4.1 Article

Ring/marker chromosome derived from chromosome 7 in childhood acute megakaryoblastic leukemia with monosomy 7

Journal

INTERNATIONAL JOURNAL OF HEMATOLOGY
Volume 92, Issue 2, Pages 386-390

Publisher

SPRINGER JAPAN KK
DOI: 10.1007/s12185-010-0663-0

Keywords

Monosomy 7; Spectral karyotyping; Fluorescence in situ hybridization

Categories

Ask authors/readers for more resources

In some cases of childhood acute megakaryoblastic leukemia (AMKL), G-band analysis reveals supernumerary ring/marker chromosomes along with monosomy 7. However, their origin and relevance are poorly understood. We experienced three patients with AMKL, one of whom had Down's syndrome, whose blasts at the first visit exhibited both monosomy 7 and a ring/marker chromosome. For one case, precise molecular-cytogenetic techniques revealed that the ring chromosome was derived from a chromosome 7. It was strongly suggested that the ring chromosome was derived from a chromosome 7 in another case. The ring or one of the 2 marker chromosomes was derived from a chromosome 7 in the other case. All patients responded well to initial induction therapy. While it is not clear whether the ring/marker chromosome 7 affects the long-term prognosis of acute myeloid leukemia with monosomy 7, it may be of prognostic relevance to distinguish pure monosomy 7 from monosomy 7 with a ring/marker chromosome 7. For this purpose, conventional G-banding could be complemented with additional techniques such as spectral karyotyping or fluorescence in situ hybridization, which characterize the aberration in more detail. These methods may be useful for determining the optimal treatment and for elucidating the etiology of AMKL itself.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.1
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

Article Oncology

Randomized Phase II Study of Consecutive-Day versus Alternate-Day Treatment with S-1 as Second-Line Chemotherapy in Advanced Pancreatic Cancer

Takuya Ishikawa, Hiroki Kawashima, Eizaburo Ohno, Hiroshi Matsubara, Yoji Sasaki, Koichi Achiwa, Akira Kanamori, Hajime Sumi, Takanori Hirai, Koji Nonogaki, Tomoyuki Tsuzuki, Masanori Kuroiwa, Masashi Hattori, Shinya Maruta, Takeshi Hiramatsu, Masahiko Ando, Senju Hashimoto, Yoshiki Hirooka

ONCOLOGY (2019)

Article Gastroenterology & Hepatology

Comparison of 8-and 10-mm diameter fully covered self-expandable metal stents: A multicenter prospective study in patients with distal malignant biliary obstruction

Hiroki Kawashima, Senju Hashimoto, Eizaburo Ohno, Takuya Ishikawa, Tomomasa Morishima, Hiroshi Matsubara, Hiroyuki Sugimoto, Koji Nonogaki, Akira Kanamori, Kazuo Hara, Takamichi Kuwahara, Masanao Nakamura, Ryoji Miyahara, Masatoshi Ishigami, Masahiko Ando, Yoshiki Hirooka

DIGESTIVE ENDOSCOPY (2019)

Article Chemistry, Organic

Atom-economical brominations with tribromide complexes in the presence of oxidants

Kotaro Yubata, Hiroshi Matsubara

TETRAHEDRON LETTERS (2019)

Review Chemistry, Organic

Second Generation Phase-vanishing Method

Hiroshi Matsubara

JOURNAL OF SYNTHETIC ORGANIC CHEMISTRY JAPAN (2019)

Article Chemistry, Organic

Hydrodecyanation of Secondary Alkyl Nitriles and Malononitriles to Alkanes using DiMelmd-BH3

Takuji Kawamoto, Kyohei Oritani, Atsushi Kawabata, Tsubasa Morioka, Hiroshi Matsubara, Akio Kamimura

JOURNAL OF ORGANIC CHEMISTRY (2020)

Article Gastroenterology & Hepatology

Usefulness of endoscopic ultrasound-guided fine-needle biopsy for the diagnosis of autoimmune pancreatitis using a 22-gauge Franseen needle: a prospective multicenter study

Takuya Ishikawa, Hiroki Kawashima, Eizaburo Ohno, Hiroki Suhara, Daijuro Hayashi, Takeshi Hiramatsu, Hiroshi Matsubara, Takahisa Suzuki, Takamichi Kuwahara, Eri Ishikawa, Yoshie Shimoyama, Fumie Kinoshita, Yoshiki Hirooka, Mitsuhiro Fujishiro

ENDOSCOPY (2020)

Article Biochemistry & Molecular Biology

New approach to prepare fluorogenic branched dextrins for assaying glycogen debranching enzyme

Miyu Sakaguchi, Yasushi Makino, Hiroshi Matsubara

GLYCOCONJUGATE JOURNAL (2020)

Article Chemistry, Organic

Borane evolution and its application to organic synthesis using the phase-vanishing method

Nene Soga, Tomo Yoshiki, Aoi Sato, Takuji Kawamoto, Ilhyong Ryu, Hiroshi Matsubara

Summary: In this study, borane was generated in situ using a PV method from NaBH4 or (Bu4NBH4)-Bu-n and reacted with alkenes to produce alcohols. The evolved borane was also used for selective reduction of carboxylic acids and successful Suzuki-Miyaura coupling. The PV system allowed easy and safe reactions with borane in common test tubes.

