Evidence map›Paper›PMID 32098321›Full record

ArticleCancers2020

Small Molecule Binds with Lymphocyte Antigen 6K to Induce Cancer Cell Death.

Senyi Benti, Purushottam B Tiwari, Dustin W Goodlett, Leily Daneshian, Grant B Kern, Mark D Smith, Aykut Uren, Maksymilian Chruszcz, Linda S Shimizu, Geeta Upadhyay

Abstract read
In one paragraph

Article in Cancers, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
–field-weighted citation impact
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

11 citing papers in PubMed.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors.

Senyi BentiDepartment of Oncology, Georgetown University Medical Center, Washington, DC 20057, USA.
Purushottam B TiwariDepartment of Oncology, Georgetown University Medical Center, Washington, DC 20057, USA.
Dustin W GoodlettDepartment of Chemistry and Biochemistry, University of South Carolina, Columbia, SC 29208, USA.
Leily DaneshianDepartment of Chemistry and Biochemistry, University of South Carolina, Columbia, SC 29208, USA.
Grant B KernDepartment of Pathology, Uniformed Services University of the Health Sciences, Bethesda, MD 20814, USA.ORCID 0000-0002-6230-9877
Mark D SmithDepartment of Chemistry and Biochemistry, University of South Carolina, Columbia, SC 29208, USA.
Aykut UrenDepartment of Oncology, Georgetown University Medical Center, Washington, DC 20057, USA.
Maksymilian ChruszczDepartment of Chemistry and Biochemistry, University of South Carolina, Columbia, SC 29208, USA.ORCID 0000-0001-7521-5485
Linda S ShimizuDepartment of Chemistry and Biochemistry, University of South Carolina, Columbia, SC 29208, USA.ORCID 0000-0001-5599-4960
Geeta UpadhyayDepartment of Oncology, Georgetown University Medical Center, Washington, DC 20057, USA.

Funding

Role of Ly6K in TGF-beta and immune escape pathways of triple negative breast cancerR01CA227694 · NCI · HENRY M. JACKSON FDN FOR THE ADV MIL/MED · PI Geeta Upadhyay · 2018 to 2026
$2.4M
NCI NIH HHS R01 CA227694NIH HHS P30CA51008NIH HHS R01CA227694
6 · The paper itself

Abstract

Elevated gene expression of Lymphocyte antigen 6K (LY6K) in cancer cells is associated with poor survival outcomes in multiple different cancer types including cervical, breast, ovarian, lung, and head and neck cancer. Since inhibition of LY6K expression inhibits cancer cell growth, we set out to explore whether pharmacological inhibition of LY6K could produce the same effect. We screened small molecule libraries for direct binding to recombinant LY6K protein in a surface plasmon resonance assay. We found that NSC243928 directly binds to the full-length and mature forms of LY6K and inhibits growth of HeLa cells that express LY6K. NSC243928 did not display binding with LY6D or LY6E. Our data demonstrate a first-time proof of principle study that pharmacological inhibition of LY6K using small molecules in cancer cells is a valid approach to developing targeted therapies against LY6K. This approach will be specifically relevant in hard-to-treat cancers where LY6K is highly expressed, such as cervical, pancreatic, ovarian, head and neck, lung, gastric, and triple-negative breast cancers.

Indexed as

cervical cancerLY6KNSC243928small moleculesurface plasmon resonance

Identifiers

PMID32098321
PMCPMC7072568

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Registered trials

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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.