Evidence map›Paper›PMID 30450161›Full record

ArticleOncotarget2018

Down-regulation of AR splice variants through XPO1 suppression contributes to the inhibition of prostate cancer progression.

Amro Aboukameel, Irfana Muqbil, Erkan Baloglu, William Senapedis, Yosef Landesman, Christian Argueta, Michael Kauffman, Hua Chang, Trinayan Kashyap, Sharon Shacham and 4 more

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.5field-weighted citation impact, top 17% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

12 citing papers in PubMed, 16 citations in OpenAlex.

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  12. FOXA1 in prostate cancer.Asian journal of andrology
    Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

14 authors at 4 institutions in 2 countries.

Amro AboukameelWayne State University School of Medicine, Detroit, MI, USA.
Irfana MuqbilUniversity of Detroit Mercy, Detroit, MI, USA.
Erkan BalogluKaryopharm Therapeutics Inc, Newton, MA, USA.
William SenapedisKaryopharm Therapeutics Inc, Newton, MA, USA.
Yosef LandesmanKaryopharm Therapeutics Inc, Newton, MA, USA.
Christian ArguetaKaryopharm Therapeutics Inc, Newton, MA, USA.
Michael KauffmanKaryopharm Therapeutics Inc, Newton, MA, USA.
Hua ChangKaryopharm Therapeutics Inc, Newton, MA, USA.
Trinayan KashyapKaryopharm Therapeutics Inc, Newton, MA, USA.
Sharon ShachamKaryopharm Therapeutics Inc, Newton, MA, USA.
Jasper E NeggersKU Leuven Department of Microbiology and Immunology, Laboratory of Virology and Chemotherapy, Rega Institute for Medical Research, Herestraat, Belgium.
Dirk DaelemansKU Leuven Department of Microbiology and Immunology, Laboratory of Virology and Chemotherapy, Rega Institute for Medical Research, Herestraat, Belgium.
Elisabeth I HeathWayne State University School of Medicine, Detroit, MI, USA.
Asfar S AzmiWayne State University School of Medicine, Detroit, MI, USA.
Karyopharm Therapeutics (United States) · USWayne State University · USRega Institute for Medical Research · BEUniversity of Detroit Mercy · US

Funding

Clinical Translation of Nuclear Export Inhibitor in Metastatic Pancreatic CancerR37CA215427 · NCI · WAYNE STATE UNIVERSITY · PI AZMI, ASFAR S · 2018 to 2024
$2.4M
NCI NIH HHS R37 CA215427
6 · The paper itself

Abstract

Emerging studies have shown that the expression of AR splice variants (ARv) lacking ligand-binding domain is associated with castrate-resistant prostate cancer (CRPC) and higher risk of tumor metastasis and recurrence. Nuclear export protein XPO1 regulates the nuclear localization of many proteins including tumor suppressor proteins. Increased XPO1 in prostate cancer is associated with a high Gleason score and bone metastasis. In this study, we found that high expression of AR splice variant 7 (AR-v7) was correlated with increased XPO1 expression. Silencing of XPO1 by RNAi or treatment with Selective Inhibitor of Nuclear Export (SINE) compounds selinexor and eltanexor (KPT-8602) down-regulated the expression of AR, AR-v7 and ARv567es at mRNA and protein levels. XPO1 silencing also inhibited the expression of AR and ARv regulators including FOXA1, Src, Vav3, MED1 and Sam68, leading to the suppression of ARv and AR target genes, UBE2C and PSA. By targeting XPO1/ARv signaling, SINE suppressed prostate cancer (PCa) growth

Indexed as

AR SPLICE variantCRM1metastatic prostate cancernuclear exportSINE

Identifiers

PMID30450161
PMCPMC6219671
OpenAlexW2895933654

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.