BCOR involvement in cancer

A Astolfi, M Fiore, F Melchionda, V Indio… - …, 2019 - Taylor & Francis
BCOR is a gene that encodes for an epigenetic regulator involved in the specification of cell
differentiation and body structure development and takes part in the noncanonical polycomb …

Molecular map of chronic lymphocytic leukemia and its impact on outcome

BA Knisbacher, Z Lin, CK Hahn, F Nadeu… - Nature …, 2022 - nature.com
Recent advances in cancer characterization have consistently revealed marked
heterogeneity, impeding the completion of integrated molecular and clinical maps for each …

[HTML][HTML] MYD88 in the driver's seat of B-cell lymphomagenesis: From molecular mechanisms to clinical implications

RAL de Groen, AMR Schrader, MJ Kersten… - …, 2019 - ncbi.nlm.nih.gov
More than 50 subtypes of B-cell non-Hodgkin lymphoma (B-NHL) are recognized in the most
recent World Health Organization classification of 2016. The current treatment paradigm …

Venetoclax plus rituximab in relapsed chronic lymphocytic leukemia: 4-year results and evaluation of impact of genomic complexity and gene mutations from the …

AP Kater, JQ Wu, T Kipps, B Eichhorst… - Journal of Clinical …, 2020 - ascopubs.org
PURPOSE In previous analyses of the MURANO study, fixed-duration venetoclax plus
rituximab (VenR) resulted in improved progression-free survival (PFS) compared with …

Spliceosomal disruption of the non-canonical BAF complex in cancer

D Inoue, GL Chew, B Liu, BC Michel, J Pangallo… - Nature, 2019 - nature.com
SF3B1 is the most commonly mutated RNA splicing factor in cancer,,–, but the mechanisms
by which SF3B1 mutations promote malignancy are poorly understood. Here we integrated …

Altered RNA splicing by mutant p53 activates oncogenic RAS signaling in pancreatic cancer

LF Escobar-Hoyos, A Penson, R Kannan, H Cho… - Cancer cell, 2020 - cell.com
Pancreatic ductal adenocarcinoma (PDAC) is driven by co-existing mutations in KRAS and
TP53. However, how these mutations collaborate to promote this cancer is unknown. Here …

[HTML][HTML] Genomic arrays identify high-risk chronic lymphocytic leukemia with genomic complexity: a multicenter study

AC Leeksma, P Baliakas, T Moysiadis, A Puiggros… - …, 2021 - ncbi.nlm.nih.gov
Complex karyotype identified by chromosome-banding analysis has been shown to have
prognostic value in chronic lymphocytic leukemia (CLL). Genomic arrays offer high …

Dissection of subclonal evolution by temporal mutation profiling in chronic lymphocytic leukemia patients treated with ibrutinib

A Gángó, D Alpár, B Galik, D Marosvári… - … Journal of Cancer, 2020 - Wiley Online Library
The Bruton's tyrosine kinase (BTK) inhibitor ibrutinib is inducing durable responses in
chronic lymphocytic leukemia (CLL) patients with refractory/relapsed disease or with TP53 …

Clinical significance of TP53, BIRC3, ATM and MAPK-ERK genes in chronic lymphocytic leukaemia: data from the randomised UK LRF CLL4 trial

SJ Blakemore, R Clifford, H Parker, P Antoniou… - Leukemia, 2020 - nature.com
Despite advances in chronic lymphocytic leukaemia (CLL) treatment, globally chemotherapy
remains a central treatment modality, with chemotherapy trials representing an invaluable …

SF3B1 mutation–mediated sensitization to H3B-8800 splicing inhibitor in chronic lymphocytic leukemia

I López-Oreja, A Gohr, H Playa-Albinyana… - Life Science …, 2023 - life-science-alliance.org
Splicing factor 3B subunit 1 (SF3B1) is involved in pre-mRNA branch site recognition and is
the target of antitumor-splicing inhibitors. Mutations in SF3B1 are observed in 15% of …