Evidence map›Paper›PMID 29622795›Full record

ArticleOncogene2018

Antitumor activity of CD56-chimeric antigen receptor T cells in neuroblastoma and SCLC models.

Denise L Crossland, Warren L Denning, Sonny Ang, Simon Olivares, Tiejuan Mi, Kirsten Switzer, Harjeet Singh, Helen Huls, Kate S Gold, Bonnie S Glisson and 2 more

Abstract read
PubMed Publisher
In one paragraph

Article in Oncogene, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 44 papers.

0numbers the graph read from it
0cells of the map it votes in
44citing papers in PubMed
2.4field-weighted citation impact, top 9% 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

44 citing papers in PubMed, 65 citations in OpenAlex.

  1. Article
  2. CAR-T cell immunotherapy in rhabdomyosarcoma.Journal of translational medicine · 2026
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  9. Advances in adoptive cell therapies in small cell lung cancer.Exploration of targeted anti-tumor therapy · 2025
    Review
  10. Review
  11. Review
  12. Review
  13. Article
  14. YAP1 Status Defines Two Intrinsic Subtypes of LCNEC with Distinct Molecular Features and Therapeutic Vulnerabilities.Clinical cancer research : an official journal of the American Association for Cancer Research · 2024
    Article
  15. Review
  16. Review
  17. Review
  18. Review
  19. Article
  20. 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

12 authors at 3 institutions in 1 country.

Denise L CrosslandDivision of Pediatrics, UT MD Anderson Cancer Center, Houston, TX, USA.
Warren L DenningThoracic Head and Neck Medical Oncology, UT MD Anderson Cancer Center, Houston, TX, USA.
Sonny AngStem Cell Transplantation, UT MD Anderson Cancer Center, Houston, TX, USA.
Simon OlivaresDivision of Pediatrics, UT MD Anderson Cancer Center, Houston, TX, USA.
Tiejuan MiDivision of Pediatrics, UT MD Anderson Cancer Center, Houston, TX, USA.
Kirsten SwitzerDivision of Pediatrics, UT MD Anderson Cancer Center, Houston, TX, USA.
Harjeet SinghDivision of Pediatrics, UT MD Anderson Cancer Center, Houston, TX, USA.
Helen HulsDivision of Pediatrics, UT MD Anderson Cancer Center, Houston, TX, USA.
Kate S GoldMoores Cancer Center, University of California, San Diego, La Jolla, CA, USA.
Bonnie S GlissonThoracic Head and Neck Medical Oncology, UT MD Anderson Cancer Center, Houston, TX, USA.
Laurence J CooperDivision of Pediatrics, UT MD Anderson Cancer Center, Houston, TX, USA.
John V HeymachThoracic Head and Neck Medical Oncology, UT MD Anderson Cancer Center, Houston, TX, USA. jheymach@mdanderson.org.
The University of Texas MD Anderson Cancer Center · USUniversity of California, San Diego · USZiopharm Oncology (United States) · US

Funding

NIH HHS CA00632NIH HHS CA100632NIH HHS CA136411NIH HHS CA16672NIH HHS PO1 CA148600NIH HHS RO1 CA120956NIH HHS RO1 CA124782NIH HHS RO1 CA141303
6 · The paper itself

Abstract

The CD56 antigen (NCAM-1) is highly expressed on several malignancies with neuronal or neuroendocrine differentiation, including small-cell lung cancer and neuroblastoma, tumor types for which new therapeutic options are needed. We hypothesized that CD56-specific chimeric antigen receptor (CAR) T cells could target and eliminate CD56-positive malignancies. Sleeping Beauty transposon-generated CD56R-CAR T cells exhibited αβT-cell receptors, released antitumor cytokines upon co-culture with CD56

Indexed as

AnimalsCD56 AntigenCell Line, TumorGliomaHumansLung NeoplasmsLymphocyte ActivationMiceMice, Inbred NODMice, NudeNeuroblastomaReceptors, Chimeric AntigenSmall Cell Lung CarcinomaT-LymphocytesTransposasesXenograft Model Antitumor AssaysCD56 AntigenNCAM1 protein, humanReceptors, Chimeric Antigensleeping beauty transposase, humanTransposases

Identifiers

PMID29622795
OpenAlexW2795685458

What OpenQuestion holds

Textmetadata
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.