FOXM1 Modulates Treatment Outcomes in Acute Myeloid Leukemia

I Khan - 2020 - search.proquest.com
Abstract Acute Myeloid Leukemia (AML) patients with NPM1 mutations, known to cause
aberrant cytoplasmic re-localization, demonstrate a superior response to standard …

[HTML][HTML] FOXM1 contributes to treatment failure in acute myeloid leukemia

I Khan, M Halasi, A Patel, R Schultz, N Kalakota… - JCI insight, 2018 - ncbi.nlm.nih.gov
Acute myeloid leukemia (AML) patients with NPM1 mutations demonstrate a superior
response to standard chemotherapy treatment. Our previous work has shown that these …

[HTML][HTML] FOXM1 Mediates Drug-Resistance and Represents a Therapeutic Target in Pre-B Acute Lymphoblastic Leukemia

M Buchner, E Park, L Klemm, H Geng, D Kopanja… - Blood, 2014 - Elsevier
Abstract Background & Significance: Pre-B acute lymphoblastic leukemia (ALL) emerges in
virtually all cases from B cell precursors that are arrested at the pre-B cell receptor …

FOXM1 is overexpressed in B-acute lymphoblastic leukemia (B-ALL) and its inhibition sensitizes B-ALL cells to chemotherapeutic drugs

F Consolaro, G Basso… - International …, 2015 - spandidos-publications.com
The Forkhead box protein M1 (FOXM1) is a transcription factor that plays a central role in the
regulation of cell cycle, proliferation, DNA repair, and apoptosis. FOXM1 is overexpressed in …

[HTML][HTML] Validation of FOXM1 As a Therapeutic Target in Acute Myeloid Leukemia

I Khan, AA Patel, M Halasi, R Schultz, YH Chen… - Blood, 2017 - Elsevier
Abstract Objectives: Forkhead box M1 (FOXM1) is a transcription factor of the Forkhead
family that induces genes critical in executing the mitotic program. The FOXM1 regulatory …

Favorable outcomes of NPM1mut AML patients are due to transcriptional inactivation of FOXM1, presenting a new target to overcome chemoresistance

I Khan, A Kaempf, S Raghuwanshi, M Chesnokov… - Blood cancer …, 2023 - nature.com
Acute Myeloid Leukemia (AML) is a highly heterogeneous disease with 3-year patient
survival ranging from 30 to 80%, depending on molecular characteristics. Mutations in …

Identification of FOXM1 as a therapeutic target in B-cell lineage acute lymphoblastic leukaemia

M Buchner, E Park, H Geng, L Klemm, J Flach… - Nature …, 2015 - nature.com
Despite recent advances in the cure rate of acute lymphoblastic leukaemia (ALL), the
prognosis for patients with relapsed ALL remains poor. Here we identify FOXM1 as a …

Abstract A09: Targeting of FOXM1 recapitulates NPM1 mutations in chemo-sensitization of AML

I Khan, S Raghuwanshi, A Kaempf, J Tyner… - Blood Cancer …, 2023 - AACR
NPM1 mutations are among the most common mutations in CN-AML (Cytogenetically
Normal-AML) and are known to enhance chemosensitivity in AML patients. Across multiple …

[HTML][HTML] FOXM1-AKT positive regulation loop provides venetoclax resistance in AML

MS Chesnokov, S Borhani, M Halasi, Z Arbieva… - Frontiers in …, 2021 - frontiersin.org
Forkhead box protein M1 (FOXM1) is a crucial regulator of cancer development and
chemoresistance. It is often overexpressed in acute myeloid leukemia (AML) and is …

[HTML][HTML] FOXO1 is involved in the regulation of B-cell precursor acute lymphoblastic leukemia survival and serves as a novel target for directed therapy

S Demir, F Wang, F Gehringer, C Weitzer, KM Debatin… - Blood, 2016 - Elsevier
Acute lymphoblastic leukemia (ALL) is the most common pediatric and adolescent
malignancy. Although current treatment provides five-year event-free survival, in up to 20 …