Chiba T, Ogawa S, Marusawa H.
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Journal Title
Int J Cancer.
Volume: 139
Pages: 2512-2518
DOI
Peer Reviewed / Acknowledgement Compliant
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[Journal Article] Genomic analysis of clonal origin of Langerhans cell histiocytosis following acute lymphoblastic leukaemia.2016
Author(s)
Kato M, Seki M, Yoshida K, Sato Y, Oyama R, Arakawa Y, Kishimoto H, Taki T, Akiyama M, Shiraishi Y, Chiba K, Tanaka H, Mitsuiki N, Kajiwara M, Mizutani S, Sanada M, Miyano S, Ogawa S, Koh K, Takita J.
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Journal Title
Br J Haematol.
Volume: 175
Pages: 169-172
DOI
Peer Reviewed / Acknowledgement Compliant
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[Journal Article] Induction of HLA-B*40:02-restricted T cells possessing cytotoxic and suppressive functions against haematopoietic progenitor cells from a patient with severe aplastic anaemia.2016
Author(s)
Inaguma Y, Akatsuka Y, Hosokawa K, Maruyama H, Okamoto A, Katagiri T, Shiraishi K, Murayama Y, Tsuzuki-Iba S, Mizutani Y, Nishii C, Yamamoto N, Demachi-Okamura A, Kuzushima K, Ogawa S, Emi N, Nakao S.
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Journal Title
Br J Haematol.
Volume: 172
Pages: 131-134
DOI
Peer Reviewed / Acknowledgement Compliant
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[Journal Article] PIEZO1 gene mutation in a Japanese family with hereditary high phosphatidylcholine hemolytic anemia and hemochromatosis-induced diabetes mellitus.2016
Author(s)
Imashuku S, Muramatsu H, Sugihara T, Okuno Y, Wang X, Yoshida K, Kato A, Kato K, Tatsumi Y, Hattori A, Kita S, Oe K, Sueyoshi A, Usui T, Shiraishi Y, Chiba K, Tanaka H, Miyano S, Ogawa S, Kojima S, Kanno H.
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Journal Title
Int J Hematol.
Volume: 104
Pages: 125-129
DOI
Peer Reviewed / Acknowledgement Compliant
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[Journal Article] ALDH2 polymorphism in patients with Diamond-Blackfan anemia in Japan.2016
Author(s)
Ikeda F, Toki T, Kanezaki R, Terui K, Yoshida K, Kanno H, Ohga S, Ohara A, Kojima S, Ogawa S, Ito E.
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Journal Title
Int J Hematol.
Volume: 103
Pages: 112-114
DOI
Peer Reviewed / Acknowledgement Compliant
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[Journal Article] ATP11C is a major flippase in human erythrocytes and its defect causes congenital hemolytic anemia.2016
Author(s)
Arashiki N, Takakuwa Y, Mohandas N, Hale J, Yoshida K, Ogura H, Utsugisawa T, Ohga S, Miyano S, Ogawa S, Kojima S, Kanno H.
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Journal Title
Haematologica.
Volume: 101
Pages: 559-565
DOI
Peer Reviewed / Acknowledgement Compliant
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[Presentation] 淡明細胞型腎細胞癌における血漿循環腫瘍DNA解析の有用性の検討2016
Author(s)
Yusuke Sato, Yoichi Fujii, Kenichi Yoshida, Yuichi Shiraishi, Kenichi Chiba, Hiroko Tanaka, Hideki Makishima, Tohru Nakagawa, Haruki Kume, Satoru Miyano, Seishi Ogawa, Yukio Homma
Organizer
第54回日本癌治療学会学術集会
Place of Presentation
横浜
Year and Date
2016-11-13 – 2016-11-13
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[Presentation] Molecular profiling across different subtypes of B-cell lymphoma2016
Author(s)
Yasunori Kogure, Keisuke Kataoka, Kenichi Yoshida, Yuichi Shiraishi, Kenichi Chiba, Hiroko Tanaka, Tetsuichi Yoshizato, Yasunobu Nagata, Masashi Sanada, Motohiro Kato, Hiraku Mori, Yasuharu Sato, Tadashi Yoshino, Kengo Takeuchi, Yuichi Ishikawa, Satoru Miyano, Seishi Ogawa
Organizer
