Evidence map›Paper›PMID 30791364›Full record

ReviewInternational journal of molecular sciences2019

Strengthening the AntiTumor NK Cell Function for the Treatment of Ovarian Cancer.

Marco Greppi, Giovanna Tabellini, Ornella Patrizi, Simona Candiani, Andrea Decensi, Silvia Parolini, Simona Sivori, Silvia Pesce, Laura Paleari, Emanuela Marcenaro

Open access · goldAbstract readReview
In one paragraph

Review in International journal of molecular sciences, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed, 1 pooled it
2.4field-weighted citation impact, top 10% 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

33 citing papers in PubMed, 1 synthesis or guideline pooled it, 55 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Review
  4. PD-1Journal of experimental & clinical cancer research : CR · 2025
    Article
  5. Article
  6. Article
  7. Review
  8. Article
  9. Advances in the treatment of malignant ascites in China.Supportive care in cancer : official journal of the Multinational Association of Supportive Care in Cancer · 2024
    Review
  10. Review
  11. Article
  12. Article
  13. Article
  14. Immune Tumor Microenvironment in Ovarian Cancer Ascites.International journal of molecular sciences · 2022
    Review
  15. Enhanced development of functional human NK cells in NOD-scid-IL2rgFASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2022
    Article
  16. Review
  17. Review
  18. Article
  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

10 authors at 4 institutions in 2 countries.

Marco GreppiDepartment of Experimental Medicine (DIMES) and Centre of Excellence for Biomedical Research (CEBR), University of Genoa, 16132 Genoa, Italy. marcogreppi92@gmail.com.
Giovanna TabelliniDepartment of Molecular and Translational Medicine, University of Brescia, 25123 Brescia, Italy. giovanna.tabellini@unibs.it.
Ornella PatriziDepartment of Molecular and Translational Medicine, University of Brescia, 25123 Brescia, Italy. ornella.patrizi@unibs.it.
Simona CandianiDepartment of Earth Science, Environment and Life (DISTAV), University of Genoa, 16132 Genoa, Italy. candiani@unige.it.ORCID 0000-0002-4453-5475
Andrea DecensiDivision of Medical Oncology, Galliera Hospital, 16126 Genoa, Italy. andrea.decensi@galliera.it.
Silvia ParoliniDepartment of Molecular and Translational Medicine, University of Brescia, 25123 Brescia, Italy. silvia.parolini@unibs.it.
Simona SivoriDepartment of Experimental Medicine (DIMES) and Centre of Excellence for Biomedical Research (CEBR), University of Genoa, 16132 Genoa, Italy. simona.sivori@unige.it.
Silvia PesceDepartment of Experimental Medicine (DIMES), University of Genoa, 16132 Genoa, Italy. silvia.pesce@unige.it.
Laura PaleariA.Li.Sa., Liguria Health Authority, 16121 Genoa, Italy. laura.paleari@regione.liguria.it.
Emanuela MarcenaroDepartment of Experimental Medicine (DIMES) and Centre of Excellence for Biomedical Research (CEBR), University of Genoa, 16132 Genoa, Italy. emanuela.marcenaro@unige.it.ORCID 0000-0003-4103-7566
University of Genoa · ITUniversity of Brescia · ITAgenzia Regionale per la Protezione dell'ambiente ligure · ITQueen Mary University of London · GB

Funding

Associazione Italiana per la Ricerca sul Cancro 20312Associazione Italiana per la Ricerca sul Cancro 21147Associazione Italiana per la Ricerca sul Cancro 21534Roche -
6 · The paper itself

Abstract

The crosstalk between cancer cells and host cells is a crucial prerequisite for tumor growth and progression. The cells from both the innate and adaptive immune systems enter into a perverse relationship with tumor cells to create a tumor-promoting and immunosuppressive tumor microenvironment (TME). Epithelial ovarian cancer (EOC), the most lethal of all gynecological malignancies, is characterized by a unique TME that paves the way to the formation of metastasis and mediates therapy resistance through the deregulation of immune surveillance. A characteristic feature of the ovarian cancer TME is the ascites/peritoneal fluid, a malignancy-associated effusion occurring at more advanced stages, which enables the peritoneal dissemination of tumor cells and the formation of metastasis. The standard therapy for EOC involves a combination of debulking surgery and platinum-based chemotherapy. However, most patients experience disease recurrence. New therapeutic strategies are needed to improve the prognosis of patients with advanced EOC. Harnessing the body's natural immune defenses against cancer in the form of immunotherapy is emerging as an innovative treatment strategy. NK cells have attracted attention as a promising cancer immunotherapeutic target due to their ability to kill malignant cells and avoid healthy cells. Here, we will discuss the recent advances in the clinical application of NK cell immunotherapy in EOC.

Indexed as

ImmunomodulationImmunotherapyBiomarkers, TumorCombined Modality TherapyFemaleHumansKiller Cells, NaturalMolecular Targeted TherapyNeoplasms, Glandular and EpithelialOvarian NeoplasmsTumor EscapeBiomarkers, Tumoractivating receptorsadoptive therapyantitumor activityB7-H6hormone therapyimmune checkpointimmunotherapyNK cellsovarian cancerPD-1

Identifiers

PMID30791364
PMCPMC6412350
OpenAlexW2912951653

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.