Evidence map›Paper›PMID 39485065›Full record

ArticleCancer biology & medicine2024

Potential treatment approaches for malignant peritoneal mesothelioma: in vivo and in vitro experimental study of natural killer cell immunotherapy.

Heliang Wu, Yi Wang, Yulin Lin, Ru Ma, Xuemei Du, Yandong Su, Rui Yang, Zhiran Yang, Xinli Liang, Yinguang Zhang and 5 more

Abstract read
In one paragraph

Article in Cancer biology & medicine, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
–field-weighted citation impact
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

7 citing papers in PubMed.

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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

15 authors.

Heliang WuDepartment of Peritoneal Cancer Surgery, Beijing Shijitan Hospital, Peking University Ninth School of Clinical Medicine, Beijing 100038, China.
Yi WangDepartment of Hematology, Fifth Medical Center of Chinese PLA General Hospital, Beijing 100071, China.
Yulin LinDepartment of Thoracic Surgery, Zhongshan Hospital, Fudan University (Xiamen Branch), Xiamen 361015, China.
Ru MaDepartment of Peritoneal Cancer Surgery, Beijing Shijitan Hospital, Capital Medical University, Beijing 100038, China.
Xuemei DuDepartment of Pathology, Beijing Friendship Hospital, Capital Medical University, Beijing 100050, China.
Yandong SuDepartment of Peritoneal Cancer Surgery, Beijing Shijitan Hospital, Capital Medical University, Beijing 100038, China.
Rui YangDepartment of Peritoneal Cancer Surgery, Beijing Shijitan Hospital, Capital Medical University, Beijing 100038, China.
Zhiran YangDepartment of Peritoneal Cancer Surgery, Beijing Shijitan Hospital, Capital Medical University, Beijing 100038, China.
Xinli LiangDepartment of Peritoneal Cancer Surgery, Beijing Shijitan Hospital, Capital Medical University, Beijing 100038, China.
Yinguang ZhangDepartment of Thoracic Surgery, Beijing Tiantan Hospital, Capital Medical University, Beijing 100070, China.
Xiaoqing LiangDepartment of Oncology, Beijing Shijitan Hospital, Capital Medical University, Beijing 100038, China.
Zhonghe JiDepartment of Peritoneal Cancer Surgery, Beijing Shijitan Hospital, Capital Medical University, Beijing 100038, China.
Chunning LaiInnovvy Biomedical Technology Co., Ltd., Beijing 100195, China.
Yajing HuangInnovvy Biomedical Technology Co., Ltd., Beijing 100195, China.
Yan LiDepartment of Peritoneal Cancer Surgery, Beijing Shijitan Hospital, Peking University Ninth School of Clinical Medicine, Beijing 100038, China.ORCID 0000-0001-6018-6538

Funding

General Program of National Natural Science Foundation of China 82073376
6 · The paper itself

Abstract

objectiveMalignant peritoneal mesothelioma (MPM) is a rare primary malignant tumor with an extremely poor prognosis that currently lacks effective treatment options. This study investigated the

methodsAn

resultsNK cells effectively killed MPM cells through the release of effector molecules (granzyme B, perforin, interferon-γ, and tumor necrosis factor-α) in a dose- and density-dependent manner. The NK cell killing process potentially involved four dynamic steps: chemotaxis; hitting; adhesion; and penetration. NK cells significantly reduced the tumor burden, diminished ascites production, and extended survival with no significant hematologic toxicity or organ damage in NOG mice.

conclusionsNK cell immunotherapy inhibited proliferation of MPM cells

Indexed as

Killer Cells, NaturalMesotheliomaMesothelioma, MalignantPeritoneal NeoplasmsAnimalsCell Line, TumorCytotoxicity, ImmunologicFemaleHumansImmunotherapyImmunotherapy, AdoptiveLung NeoplasmsMiceXenograft Model Antitumor Assayscell immunotherapyimmunotherapyintraperitoneal injectionMalignant peritoneal mesotheliomanatural killer cells

Identifiers

PMID39485065
PMCPMC11667781

What OpenQuestion holds

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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.