Evidence map›Paper›PMID 33322371›Full record

ReviewCancers2020

Prospects for NK Cell Therapy of Sarcoma.

Mieszko Lachota, Marianna Vincenti, Magdalena Winiarska, Kjetil Boye, Radosław Zagożdżon, Karl-Johan Malmberg

Open access · goldAbstract readReview
In one paragraph

Review in Cancers, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
1.1field-weighted citation impact, top 23% 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

19 citing papers in PubMed, 25 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Review
  5. Review
  6. Article
  7. Review
  8. Article
  9. Breast cancer immunotherapy: a comprehensive review.Clinical and experimental medicine · 2023
    Review
  10. Article
  11. Review
  12. Review
  13. Review
  14. Panobinostat enhances NK cell cytotoxicity in soft tissue sarcoma.Clinical and experimental immunology · 2022
    Article
  15. Review
  16. Article
  17. Review
  18. Review
  19. 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

6 authors at 2 institutions in 3 countries.

Mieszko LachotaDepartment of Clinical Immunology, Doctoral School, Medical University of Warsaw, 02-006 Warsaw, Poland.ORCID 0000-0003-2808-8916
Marianna VincentiDepartment of Cancer Immunology, Institute for Cancer Research, Oslo University Hospital, 0310 Oslo, Norway.ORCID 0000-0001-5361-0185
Magdalena WiniarskaDepartment of Immunology, Medical University of Warsaw, 02-097 Warsaw, Poland.
Kjetil BoyeDepartment of Oncology, Oslo University Hospital, 0310 Oslo, Norway.ORCID 0000-0002-5552-6283
Radosław ZagożdżonDepartment of Clinical Immunology, Medical University of Warsaw, 02-006 Warsaw, Poland.ORCID 0000-0002-7957-2372
Karl-Johan MalmbergDepartment of Cancer Immunology, Institute for Cancer Research, Oslo University Hospital, 0310 Oslo, Norway.
Medical University of Warsaw · PLOslo University Hospital · NO

Funding

European Research Council 805038/STIMUNO/ERC-2018-STGMinisterstwo Nauki i Szkolnictwa Wyższego DI2018 020548Narodowe Centrum Nauki 2016/23/B/NZ6/02535
6 · The paper itself

Abstract

Natural killer (NK) cells are innate lymphoid cells with potent antitumor activity. One of the most NK cell cytotoxicity-sensitive tumor types is sarcoma, an aggressive mesenchyme-derived neoplasm. While a combination of radical surgery and radio- and chemotherapy can successfully control local disease, patients with advanced sarcomas remain refractory to current treatment regimens, calling for novel therapeutic strategies. There is accumulating evidence for NK cell-mediated immunosurveillance of sarcoma cells during all stages of the disease, highlighting the potential of using NK cells as a therapeutic tool. However, sarcomas display multiple immunoevasion mechanisms that can suppress NK cell function leading to an uncontrolled tumor outgrowth. Here, we review the current evidence for NK cells' role in immune surveillance of sarcoma during disease initiation, promotion, progression, and metastasis, as well as the molecular mechanisms behind sarcoma-mediated NK cell suppression. Further, we apply this basic understanding of NK-sarcoma crosstalk in order to identify and summarize the most promising candidates for NK cell-based sarcoma immunotherapy.

Indexed as

adoptive cell therapycancercell-mediated cytotoxicitychimeric antigen receptor (CAR)immunotherapyNatural Killer (NK) cellssarcomasolid tumorstumor microenvironment (TME)

Identifiers

PMID33322371
PMCPMC7763692
OpenAlexW3111840869

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.