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2.
Am J Hematol ; 94(1): E35-E37, 2019 01.
Article in English | MEDLINE | ID: mdl-30370955
3.
Blood Rev ; 46: 100758, 2021 03.
Article in English | MEDLINE | ID: mdl-32972802

ABSTRACT

Exportin 1 (XPO1), also known as chromosome maintenance 1 protein (CRM1), is the main transporter for hundreds of proteins like tumor suppressors, growth regulatory factors, oncoprotein mRNAs and others. Its upregulation leads to the inactivation of the tumor suppressor anti-neoplastic function in many cancers and logically is associated with poor prognosis. Selective inhibitors of nuclear export (SINE) are a new generation of XPO1 inhibitors that are being investigated as a promising targeted anti-cancer therapy. Selinexor is the first generation of SINE compounds that is being evaluated in many clinical trials involving solid tumors and hematological malignancies with its two approved indications for relapsed multiple myeloma and relapsed diffuse large B-cell lymphoma. Here, we comprehensively review the current knowledge of selinexor and next generations of the SINE compounds in lymphoid and myeloid malignancies.


Subject(s)
Active Transport, Cell Nucleus/drug effects , Antineoplastic Agents/pharmacology , Hydrazines/pharmacology , Triazoles/pharmacology , Antineoplastic Agents/therapeutic use , Disease Management , Hematologic Neoplasms/diagnosis , Hematologic Neoplasms/drug therapy , Hematologic Neoplasms/etiology , Hematologic Neoplasms/mortality , Humans , Hydrazines/therapeutic use , Karyopherins/antagonists & inhibitors , Molecular Targeted Therapy , Prognosis , Receptors, Cytoplasmic and Nuclear/antagonists & inhibitors , Treatment Outcome , Triazoles/therapeutic use , Exportin 1 Protein
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