Evidence map›Paper›PMID 37545516›Full record

ArticleFrontiers in immunology2023

Intratumoral NKp46

Sylvia M Cruz, Cyrus J Sholevar, Sean J Judge, Morgan A Darrow, Khurshid R Iranpur, Lauren E Farley, Marshall Lammers, Aryana M Razmara, Cordelia Dunai, Alicia A Gingrich and 6 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.8field-weighted citation impact, top 14% 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

15 citing papers in PubMed, 11 citations in OpenAlex.

  1. Article
  2. Mechanistic insights into ferroptosis in thyroid cancer and its therapeutic implications.Apoptosis : an international journal on programmed cell death · 2026
    Review
  3. Genes · 2026
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  4. Article
  5. Review
  6. CD74Journal of translational medicine · 2025
    Article
  7. Review
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. An engineered NKp46 antibody for construction of multi-specific NK cell engagers.Protein engineering, design & selection : PEDS · 2024
    Article
  15. 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

16 authors at 3 institutions in 1 country.

Sylvia M CruzDivision of Surgical Oncology, Department of Surgery, University of California, Davis, Sacramento, CA, United States.
Cyrus J SholevarDivision of Surgical Oncology, Department of Surgery, University of California, Davis, Sacramento, CA, United States.
Sean J JudgeDepartment of Surgery, Memorial Sloan Kettering Cancer Center, New York, NY, United States.
Morgan A DarrowPathology and Laboratory Medicine, University of California, Davis, Sacramento, CA, United States.
Khurshid R IranpurDivision of Surgical Oncology, Department of Surgery, University of California, Davis, Sacramento, CA, United States.
Lauren E FarleyDivision of Surgical Oncology, Department of Surgery, University of California, Davis, Sacramento, CA, United States.
Marshall LammersDivision of Surgical Oncology, Department of Surgery, University of California, Davis, Sacramento, CA, United States.
Aryana M RazmaraDivision of Surgical Oncology, Department of Surgery, University of California, Davis, Sacramento, CA, United States.
Cordelia DunaiDepartment of Dermatology, University of California, Davis, Sacramento, CA, United States.
Alicia A GingrichDepartment of Surgical Oncology, MD Anderson Cancer Center, Houston, TX, United States.
Julia PerskyDivision of Surgical Oncology, Department of Surgery, University of California, Davis, Sacramento, CA, United States.
Hidetoshi MoriCenter for Immunology and Infectious Diseases, University of California, Davis, Sacramento, CA, United States.
Steven W ThorpeOrthopedic Surgery, University of California, Davis, Sacramento, CA, United States.
Arta M MonjazebRadiation Oncology, University of California, Davis, Sacramento, CA, United States.
William J MurphyDepartment of Dermatology, University of California, Davis, Sacramento, CA, United States.
Robert J CanterDivision of Surgical Oncology, Department of Surgery, University of California, Davis, Sacramento, CA, United States.
University of California, Davis · USMemorial Sloan Kettering Cancer Center · USThe University of Texas MD Anderson Cancer Center · US

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI SELWYN M VICKERS · 1985 to 2026
$347.4M
Staff InvestigatorsP30CA093373 · NCI · UNIVERSITY OF CALIFORNIA DAVIS · PI KC KENT LLOYD · 2002 to 2026
$84.9M
UC Davis Comparative Oncology Training ProgramT32CA251007 · NCI · UNIVERSITY OF CALIFORNIA AT DAVIS · PI Robert J. Canter, Xinbin Chen · 2020 to 2026
$1.8M
High-Performance Computing Cluster for Biomedical ResearchS10OD026825 · OD · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI ATHEY, BRIAN DAVID · 2020 to 2020
$600k
UC Davis Shared Astrios Cell SorterS10OD018223 · OD · UNIVERSITY OF CALIFORNIA AT DAVIS · PI SHACKLETT, BARBARA L. · 2015 to 2015
$555k
Gene Expression Analysis of Dog Natural Killer Cells as Immunotherapy TargetR03CA252793 · NCI · UNIVERSITY OF CALIFORNIA AT DAVIS · PI CANTER, ROBERT J. · 2021 to 2022
$157k
Targeting Lung Tissue Resident NK Cells with Inhaled IL-15 and TIGIT Blockade in OsteosarcomaR03CA270854 · NCI · UNIVERSITY OF CALIFORNIA AT DAVIS · PI CANTER, ROBERT J. · 2022 to 2023
$151k
NCI NIH HHS P30 CA008748NCI NIH HHS P30 CA093373NCI NIH HHS R03 CA252793NCI NIH HHS R03 CA270854NCI NIH HHS T32 CA251007NIH HHS S10 OD018223NIH HHS S10 OD026825
6 · The paper itself

Abstract

Introduction: Soft tissue sarcomas (STS) are rare, heterogenous malignancies with an unmet need for novel immunotherapies. Tumor infiltrating lymphocytes (TILs) have been linked with favorable outcomes in STS patients, though the contribution of natural killer (NK) cells and spatial relationships of TILs with MHC-I expressing cells lacks detailed characterization. Experimental design: Using archived and prospectively collected specimens, we evaluated intratumoral NK cells by immunohistochemistry (IHC), flow cytometry, and immunofluorescence (IF). We assessed spatial localization of NK and T cells by multiplex IF, analyzing the effects of MHC-I expression status on NK and T cell clustering. Results: Both intratumoral NKp46 and CD56 Conclusion: Intratumoral NK cells are prognostic in STS and localize closer to MHC-I- cells than T cells. Although both NK and T cells are associated with improved survival in STS, their differential distribution in the TME based on MHC-I expression status may serve as a biomarker for improved immunotherapy treatment selection.

Indexed as

CD8-Positive T-LymphocytesSarcomaSoft Tissue NeoplasmsHumansKiller Cells, NaturalNatural Cytotoxicity Triggering Receptor 1PrognosisNatural Cytotoxicity Triggering Receptor 1NCR1 protein, humanCD56brightCD56dimMHC-Inatural killer cellNKp46soft tissue sarcomasspatial localizationtumor microenvironment

Identifiers

PMID37545516
PMCPMC10401426
OpenAlexW4385050441

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.