Results 21 to 30 of about 5,881 (166)

Exportin 1‐mediated nuclear/cytoplasmic trafficking controls drug sensitivity of classical Hodgkin's lymphoma

open access: yesMolecular Oncology, 2023
Exportin 1 (XPO1) is the main nuclear export receptor that controls the subcellular trafficking and the functions of major regulatory proteins. XPO1 is overexpressed in various cancers and small inhibitors of nuclear export (SINEs) have been developed to
Mélody Caillot   +10 more
doaj   +1 more source

Protein biomarkers for response to XPO1 inhibition in hematologic malignancies

open access: yesJournal of Cellular and Molecular Medicine, 2022
Abstract XPO1 (Exportin-1) is the nuclear export protein responsible for the normal shuttling of several proteins and RNA species between the nucleocytoplasmic compartment of eukaryotic cells. XPO1 recognizes the nuclear export signal (NES) of its cargo proteins to facilitate its export.
Tulasigeri M. Totiger   +9 more
openaire   +2 more sources

XPO1/CRM1 is a promising prognostic indicator for neuroblastoma and represented a therapeutic target by selective inhibitor verdinexor

open access: yesJournal of Experimental & Clinical Cancer Research, 2021
Background High-risk neuroblastoma patients have a 5-year survival rate of less than 50%. It’s an urgent need to identify new therapeutic targets and the appropriate drugs.
Lijia Pan   +5 more
doaj   +1 more source

XPO1, therapeutic...and prognostic target in sarcomas

open access: yesOncoscience, 2016
In a recent issue of Oncotarget [1], Nakayama et al. showed the anti-tumor activity of selinexor, an inhibitor of exportin 1, against a wide variety of sarcoma preclinical models, including several pathological subtypes of soft tissue sarcomas (STS).
Bertucci, François   +2 more
openaire   +3 more sources

Azacitidine Is Synergistically Lethal with XPO1 Inhibitor Selinexor in Acute Myeloid Leukemia by Targeting XPO1/eIF4E/c-MYC Signaling

open access: yesInternational Journal of Molecular Sciences, 2023
Acute myeloid leukemia (AML) is a high-mortality malignancy with poor outcomes. Azacitidine induces cell death and demonstrates treatment effectiveness against AML. Selinexor (KPT-330) exhibited significant benefits in combination with typical induction treatment for AML patients.
Huideng Long   +4 more
openaire   +2 more sources

Inhibition of XPO-1 Mediated Nuclear Export through the Michael-Acceptor Character of Chalcones

open access: yesPharmaceuticals, 2021
The nuclear export receptor exportin-1 (XPO1, CRM1) mediates the nuclear export of proteins that contain a leucine-rich nuclear export signal (NES) towards the cytoplasm.
Marta Gargantilla   +6 more
doaj   +1 more source

Formation of a Trimeric Xpo1-Ran[GTP]-Ded1 Exportin Complex Modulates ATPase and Helicase Activities of Ded1.

open access: yesPLoS ONE, 2015
The DEAD-box RNA helicase Ded1, which is essential in yeast and known as DDX3 in humans, shuttles between the nucleus and cytoplasm and takes part in several basic processes including RNA processing and translation.
Glenn Hauk, Gregory D Bowman
doaj   +1 more source

Give me a SINE: how Selective Inhibitors of Nuclear Export modulate autophagy and aging

open access: yesMolecular & Cellular Oncology, 2018
Autophagy is a cellular recycling process leading to lysosomal degradation of damaged macromolecules, which can protect cells against aging. The transcription factor EB (TFEB), a major transcriptional regulator of genes involved in autophagy and ...
A.V. Kumar   +5 more
doaj   +1 more source

Preclinical activity of selinexor, an inhibitor of XPO1, in sarcoma

open access: yesOncotarget, 2016
Selinexor is an orally bioavailable selective inhibitor of nuclear export that has been demonstrated to have preclinical activity in various cancer types and that is currently in Phase I and II clinical trials for advanced cancers. In this study, we evaluated the effects of selinexor in several preclinical models of various sarcoma subtypes.
Nakayama, Robert   +7 more
openaire   +5 more sources

Simultaneous targeting of XPO1 and BCL2 as an effective treatment strategy for double-hit lymphoma

open access: yesJournal of Hematology & Oncology, 2019
Double-hit lymphoma (DHL) is among the most aggressive and chemoresistant lymphoma subtypes. DHLs carry genomic abnormalities in MYC, BCL2, and/or BCL6 oncogenes. Due to the simultaneous overexpression of these driver oncogenes, DHLs are highly resistant
Yuanhui Liu   +4 more
doaj   +1 more source

Home - About - Disclaimer - Privacy