The 78th Annual Meeting of the Japanese Society of Hematology
Place of Presentation
横浜
Year and Date
2016-10-15 – 2016-10-15
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[Presentation] The biological characterization of Srsf2 P95H mutation in the pathogenesis of myelodysplasia2016
Author(s)
Ayana Kon, Satoshi Yamazaki, Yusuke Shiozawa, Keisuke Kataoka, Yasunori Ota, Maiko Morita, Tetsuichi Yoshizato, Masashi Sanada, Kenichi Yoshida, Hideki Makisima, Yasuhito Nanya, Shinichi Kotani, June Takeda, Yosaku Watatani, Yotaro Ochi, Manabu Nakayama, Haruhiko Koseki, Hiromitsu Nakauchi, Seishi Ogawa
Organizer
The 78th Annual Meeting of the Japanese Society of Hematology
Place of Presentation
横浜
Year and Date
2016-10-13 – 2016-10-13
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[Presentation] Clonal evolution following azacitidine therapy in patients with high-risk myelodysplastic syndromes2016
Author(s)
June Takeda, Kenichi Yoshida, Tetsuichi Yoshizato, Yusuke Shiozawa, Hideki Makishima, Yasuhito Nannya, Hiromichi Suzuki, Yuichi Shiraishi, Yusuke Okuno, Kenichi Chiba, Satoru Miyano, Masashi Sanada, Toru Kiguchi, Nobuaki Dobashi , Kensuke Usuki, Shigeru Chiba, Norio Asou, Yasuyuki Miyazaki, Tomoki Naoe, Hitoshi Kiyoi
Organizer
The 78th Annual Meeting of the Japanese Society of Hematology
Place of Presentation
横浜
Year and Date
2016-10-13 – 2016-10-13
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[Presentation] Landscape of MDS genomes as revealed by whole genome sequencing.2016
Author(s)
Yasuhito Nannya, Kenichi Yoshida, Keisuke Kataoka, Yasunobu Nagata, Tetsuichi Yoshizato, Toru Kiguchi, Nobuaki Dobashi, Kensuke Usuki, Tomoki Naoe, Yukio Kobayashi, Hitoshi Kiyoi, Shigeru Chiba, Norio Aso, Yasushi Miyazaki, Hiroko Tanaka, Kenichi Chiba, Yuichi Shiraishi, Satoru Miyano, and Seishi Ogawa
Organizer
The 78th Annual Meeting of the Japanese Society of Hematology
Place of Presentation
横浜
Year and Date
2016-10-13 – 2016-10-13
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[Presentation] 淡明細胞型腎細胞癌における血漿循環腫瘍DNA解析の有用性の検討2016
Author(s)
Yusuke Sato, Yoichi Fujii, Kenichi Yoshida, Yuichi Shiraishi, Kenichi Chiba, Hiroko Tanaka, Hideki Makishima, Tohru Nakagawa, Haruki Kume, Satoru Miyano, Seishi Ogawa, Yukio Homma
Organizer
The 75th Annual Meeting of the Japanese Cancer Association
Place of Presentation
横浜
Year and Date
2016-10-07 – 2016-10-07
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[Presentation] The carcinogenic sequence in colitis-associated cancer2016
Author(s)
Nobuyuki Kakiuchi, Kenichi Yoshida, Yusuke Shiozawa, Kenichi Chiba, Yuichi Shiraishi, Takaki Sakurai, Yoshiharu Sakai, Motoi Uchino, Seiichi Hirota, Hiroki Ikeuchi, Satoru Miyano, Hiroyuki Marusawa, Seishi Ogawa
Organizer
The 75th Annual Meeting of the Japanese Cancer Association
Place of Presentation
横浜
Year and Date
2016-10-07 – 2016-10-07
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[Presentation] Genetic landscape of primary central nervous system lymphoma2016
Author(s)
Kenichi Yoshida, Kenichi Chiba, Yusuke Okuno, Hiromichi Suzuki, Yuichi Shiraishi, Hiroko Tanaka, Yoshihiro Muragaki, Takashi Shiina, Satoru Miyano, Shigeru Chiba, Ryuya Yamanaka, Seishi Ogawa
Organizer
The 75th Annual Meeting of the Japanese Cancer Association
Place of Presentation
横浜
Year and Date
2016-10-07 – 2016-10-07
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[Presentation] Clonal structure and oncogenic potential of liver cirrhosis tissues2016
Author(s)
Soo Ki Kim, Kenichi Yoshida, Yoshihide Ueda, Sachiko Minamiguchi, Toshimi Kaido, Yuichi Shiraishi, Satoru Miyano, Hironori Haga, Shinji Uemoto, Hiroshi Seno, Seishi Ogawa, Hiroyuki Marusawa
