نتایج جستجو برای: ژن npm1

تعداد نتایج: 16927  

Journal: :Blood 2012
Jochen Greiner Yoko Ono Susanne Hofmann Anita Schmitt Elmar Mehring Marlies Götz Philippe Guillaume Konstanze Döhner Joannis Mytilineos Hartmut Döhner Michael Schmitt

Mutations in the nucleophosmin gene (NPM1(mut)) are one of the most frequent molecular alterations in acute myeloid leukemia (AML), and immune responses may contribute to the favorable prognosis of AML patients with NPM1(mut). In the present study, we were able to demonstrate both CD4(+) and CD8(+) T-cell responses against NPM1(mut). Ten peptides derived from wild-type NPM1 and NPM1(mut) were s...

Journal: :Blood 2005
Tatsuya Suzuki Hitoshi Kiyoi Kazutaka Ozeki Akihiro Tomita Satomi Yamaji Ritsuro Suzuki Yoshihisa Kodera Shuichi Miyawaki Norio Asou Kazutaka Kuriyama Fumiharu Yagasaki Chihiro Shimazaki Hideki Akiyama Miki Nishimura Toshiko Motoji Katsuji Shinagawa Akihiro Takeshita Ryuzo Ueda Tomohiro Kinoshita Nobuhiko Emi Tomoki Naoe

Recently, somatic mutations of the nucleophosmin gene (NPM1), which alter the subcellular localization of the product, have been reported in acute myeloid leukemia (AML). We analyzed the clinical significance of NPM1 mutations in comparison with cytogenetics, FLT3, NRAS, and TP53 mutations, and a partial tandem duplication of the MLL gene (MLL-TD) in 257 patients with AML. We found NPM1 mutatio...

2012
Shiu-Huey Chou Bor-Sheng Ko Ji-Shain Chiou Yueh-Chwen Hsu Mong-Hsun Tsai Yu-Chiao Chiu I-Shing Yu Shu-Wha Lin Hsin-An Hou Yi-Yi Kuo Hsiu-Mei Lin Ming-Fang Wu Wen-Chien Chou Hwei-Fang Tien

Somatic Nucleophosmin (NPM1) mutation frequently occurs in acute myeloid leukemia (AML), but its role in leukemogenesis remains unclear. This study reports the first "conventional" knock-in mouse model of Npm1 mutation, which was achieved by inserting TCTG after nucleotide c.857 (c.854_857dupTCTG) to mimic human mutation without any "humanized" sequence. The resultant mutant peptide differed sl...

Journal: :Blood 2005
Konstanze Döhner Richard F Schlenk Marianne Habdank Claudia Scholl Frank G Rücker Andrea Corbacioglu Lars Bullinger Stefan Fröhling Hartmut Döhner

To assess the prognostic relevance of mutations in the NPM1 gene encoding a nucleocytoplasmic shuttle protein in younger adults with acute myeloid leukemia (AML) and normal cytogenetics, sequencing of NPM1 exon 12 was performed in diagnostic samples from 300 patients entered into 2 consecutive multicenter trials of the AML Study Group (AMLSG). Treatment included intensive double-induction thera...

Journal: :The EMBO journal 2011
Fumihiko Sagawa Hend Ibrahim Angela L Morrison Carol J Wilusz Jeffrey Wilusz

During polyadenylation, the multi-functional protein nucleophosmin (NPM1) is deposited onto all cellular mRNAs analysed to date. Premature termination of poly(A) tail synthesis in the presence of cordycepin abrogates deposition of the protein onto the mRNA, indicating natural termination of poly(A) addition is required for NPM1 binding. NPM1 appears to be a bona fide member of the complex invol...

Journal: :Blood 2011
Matthias Schwab Elke Schaeffeler

ence is sufficient to disrupt the nucleolar structure.9 Similarly, the anticancer peptide CIGB-300 leads to nucleolar disassembly and apoptosis, most likely through its capability to bind NPM1.10 Because AML cells carrying the NPM1 mutation are depleted of wild-type NPM1 protein in their nucleolar pool (because of haploinsufficiency and cytoplasmic dislocation through formation of heterodimers ...

2012
Cheng-Der Liu Ya-Lin Chen Yi-Li Min Bo Zhao Chi-Ping Cheng Myung-Soo Kang Shu-Jun Chiu Elliott Kieff Chih-Wen Peng

Epstein-Barr Virus (EBV) is an oncogenic γ-herpesvirus that capably establishes both latent and lytic modes of infection in host cells and causes malignant diseases in humans. Nuclear antigen 2 (EBNA2)-mediated transcription of both cellular and viral genes is essential for the establishment and maintenance of the EBV latency program in B lymphocytes. Here, we employed a protein affinity pull-d...

Journal: :Leukemia research 2008
Meilani Syampurnawati Eiji Tatsumi Bambang Ardianto Mariko Takenokuchi Yuji Nakamachi Seiji Kawano Shun-ichi Kumagai Katsuyasu Saigo Toshimitsu Matsui Takayuki Takahashi Ken-ichi Nagai Gunadi Hisahide Nishio Hiroki Yabe Shin-Ichi Kondo Yoshitake Hayashi

Our previous observation of a higher incidence of FLT3-ITD in DR(-) M1/M2 AML than in DR(+) M1/M2 led to an investigation of NPM1 mutation in the same samples, since DR(-) AML and AML with NPM1 mutation share such characteristics as normal karyotype, the absence of CD34, and FLT3-ITD. NPM1 mutation was found in 18 of 26 (69.2%) of DR(-) cases, but not in any of 28 DR(+) cases. FLT3-ITD was note...

2013
Pradeep Singh Chauhan Rakhshan Ihsan L. C. Singh Dipendra Kumar Gupta Vishakha Mittal Sujala Kapur

BACKGROUND Mutations in NPM1 and FLT3 genes represent the most frequent genetic alterations and important diagnostic and prognostic indicators in patients with acute myeloid leukemia (AML). OBJECTIVE We investigated the prevalence and clinical characteristics of NPM1 and FLT3 mutations in 161 patients of de novo AML including adults and children. RESULTS NPM1 mutation was found in 21% and F...

Journal: :Blood 2011
Ramesh Balusu Warren Fiskus Rekha Rao Daniel G Chong Srilatha Nalluri Uma Mudunuru Hongwei Ma Lei Chen Sreedhar Venkannagari Kyungsoo Ha Sunil Abhyankar Casey Williams Joseph McGuirk Hanna Jean Khoury Celalettin Ustun Kapil N Bhalla

Nucleophosmin 1 (NPM1) is an oligomeric, nucleolar phosphoprotein that functions as a molecular chaperone for both proteins and nucleic acids. NPM1 is mutated in approximately one-third of patients with AML. The mutant NPM1c+ contains a 4-base insert that results in extra C-terminal residues encoding a nuclear export signal, which causes NPM1c+ to be localized in the cytoplasm. Here, we determi...

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