Evidence map›Paper›PMID 24936214›Full record

ArticleAmerican journal of translational research2014

Small cell lung cancer cells express the late stage gBK tumor antigen: a possible immunotarget for the terminal disease.

Neil T Hoa, Lisheng Ge, Rajeev B Tajhya, Christine Beeton, Andrew N Cornforth, Amir Abolhoda, Nils Lambrecht, Maria DaCosta-Iyer, Yi Ouyang, Anthony P Mai and 6 more

Open access · greenAbstract read
In one paragraph

Article in American journal of translational research, 2014. 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
1.3field-weighted citation impact, top 20% 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, 17 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Article
  5. Advances and challenges in immunotherapy of small cell lung cancer.Chinese journal of cancer research = Chung-kuo yen cheng yen chiu · 2020
    Article
  6. Review
  7. Article
  8. Large conductance voltage and CaAmerican journal of translational research · 2017
    Article
  9. Targeting Btk with ibrutinib inhibit gastric carcinoma cells growth.American journal of translational research · 2016
    Article
  10. Article
  11. Article
  12. Review
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

16 authors at 1 institution in 1 country.

Neil T HoaResearch Health Care Group, Veterans Affairs Medical Center Long Beach, CA 90822, USA.
Lisheng GeResearch Health Care Group, Veterans Affairs Medical Center Long Beach, CA 90822, USA.
Rajeev B TajhyaDepartment of Molecular Physiology and Biophysics, Baylor College of Medicine Houston, Texas 77030, USA.
Christine BeetonDepartment of Molecular Physiology and Biophysics, Baylor College of Medicine Houston, Texas 77030, USA.
Andrew N CornforthCalifornia Stem Cell Inc. 18301 Von Karman Ave, Irvine, CA 92612, USA.
Amir AbolhodaSurgical Health Care Group, Veterans Affairs Medical Center Long Beach, CA 90822, USA.
Nils LambrechtPathology and Laboratory Medicine Service, Veterans Affairs Medical Center Long Beach, CA 90822, USA ; Department of Pathology and Laboratory Medicine, University of California Irvine, Orange, CA 92868, USA.
Maria DaCosta-IyerPathology and Laboratory Medicine Service, Veterans Affairs Medical Center Long Beach, CA 90822, USA ; Department of Pathology and Laboratory Medicine, University of California Irvine, Orange, CA 92868, USA.
Yi OuyangPathology and Laboratory Medicine Service, Veterans Affairs Medical Center Long Beach, CA 90822, USA ; Department of Pathology and Laboratory Medicine, University of California Irvine, Orange, CA 92868, USA.
Anthony P MaiResearch Health Care Group, Veterans Affairs Medical Center Long Beach, CA 90822, USA.
Erin HongResearch Health Care Group, Veterans Affairs Medical Center Long Beach, CA 90822, USA.
Judy ShonResearch Health Care Group, Veterans Affairs Medical Center Long Beach, CA 90822, USA.
Michelle J HickeyDepartment of Neurosurgery, David Geffen School of Medicine, University of California Los Angeles, Los Angeles, CA 90095, USA.
Kate L EricksonDepartment of Neurosurgery, David Geffen School of Medicine, University of California Los Angeles, Los Angeles, CA 90095, USA.
Carol A KruseDepartment of Neurosurgery, David Geffen School of Medicine, University of California Los Angeles, Los Angeles, CA 90095, USA.
Martin R JadusResearch Health Care Group, Veterans Affairs Medical Center Long Beach, CA 90822, USA ; Pathology and Laboratory Medicine Service, Veterans Affairs Medical Center Long Beach, CA 90822, USA ; Department of Pathology and Laboratory Medicine, University of California Irvine, Orange, CA 92868, USA ; Neuro-Oncology Program, Chao Comprehensive Cancer Center, University of California Irvine, Orange, CA 92868, USA.
University of California, Los Angeles · US

Funding

Adoptive Transfer of AlloCTL for Immunotherapy of Recurrent GliomasR01CA125244 · NCI · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI LIAU, LINDA M · 2010 to 2014
$2.4M
Optimizing Induction Conditions for Immunotherapeutic CTLR01CA154256 · NCI · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI PRINS, ROBERT M · 2010 to 2014
$1.9M
NCI NIH HHS R01 CA125244NCI NIH HHS R01 CA154256
6 · The paper itself

Abstract

Big Potassium (BK) ion channels have several splice variants. One splice variant initially described within human glioma cells is called the glioma BK channel (gBK). Using a gBK-specific antibody, we detected gBK within three human small cell lung cancer (SCLC) lines. Electrophysiology revealed that functional membrane channels were found on the SCLC cells. Prolonged exposure to BK channel activators caused the SCLC cells to swell within 20 minutes and resulted in their death within five hours. Transduction of BK-negative HEK cells with gBK produced functional gBK channels. Quantitative RT-PCR analysis using primers specific for gBK, but not with a lung-specific marker, Sox11, confirmed that advanced, late-stage human SCLC tissues strongly expressed gBK mRNA. Normal human lung tissue and early, lower stage SCLC resected tissues very weakly expressed this transcript. Immunofluorescence using the anti-gBK antibody confirmed that SCLC cells taken at the time of the autopsy intensely displayed this protein. gBK may represent a late-stage marker for SCLC. HLA-A*0201 restricted human CTL were generated in vitro using gBK peptide pulsed dendritic cells. The exposure of SCLC cells to interferon-γ (IFN-γ) increased the expression of HLA; these treated cells were killed by the CTL better than non-IFN-γ treated cells even though the IFN-γ treated SCLC cells displayed diminished gBK protein expression. Prolonged incubation with recombinant IFN-γ slowed the in vitro growth and prevented transmigration of the SCLC cells, suggesting IFN-γ might inhibit tumor growth in vivo. Immunotherapy targeting gBK might impede advancement to the terminal stage of SCLC via two pathways.

Indexed as

BK ion channelCTLsglioma BK ion channelinterferon-γreal time PCRSmall cell lung cancer

Identifiers

PMID24936214
PMCPMC4058303
OpenAlexW166465745

What OpenQuestion holds

Textmetadata
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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.