Organizer
The 75th Annual Meeting of the Japanese Cancer Association
Place of Presentation
横浜
Year and Date
2016-10-07 – 2016-10-07
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[Presentation] Molecular profiling across different subtypes of B-cell lymphoma2016
Author(s)
Yasunori Kogure, Keisuke Kataoka, Kenichi Yoshida, Yuichi Shiraishi, Kenichi Chiba, Hiroko Tanaka, Masashi Sanada, Motohiro Kato, Tadashi Yoshino, Kengo Takeuchi, Yuichi Ishikawa, Satoru Miyano, Seishi Ogawa
Organizer
The 75th Annual Meeting of the Japanese Cancer Association
Place of Presentation
横浜
Year and Date
2016-10-07 – 2016-10-07
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[Presentation] The 75th Annual Meeting of the Japanese Cancer Association2016
Author(s)
Akira Yokoyama, Hiromichi Suzuki, Tetsuichi Yoshizato, Yusuke Shiozawa, Yusuke Sato, Kosuke Aoki, Nobuyuki Kakiuchi, Yasuhide Takeuchi, Shigeru Tsunoda, Masashi Sanada, Satoru Miyano, Manabu Muto, Seishi Ogawa
Organizer
Differential role of mutations in clonal evolution in esophaegal mucosal in high-risk individuals for cancer
Place of Presentation
横浜
Year and Date
2016-10-06 – 2016-10-06
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[Presentation] Impact of somatic mutations on outcome in patients with MDS after stem-cell transplantation2016
Author(s)
Tetsuichi Yoshizato, Yusuke Shiozawa, Kenichi Yoshida, Yoshiko Atsuta, Nannya Yasuhito, Hiromichi Suzuki, Makoto Onizuka, Keisuke Kataoka, Kenichi Chiba, Hiroko Tanaka, Yuichi Shiraishi, Kousuke Aoki, Masashi Sanada, Hidehiro Itonaga, Yoshinobu Kanda, Yasushi Miyazaki, Hideki Makishima, Satoru Miyano, and Seishi Ogawa
Organizer
The 75th Annual Meeting of the Japanese Cancer Association
Place of Presentation
横浜
Year and Date
2016-10-06 – 2016-10-06
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[Presentation] Landscape of MDS genomes as revealed by whole genome sequencing.2016
Author(s)
Yasuhito Nannya, Kenichi Yoshida, Keisuke Kataoka, Yasunobu Nagata, Tetsuichi Yoshizato, Shigeru Chiba, Norio Aso, Yasushi Miyazaki, Hiroko Tanaka, Kenichi Chiba, Yuichi Shiraishi, Satoru Miyano, and Seishi Ogawa
Organizer
The 75th Annual Meeting of the Japanese Cancer Association
Place of Presentation
横浜
Year and Date
2016-10-06 – 2016-10-06
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[Presentation] Prognostic Relevance of Integrated Molecular Profiling in Adult T-cell Leukemia/Lymphoma2016
Author(s)
Yotaro Ochi, Keisuke Kataoka, Yasunobu Nagata, Akira Kitanaka, Jun-ichiro Yasunaga, Masako Iwanaga, Kisato Nosaka, Hidehiro Itonaga, Yositaka Imaizumi, Kotaro Shide, Yasushi Miyazaki, Akifumi Takaori-Kondo, Kazuya Shimoda, Masao Matsuoka, Toshiki Watanabe, Seishi Ogawa
Organizer
第3回日本HTLV-1学会学術集会
Place of Presentation
Kagoshima, Japan
Year and Date
2016-08-27 – 2016-08-27
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[Presentation] ATLおよびT細胞リンパ腫における遺伝子変異プロファイルの解析2016
Author(s)
Yosaku Watatani, Yasuharu Sato, Kenji Nishida, Hiroaki Miyoshi, Yuichi Shiraishi, Kenichi Chiba, Hiroko Tanaka, Hiroo Ueno, Nobuyuki Kakiuchi, Yusuke Shiozawa, Tetsuichi Yoshizato, Kenichi Yoshida, Masashi Sanada, Satoru Miyano, Koichi Ohshima, Tadashi Yoshino, Seishi Ogawa, Keisuke Kataoka
Organizer
第3回日本HTLV-1学会学術集会
Place of Presentation
Kagoshima, Japan
Year and Date
2016-08-27 – 2016-08-27
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[Presentation] Impact of somatic mutations on outcome in patients with MDS after stem-cell transplantation2016
Author(s)
