Nucleo-cytoplasmic transport as a therapeutic target of cancer

GL Gravina, W Senapedis, D McCauley… - Journal of hematology & …, 2014 - Springer
Shuttling of specific proteins out of the nucleus is essential for the regulation of the cell cycle
and proliferation of both normal and malignant tissues. Dysregulation of this fundamental …

Nuclear export of proteins and drug resistance in cancer

JG Turner, J Dawson, DM Sullivan - Biochemical pharmacology, 2012 - Elsevier
The intracellular location of a protein is crucial to its normal functioning in a cell. Cancer cells
utilize the normal processes of nuclear-cytoplasmic transport through the nuclear pore …

[HTML][HTML] Oral selinexor–dexamethasone for triple-class refractory multiple myeloma

A Chari, DT Vogl, M Gavriatopoulou… - … England Journal of …, 2019 - Mass Medical Soc
Background Selinexor, a selective inhibitor of nuclear export compound that blocks exportin
1 (XPO1) and forces nuclear accumulation and activation of tumor suppressor proteins …

Genomic and molecular characterization of esophageal squamous cell carcinoma

DC Lin, JJ Hao, Y Nagata, L Xu, L Shang, X Meng… - Nature …, 2014 - nature.com
Esophageal squamous cell carcinoma (ESCC) is prevalent worldwide and particularly
common in certain regions of Asia. Here we report the whole-exome or targeted deep …

A novel circular RNA, circXPO1, promotes lung adenocarcinoma progression by interacting with IGF2BP1

Q Huang, H Guo, S Wang, Y Ma, H Chen, H Li… - Cell death & …, 2020 - nature.com
Studies have demonstrated that noncoding RNAs play important roles in various types of
cancer; however, noncoding RNAs derived from regions of genomic alterations have rarely …

Selective inhibitors of nuclear export show that CRM1/XPO1 is a target in chronic lymphocytic leukemia

R Lapalombella, Q Sun, K Williams… - Blood, The Journal …, 2012 - ashpublications.org
The nuclear export protein XPO1 is overexpressed in cancer, leading to the cytoplasmic
mislocalization of multiple tumor suppressor proteins. Existing XPO1-targeting agents lack …

First-in-class, first-in-human phase I study of selinexor, a selective inhibitor of nuclear export, in patients with advanced solid tumors

AR Abdul Razak, M Mau-Soerensen… - Journal of Clinical …, 2016 - ascopubs.org
Purpose This trial evaluated the safety, pharmacokinetics, pharmacodynamics, and efficacy
of selinexor (KPT-330), a novel, oral small-molecule inhibitor of exportin 1 (XPO1/CRM1) …

CRM1 inhibition induces tumor cell cytotoxicity and impairs osteoclastogenesis in multiple myeloma: molecular mechanisms and therapeutic implications

YT Tai, Y Landesman, C Acharya, Y Calle, MY Zhong… - Leukemia, 2014 - nature.com
The key nuclear export protein CRM1/XPO1 may represent a promising novel therapeutic
target in human multiple myeloma (MM). Here we showed that chromosome region …

Selective inhibition of nuclear export with oral selinexor for treatment of relapsed or refractory multiple myeloma

DT Vogl, D Dingli, RF Cornell, CA Huff… - Journal of clinical …, 2018 - ascopubs.org
Purpose Selinexor, a first-in-class, oral, selective exportin 1 (XPO1) inhibitor, induces
apoptosis in cancer cells through nuclear retention of tumor suppressor proteins and the …

Proteomic profiling of exosomes leads to the identification of novel biomarkers for prostate cancer

D Duijvesz, KE Burnum-Johnson, MA Gritsenko… - PloS one, 2013 - journals.plos.org
Background Current markers for prostate cancer, such as PSA lack specificity. Therefore,
novel biomarkers are needed. Unfortunately, the complexity of body fluids often hampers …