نتایج جستجو برای: bcl2 gene

تعداد نتایج: 1143652  

Journal: :Cell 2002
Gaël G. McGill Martin Horstmann Hans R. Widlund Jinyan Du Gabriela Motyckova Emi K. Nishimura Yi-Ling Lin Sridhar Ramaswamy William Avery Han-Fei Ding Siobhán A. Jordan Ian J. Jackson Stanley J. Korsmeyer Todd R. Golub David E. Fisher

Kit/SCF signaling and Mitf-dependent transcription are both essential for melanocyte development and pigmentation. To identify Mitf-dependent Kit transcriptional targets in primary melanocytes, microarray studies were undertaken. Among identified targets was BCL2, whose germline deletion produces melanocyte loss and which exhibited phenotypic synergy with Mitf in mice. BCL2's regulation by Mitf...

2015
Guo Chen Xingming Deng

The decision phase of apoptosis is mainly regulated by the Bcl-2 family, which renders these proteins potential targets for cancer therapy through apoptotic mechanisms. Bcl2 family members have homology clustered within four conserved Bcl2 homology (BH) domains (BH1, BH2, BH3 and BH4). Only the antiapoptotic proteins, such as Bcl2, Bcl-XL, Bcl-w and A1, bear the NH 2-terminal BH4 domain [1]. Mc...

Journal: :Acta medica Indonesiana 2006
Amaylia Oehadian Naoki Koide Pandji Irani Fianza Trinugroho Heri Fadjari Rachmat Sumantri Iman Supandiman Takashi Yokochi

AIM Gene rearrangement has an important role in the management of lymphoma. We investigated the rearrangements of B-cell leukaemia/lymphoma 2 (BCL2), BCL6 and Paired homeobox 5 (PAX5) genes in Indonesian follicular lymphoma (FL) patients. METHODS We examined gene rearrangements using various kinds of polymerase chain reactions (PCRs) on 24 patients' peripheral blood DNA. RESULTS BCL2 rearra...

2015
Alexandar Tzankov Nora Leu Simone Muenst Darius Juskevicius Dirk Klingbiel Christoph Mamot Stephan Dirnhofer

BACKGROUND The prognostic role of tumor-related parameters in diffuse large B cell lymphoma (DLBCL) is a matter of controversy. METHODS We investigated the prognostic value of phenotypic and genotypic profiles in DLBCL in clinical trial (NCT00544219) patients homogenously treated with six cycles of rituximab, cyclophosphamide, hydroxydaunorubicin, vincristine, prednisone (R-CHOP), followed by...

Journal: :Cancer research 2012
Chaitali Dutta Tovah Day Nadja Kopp Diederik van Bodegom Matthew S Davids Jeremy Ryan Liat Bird Naveen Kommajosyula Oliver Weigert Akinori Yoda Hua Fung Jennifer R Brown Geoffrey I Shapiro Anthony Letai David M Weinstock

BCL2 suppresses apoptosis by binding the BH3 domain of proapoptotic factors and thereby regulating outer mitochondrial membrane permeabilization. Many tumor types, including B-cell lymphomas and chronic lymphocytic leukemia, are dependent on BCL2 for survival but become resistant to apoptosis after treatment. Here, we identified a direct interaction between the antiapoptotic protein BCL2 and th...

2016
Masoumeh Falah Mohammad Najafi Massoud Houshmand Mohammad Farhadi

Age-related hearing impairment (ARHI) is a progressive and a common sensory disorder in the elderly and will become an increasingly important clinical problem given the growing elderly population. Apoptosis of cochlear cells is an important factor in animal models of ARHI. As these cells cannot regenerate, their loss leads to irreversible hearing impairment. Identification of molecular mechanis...

Journal: :Molecular oncology 2014
Anieta M Sieuwerts Maria B Lyng Marion E Meijer-van Gelder Vanja de Weerd Fred C G J Sweep John A Foekens Paul N Span John W M Martens Henrik J Ditzel

To identify molecular markers indicative of response to tamoxifen and easily implemented in the routine setting, we recently reported three gene signatures that could stratify post-menopausal tamoxifen-treated, estrogen receptor-positive (ER+) patients according to outcome in the adjuvant setting. Here, we evaluated the predictive potential of the total of 14 genes included in the 3 gene signat...

Journal: :Blood 2017
Alyssa Bouska Chengfeng Bi Waseem Lone Weiwei Zhang Ambreen Kedwaii Tayla Heavican Cynthia M Lachel Jiayu Yu Roberto Ferro Nanees Eldorghamy Timothy C Greiner Julie Vose Dennis D Weisenburger Randy D Gascoyne Andreas Rosenwald German Ott Elias Campo Lisa M Rimsza Elaine S Jaffe Rita M Braziel Reiner Siebert Rodney R Miles Sandeep Dave Anupama Reddy Jan Delabie Louis M Staudt Joo Y Song Timothy W McKeithan Kai Fu Michael Green Wing C Chan Javeed Iqbal

The adult high-grade B-cell lymphomas sharing molecular features with Burkitt lymphoma (BL) are highly aggressive lymphomas with poor clinical outcome. High-resolution structural and functional genomic analysis of adult Burkitt lymphoma (BL) and high-grade B-cell lymphoma with BL gene signature (adult-molecularly defined BL [mBL]) revealed the MYC-ARF-p53 axis as the primary deregulated pathway...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 2005
Amelia Cimmino George Adrian Calin Muller Fabbri Marilena V Iorio Manuela Ferracin Masayoshi Shimizu Sylwia E Wojcik Rami I Aqeilan Simona Zupo Mariella Dono Laura Rassenti Hansjuerg Alder Stefano Volinia Chang-Gong Liu Thomas J Kipps Massimo Negrini Carlo M Croce

Chronic lymphocytic leukemia (CLL) is the most common human leukemia and is characterized by predominantly nondividing malignant B cells overexpressing the antiapoptotic B cell lymphoma 2 (Bcl2) protein. miR-15a and miR-16-1 are deleted or down-regulated in the majority of CLLs. Here, we demonstrate that miR-15a and miR-16-1 expression is inversely correlated to Bcl2 expression in CLL and that ...

Journal: :Blood 2009
Weimin Ci Jose M Polo Leandro Cerchietti Rita Shaknovich Ling Wang Shao Ning Yang Kenny Ye Pedro Farinha Douglas E Horsman Randy D Gascoyne Olivier Elemento Ari Melnick

The BCL6 transcriptional repressor is required for development of germinal center (GC) B cells and when expressed constitutively causes diffuse large B-cell lymphomas (DLBCLs). We examined genome-wide BCL6 promoter binding in GC B cells versus DLBCLs to better understand its function in these settings. BCL6 bound to both distinct and common sets of functionally related gene in normal GC cells v...

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