TETRAHEDRON LETTERS (2021)

Article Chemistry, Multidisciplinary

Redox-Neutral Tetrafluoroethylation of Aryl Alkynes with 1,1,2,2-Tetrafluoroethane Sulfonic Acid Leading to α-Tetrafluoroethylated Acetophenones

Takuji Kawamoto, Kohki Noguchi, Ryotaro Takata, Rio Sasaki, Hiroshi Matsubara, Akio Kamimura

Summary: The redox-neutral tetrafluoroethylation of alkynes with TFESA and AIBN proceeds through the formation of vinyl tetrafluoroethanesulfonates followed by a radical tetrafluoroethylation. Both experimental and theoretical results support an intermolecular reaction mechanism.

CHEMISTRY-A EUROPEAN JOURNAL (2021)

Article Biochemistry & Molecular Biology

Glycogen debranching pathway deduced from substrate specificity of glycogen debranching enzyme

Ayato Ikeda, Yasushi Makino, Hiroshi Matsubara

Summary: Glycogen debranching enzyme (GDE) has both 4-alpha-glucanotransferase and amylo-alpha-1,6-glucosidase activities. This study analyzed the substrate specificities of these enzymes and proposed a macroscopic debranching pathway.

GLYCOCONJUGATE JOURNAL (2022)

Article Chemistry, Organic

Preparation and properties of novel hetero-halogen complexes

Yuji Nishidai, Toshiki Kawabata, Kotaro Yubata, Fumiya Ota, Hiroki Takamiya, Hideki Fujiwara, Hiroshi Matsubara

Summary: In this study, a new method for the preparation of hetero-halogen compounds was developed. Two novel air-stable hetero-halogen complexes were synthesized and utilized for the one-step synthesis of various hetero-halogen compounds.

TETRAHEDRON (2022)

Article Chemistry, Applied

Gold-Catalyzed Oxyarylation/Hydroxylation of N-Alkoxypropiolamides for Chemoselective Synthesis of 4-Aryl-3-(2H)-isoxazolones

Motohiro Yasui, Naoko Tahara, Hiroshi Matsubara, Norihiko Takeda, Masafumi Ueda

Summary: This study developed a sequential gold-catalyzed reaction for synthesizing 4-aryl-3-(2H)-isoxazolones with a hydroxy group. The method allows the introduction of an aryl and hydroxy group in a single procedure, exhibiting good chemoselectivity and tolerance towards reactive functional groups.

ADVANCED SYNTHESIS & CATALYSIS (2022)

Article Chemistry, Organic

Safe and facile evolution of diazomethane using the phase-vanishing method

Toshiki Kawabata, Hiroshi Matsubara

Summary: Although diazomethane is highly explosive, the phase-vanishing method using highly fluorinated solvents was employed to safely generate it for organic synthesis. A two-chamber reactor was used to gradually evolve and consume diazomethane under PV conditions, such as the methylation of carboxylic acids. This PV system provides a facile and safe method for the generation of hazardous diazomethane.

TETRAHEDRON LETTERS (2023)

Article Chemistry, Physical

Structural elucidation of C5H7+ derived from 3-methyl-1,4-pentadiene using ion-mobility spectrometry

Kenichi Iwamoto, Genki Inoue, Hiroshi Matsubara

Summary: The C5H7+ fragment ion derived from 3-methyl1,4-pentadiene (MPD) was investigated using an ion mobility/mass spectrometer. The reduced mobilities (K0) of the C5H7+ fragment ions generated by MPD and cyclohexene correlated with effective temperature in He buffer gas, indicating that these fragments were identical cyclopentenium cations. Density functional theory calculations revealed the feasibility of the dissociation of MPD to cyclopentenium cations.

CHEMICAL PHYSICS LETTERS (2023)

Article Chemistry, Organic

A computational study of site-selective hydrogen abstraction by sulfate radical anion

Masahiro Ueda, Atsuki Kitano, Hiroshi Matsubara

Summary: The selective hydrogen abstraction reactions on sp(3) carbons with oxyradicals were investigated using ab initio and DFT calculations. It was found that beta-hydrogen abstraction was favorable, consistent with experimental findings. NBO analysis revealed that the transferred hydrogen atom is partially positively charged when abstracted by an oxyradical, and hydrogens bonded to the most positively charged carbon in the substrate were predominantly abstracted, providing a simple compass for predicting regioselectivity in the functionalization of C(sp(3))-H bonds with oxyradicals.

ORGANIC & BIOMOLECULAR CHEMISTRY (2021)

No Data Available