XPO1 expression worsens the prognosis of unfavorable DLBCL that can be effectively targeted by selinexor in the absence of mutant p53.
Antineoplastic Agents
/ therapeutic use
Cell Line, Tumor
Gene Expression Regulation, Neoplastic
/ drug effects
Humans
Hydrazines
/ therapeutic use
Karyopherins
/ antagonists & inhibitors
Lymphoma, Large B-Cell, Diffuse
/ diagnosis
Prognosis
Receptors, Cytoplasmic and Nuclear
/ antagonists & inhibitors
Triazoles
/ therapeutic use
Tumor Suppressor Protein p53
/ genetics
Exportin 1 Protein
BCL2
DLBCL
HGBCL
MYC
Selinexor
TP53 mutation
XPO1
Journal
Journal of hematology & oncology
ISSN: 1756-8722
Titre abrégé: J Hematol Oncol
Pays: England
ID NLM: 101468937
Informations de publication
Date de publication:
04 11 2020
04 11 2020
Historique:
received:
19
09
2020
accepted:
22
10
2020
entrez:
5
11
2020
pubmed:
6
11
2020
medline:
8
6
2021
Statut:
epublish
Résumé
The XPO1 inhibitor selinexor was recently approved in relapsed/refractory DLBCL patients but only demonstrated modest anti-DLBCL efficacy, prompting us to investigate the prognostic effect of XPO1 in DLBCL patients and the rational combination therapies in high-risk DLBCL. High XPO1 expression (XPO1
Identifiants
pubmed: 33148342
doi: 10.1186/s13045-020-00982-3
pii: 10.1186/s13045-020-00982-3
pmc: PMC7641823
doi:
Substances chimiques
Antineoplastic Agents
0
Hydrazines
0
Karyopherins
0
Receptors, Cytoplasmic and Nuclear
0
Triazoles
0
Tumor Suppressor Protein p53
0
selinexor
31TZ62FO8F
Types de publication
Letter
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
148Subventions
Organisme : NCI NIH HHS
ID : P30 CA014236
Pays : United States
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