Evidence map›Paper›PMID 36319998›Full record

ReviewMolecular cancer2022

NK cells and solid tumors: therapeutic potential and persisting obstacles.

Le Tong, Carlos Jiménez-Cortegana, Apple H M Tay, Stina Wickström, Lorenzo Galluzzi, Andreas Lundqvist

Open access · goldAbstract readReview
In one paragraph

Review in Molecular cancer, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 116 papers.

0numbers the graph read from it
0cells of the map it votes in
116citing papers in PubMed
12.7field-weighted citation impact, top 1% 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

116 citing papers in PubMed, 163 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. NKG2A inhibition promotes NK cell-CD8Nature communications · 2026
    Article
  13. NK Cell Activation by Platinum Boosts Immunotherapy in HRAdvanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
    Article
  14. Article
  15. Article
  16. Review
  17. Review
  18. Review
  19. Article
  20. Review

56 more citing papers are in PubMed but not listed here.

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

6 authors at 4 institutions in 4 countries.

Le TongDepartment of Oncology-Pathology, Karolinska Institute, Stockholm, Sweden.
Carlos Jiménez-CorteganaDepartment of Radiation Oncology, Weill Cornell Medical College, New York, NY, USA.
Apple H M TayDepartment of Oncology-Pathology, Karolinska Institute, Stockholm, Sweden.
Stina WickströmDepartment of Oncology-Pathology, Karolinska Institute, Stockholm, Sweden.
Lorenzo GalluzziDepartment of Radiation Oncology, Weill Cornell Medical College, New York, NY, USA. deadoc80@gmail.com.
Andreas LundqvistDepartment of Oncology-Pathology, Karolinska Institute, Stockholm, Sweden. andreas.lundqvist@ki.se.
Karolinska Institutet · SECornell University · USNanyang Technological University · SGUniversidad de Sevilla · ES

Funding

Radiation Effect on Immune Cells and the MicrobiomeU54CA274291 · NCI · WEILL MEDICAL COLL OF CORNELL UNIV · PI Joseph O Deasy, Silvia C. Formenti · 2022 to 2026
$9.1M
NCI NIH HHS U54 CA274291
6 · The paper itself

Abstract

Natural killer (NK) cells, which are innate lymphocytes endowed with potent cytotoxic activity, have recently attracted attention as potential anticancer therapeutics. While NK cells mediate encouraging responses in patients with leukemia, the therapeutic effects of NK cell infusion in patients with solid tumors are limited. Preclinical and clinical data suggest that the efficacy of NK cell infusion against solid malignancies is hampered by several factors including inadequate tumor infiltration and persistence/activation in the tumor microenvironment (TME). A number of metabolic features of the TME including hypoxia as well as elevated levels of adenosine, reactive oxygen species, and prostaglandins negatively affect NK cell activity. Moreover, cancer-associated fibroblasts, tumor-associated macrophages, myeloid-derived suppressor cells, and regulatory T cells actively suppress NK cell-dependent anticancer immunity. Here, we review the metabolic and cellular barriers that inhibit NK cells in solid neoplasms as we discuss potential strategies to circumvent such obstacles towards superior therapeutic activity.

Indexed as

Myeloid-Derived Suppressor CellsNeoplasmsHumansKiller Cells, NaturalTumor MicroenvironmentAdoptive cell therapyCAR T cellsCGAS/STING1 signalingImmune checkpoint inhibitorsPD-L1TREG cells

Identifiers

PMID36319998
PMCPMC9623927
OpenAlexW4307757209

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.