Evidence map›Paper›PMID 30559932›Full record

ArticleOncotarget2018

Intratumoral CD56

Neelam Mukherjee, Niannian Ji, Vincent Hurez, Tyler J Curiel, Maureen O Montgomery, Andrew J Braun, Marlo Nicolas, Marcela Aguilera, Dharam Kaushik, Qianqian Liu and 3 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 45 papers.

0numbers the graph read from it
0cells of the map it votes in
45citing papers in PubMed
2.2field-weighted citation impact, top 12% 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

45 citing papers in PubMed, 63 citations in OpenAlex.

  1. Trial
  2. Article
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  6. Article
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  8. Review
  9. Article
  10. Article
  11. Review
  12. Article
  13. Article
  14. Transcriptional signature of CD56Frontiers in immunology · 2024
    Article
  15. Review
  16. Article
  17. KLRF1, a novel marker of CD56Cancer medicine · 2023
    Article
  18. Article
  19. Article
  20. Article
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

13 authors at 2 institutions in 1 country.

Neelam MukherjeeDepartment of Urology, University of Texas Health San Antonio (UTHSA), San Antonio, United States.
Niannian JiDepartment of Urology, University of Texas Health San Antonio (UTHSA), San Antonio, United States.
Vincent HurezDepartment of Medicine, University of Texas Health San Antonio (UTHSA), San Antonio, United States.
Tyler J CurielDepartment of Medicine, University of Texas Health San Antonio (UTHSA), San Antonio, United States.
Maureen O MontgomeryDepartment of Urology, University of Texas Health San Antonio (UTHSA), San Antonio, United States.
Andrew J BraunDepartment of Urology, University of Texas Health San Antonio (UTHSA), San Antonio, United States.
Marlo NicolasDepartment of Pathology, University of Texas Health San Antonio (UTHSA), San Antonio, United States.
Marcela AguileraDepartment of Computer Science, University of Texas San Antonio (UTSA), San Antonio, United States.
Dharam KaushikDepartment of Urology, University of Texas Health San Antonio (UTHSA), San Antonio, United States.
Qianqian LiuDepartment of Epidemiology & Biostatistics, University of Texas Health San Antonio (UTHSA), San Antonio, United States.
Jianhua RuanDepartment of Computer Science, University of Texas San Antonio (UTSA), San Antonio, United States.
Kerri A KendrickDepartment of Urology, University of Texas Health San Antonio (UTHSA), San Antonio, United States.
Robert S SvatekDepartment of Urology, University of Texas Health San Antonio (UTHSA), San Antonio, United States.
The University of Texas Health Science Center at San Antonio · USThe University of Texas at San Antonio · US

Funding

Improving immunotherapy in bladder cancer by targeting immune dysfunctionK23CA178204 · NCI · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI SVATEK, ROBERT SCOTT · 2014 to 2017
$674k
NCI NIH HHS K23 CA178204
6 · The paper itself

Abstract

backgroundNatural killer (NK) cells are effective at killing tumors in a non-MHC restricted manner and are emerging targets for cancer therapy but their importance in bladder cancer (BC) is poorly defined. NK cells are commonly subdivided into populations based on relative surface expression of CD56. Two major subsets are CD56

methodsThe prevalence of intratumoral lymphocytes was examined via flow cytometric analysis of bladder tissue from a local cohort of patients with non-invasive and invasive BC (n=28). The association of NK cell subsets with cancer-specific survival (CSS) and overall survival (OS) was examined in 50 patients with BC using Cox regression. Fluorescence-activated cell sorting (FACS) of intratumoral lymphocytes isolated CD56 NK cell subsets were used for examination of function, including cytokine production and

resultsNK cells predominated among bladder intratumoral lymphocytes. Intratumoral CD56

conclusionsNK cells are frequent among intratumoral lymphocytes in BC. Bladder intratumoral CD56

Indexed as

bladder cancerCD56NK cellssurvivaltumor-infiltrating lymphocytes

Identifiers

PMID30559932
PMCPMC6284861
OpenAlexW2901261720

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.