Projects funded by the NCN


Information on the principal investigator and host institution

Information of the project and the call

Keywords

Equipment

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Association of the constitutional DNA double strand breaks repair with specific molecular features of diffuse large B-cell lymphoma in Nijmegen syndrome

2017/26/D/NZ5/00811

Keywords:

Nijmegen breakage syndrome genes diffuse large B-cell lymphoma

Descriptors:

  • NZ5_3: Pathogenesis of human diseases
  • NZ2_1: Molecular genetics

Panel:

NZ5 - Human and animal noninfectious diseases: etiology, mechanisms, diagnosis and treatment of diseases, poisonings and injuries (without neurological diseases)

Host institution :

Uniwersytet Medyczny w Łodzi, Wydział lekarski

woj. łódzkie

Other projects carried out by the institution 

Principal investigator (from the host institution):

dr Agata Pastorczak 

Number of co-investigators in the project: 3

Call: SONATA 13 - announced on 2017-06-14

Amount awarded: 614 600 PLN

Project start date (Y-m-d): 2018-04-17

Project end date (Y-m-d): 2021-10-16

Project duration:: 42 months (the same as in the proposal)

Project status: Project settled

Project description

Download the project description in a pdf file

Note - project descriptions were prepared by the authors of the applications themselves and placed in the system in an unchanged form.

Equipment purchased [PL]

  1. -.

Information in the final report

  • Publication in academic press/journals (4)
  1. Consensus Recommendations for the Clinical Management of Hematological Malignancies in Patients with DNA Double Stranded Break Disorders
    Authors:
    Pastorczak A, Attarbaschi A, Bomken S, Borkhardt A, van der Werff Ten Bosch J, Elitzur S, Gennery AR, Hlavackova E, Kerekes A, Křenová Z, Mlynarski W, Szczepanski T, Wassenberg T, Loeffen J.
    Academic press:
    Cancers (rok: 2022, tom: 14, strony: 45314), Wydawca: MDPI
    Status:
    Published
    DOI:
    10.3390/cancers14082000 - link to the publication
  2. Genetic predisposition to lymphomas: overview of rare syndromes and inherited familial variants  
    Authors:
    Bartosz Szmyd, Wojciech Mlynarski, Agata Pastorczak
    Academic press:
    Mutation Research-Reviews in Mutation Research (rok: 2021, tom: brak, strony: brak), Wydawca: Elsevier
    Status:
    Published
    DOI:
    10.1016/j.mrrev.2021.108386 - link to the publication
  3. Hematopoietic Stem Cell Transplantation Positively Affects the Natural History of Cancer in Nijmegen Breakage Syndrome
    Authors:
    Beata Wolska-Kusnierz , Agata Pastorczak, Wojciech Fendler , Anna Wakulinska, Bozena Dembowska-Baginska, Edyta Heropolitanska-Pliszka, Barbara Piątos, Barbara Pietrucha, Krzysztof Kałwak, Marek Ussowicz, Anna Pieczonka, Katarzyna Drabko, Monika Lejman, Sylwia Koltan, Jolanta Gozdzik, Jan Styczynski, Alina Fedorova, Natalia Miakova, Elena Deripapa, Larysa Kostyuchenko, Zdenka Krenova, Eva Hlavackova, Andrew R Gennery, Karl-Walter Sykora, Sujal Ghosh, Michael H Albert, Dmitry Balashov, Mary Eapen, Peter Svec, Markus G Seidel, Sara S Kilic, Agnieszka Tomaszewska, Ewa Wiesik-Szewczyk, Alexandra Kreins, Johann Greil, Jochen Buechner, Bendik Lund, Hanna Gregorek , Krystyna Chrzanowska, Wojciech Mlynarski
    Academic press:
    Clinical Cancer Research (rok: 2021, tom: 27, strony: 575-584), Wydawca: AACR Journals
    Status:
    Published
    DOI:
    10.1158/1078-0432.CCR-20-2574. - link to the publication
  4. Clinical and laboratory diversity of diffuse large B-cell lymphomas in children with Nijmegen breakage syndrome
    Authors:
    Pastorczak A, Szmyd B, Braun M, Madzio J, Wypyszczak K, Sztromwasser P, Fendler W, Wojtaszewska M, Chrzanowski J, Grajkowska W, Gregorek H, Wakulinska A, Kazanowska B, Krenova Z, Weijers DD, Kuiper RP, Mlynarski W.
    Academic press:
    Haematologica (rok: 2023, tom: brak, strony: brak), Wydawca: Ferrata-Storti Foundation
    Status:
    Published
    DOI:
    10.3324/haematol.2022.282325 - link to the publication