Tetsuichi Yoshizato, Yusuke Shiozawa, Kenichi Yoshida, Yoshiko Atsuta, Nannya Yasuhito, Hiromichi Suzuki, Makoto Onizuka, Keisuke Kataoka, Kenichi Chiba, Hiroko Tanaka, Yuichi Shiraishi, Kousuke Aoki, Masashi Sanada, Hidehiro Itonaga, Yoshinobu Kanda, Yasushi Miyazaki, Hideki Makishima, Satoru Miyano, and Seishi Ogawa
Organizer
The 21st Congress of European Hematology Association
Place of Presentation
Copenhagen, Denmark
Year and Date
2016-06-10 – 2016-06-10
Int'l Joint Research
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[Presentation] GENETIC PREDISPOSITIONS TO SPORADIC MYELOID NEOPLASMS CAUSED BY GERMLINE DDX41 MUTATIONS IN ASIAN AND CAUCASIAN POPULATIONS.2016
Author(s)
June Takeda, Kenichi Yoshida, Hideki Makishima, Tetsuichi Yoshizato, Yusuke Shiozawa, Hiromichi Suzuki, Yuichi Shiraishi, Yusuke Okuno, Ayana Kon, Keisuke Kataoka, Kenichi Chiba, Hiroko Tanaka, Masashi Sanada, Chantana Polprasert, Jaroslaw P. Maciejewski, and Seishi Ogawa
Organizer
The 21st Congress of European Hematology Association (国際学会)
Place of Presentation
Copenhagen, Denmark
Year and Date
2016-06-10 – 2016-06-10
Int'l Joint Research
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[Presentation] Clinical and biological landscape of driver mutations in pediatric acute lymphoblastic leukemia2016
Author(s)
Hiroo Ueno, Yuka Yamashita Kenichi Yoshida, Yusuke Shiozawa, Satomi Ishida, Hiroyuki Tsukamoto, Mayumi Kibe, Yuichi Shiraishi, Hiroko Tanaka, Kenichi Chiba, Takao Deguchi, Atsushi Sato, Yoshiko Hashii, Toshihiko Imamura, Satoru Miyano, Seishi Ogawa, Keizo Horibe, Masashi Sanada
Organizer
The 21st European Hematology Association congress
Place of Presentation
Copenhagen, Denmark
Year and Date
2016-06-09 – 2016-06-09
Int'l Joint Research
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[Presentation] MDS Genomics and its Clincial Implication.2016
Author(s)
Hideki Makishima, Tetsuichi Yoshizato, Kenichi Yoshida, Yasunobu Nagata, Mikkael Sekeres, Yusuke Okuno, Yuichi Shiraishi, Shigeru Chiba, Satoru Miyano, Lee-Yung Shih, Torsten Haferlach, Seishi Ogawa, Jaroslaw Maciejewski.
Organizer
The 5th National Conference on Hematologic Oncology
Place of Presentation
Nanjing,China
Year and Date
2016-05-21 – 2016-05-21
Int'l Joint Research / Invited
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[Presentation] 淡明細胞型腎細胞癌における血漿循環腫瘍DNA解析の有用性の検討2016
Author(s)
Yusuke Sato, Yoichi Fujii, Tohru Nakagawa, Haruki Kume, Yuichi Shiraishi, Satoru Miyano, Seishi Ogawa, Yukio Homma
Organizer
The 104th Annual Meeting of the Japanese Urological Association
Place of Presentation
Sendai, Japan
Year and Date
2016-04-23 – 2016-04-23
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[Presentation] Impact of Somatic Mutations on Outcome in Patients with MDS after Stem-Cell Transplantation2016
Author(s)
Tetsuichi Yoshizato, Yusuke Shiozawa, Kenichi Yoshida, Yoshiko Atsuta, Nannya Yasuhito, Hiromichi Suzuki, Makoto Onizuka, Keisuke Kataoka, Kenichi Chiba, Hiroko Tanaka, Yuichi Shiraishi, Kousuke Aoki, Masashi Sanada, Hidehiro Itonaga, Yoshinobu Kanda, Yasushi Miyazaki, Hideki Makishima, Satoru Miyano, and Seishi Ogawa
Organizer
International Conference on Myelodysplastic Syndromes
Place of Presentation
Estoril,Portugal
Year and Date
2016-04-14 – 2016-04-14
Int'l Joint Research
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[Presentation] Cancer Genetics 4.2016
Author(s)
Hideki Makishima, Tetsuichi Yoshizato, Kenichi Yoshida, Yasunobu Nagata, Mikkael Sekeres, Yusuke Okuno, Yuichi Shiraishi, Shigeru Chiba, Satoru Miyano, Lee-Yung Shih, Torsten Haferlach, Seishi Ogawa, Jaroslaw Maciejewski.
Organizer
The 13th International Congress of Human Genetics (ICHG2016)
Place of Presentation
京都
Year and Date
2016-04-07 – 2016-04-07
Int'l Joint Research / Invited