Literature DB >> 32511022

Selinexor: a first-in-class SINE compound for treatment of relapsed refractory multiple myeloma.

Shambavi Richard1, Joshua Richter1, Sundar Jagannath1.   

Abstract

The progression of multiple myeloma is accompanied by complex cytogenetic and epigenetic alterations that include mutation or functional inactivation of tumor suppressor proteins and overexpression of oncoproteins. Patients whose myeloma is refractory to the three major classes of drugs including immunomodulatory agents, proteasome inhibitors and anti-CD38 monoclonal antibodies have a very poor prognosis. Drugs with novel mechanisms of action that can bypass resistance mechanisms are sorely needed for this group of patients. Selinexor represents a novel, oral agent with an innovative mechanism of action that offers a significant therapeutic advance in this group of heavily treated patients. Moreover, this novel mechanism may provide additional options for patients with less refractory disease.

Entities:  

Keywords:  SINE; XPO1; exportin 1; karyopherin; multiple myeloma; refractory; relapsed; selective inhibitor of nuclear export; selinexor

Mesh:

Substances:

Year:  2020        PMID: 32511022     DOI: 10.2217/fon-2020-0054

Source DB:  PubMed          Journal:  Future Oncol        ISSN: 1479-6694            Impact factor:   3.404


  2 in total

Review 1.  Pathogenesis and treatment of multiple myeloma.

Authors:  Peipei Yang; Ying Qu; Mengyao Wang; Bingyang Chu; Wen Chen; Yuhuan Zheng; Ting Niu; Zhiyong Qian
Journal:  MedComm (2020)       Date:  2022-06-02

2.  Targeted CRM1-inhibition perturbs leukemogenic NUP214 fusion proteins and exerts anti-cancer effects in leukemia cell lines with NUP214 rearrangements.

Authors:  Adélia Mendes; Ramona Jühlen; Valérie Martinelli; Birthe Fahrenkrog
Journal:  Oncotarget       Date:  2020-09-08
  2 in total

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