Evidence map›Paper›PMID 37370835›Full record

ArticleCancers2023

Enhancement of the Anticancer Ability of Natural Killer Cells through Allogeneic Mitochondrial Transfer.

Seong-Hoon Kim, Mi-Jin Kim, Mina Lim, Jihye Kim, Hyunmin Kim, Chang-Koo Yun, Yun-Joo Yoo, Youngjun Lee, Kyunghoon Min, Yong-Soo Choi

Abstract read
In one paragraph

Article in Cancers, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing 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

18 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

10 authors.

Seong-Hoon KimDepartment of Biotechnology, CHA University, Seongnam 13488, Republic of Korea.ORCID 0009-0002-9556-6076
Mi-Jin KimDepartment of Biotechnology, CHA University, Seongnam 13488, Republic of Korea.ORCID 0000-0002-0594-5703
Mina LimDepartment of Biotechnology, CHA University, Seongnam 13488, Republic of Korea.
Jihye KimDepartment of Quantitative Health Sciences, Cleveland Clinic Lerner Research Institute, Cleveland, OH 44195, USA.
Hyunmin KimDepartment of Genetics and Genome Sciences, Case Western Reserve University School of Medicine, Cleveland, OH 44106, USA.
Chang-Koo YunDepartment of Biotechnology, CHA University, Seongnam 13488, Republic of Korea.
Yun-Joo YooDepartment of Biotechnology, CHA University, Seongnam 13488, Republic of Korea.
Youngjun LeeResearch & Development Division, Humancellbio Co., Ltd., Suwon 16227, Republic of Korea.
Kyunghoon MinDepartment of Rehabilitation Medicine, CHA Bundang Medical Center, CHA University School of Medicine, Seongnam 13496, Republic of Korea.ORCID 0000-0003-3357-9795
Yong-Soo ChoiDepartment of Biotechnology, CHA University, Seongnam 13488, Republic of Korea.ORCID 0000-0001-8445-8067

Funding

National Research Foundation of Korea (NRF) by the Korean government (MSIT) 2022R1A2C100716011
6 · The paper itself

Abstract

An in vitro culture period of at least 2 weeks is required to produce sufficient natural killer (NK) cells for immunotherapy, which are the key effectors in hematological malignancy treatment. Mitochondrial damage and fragmentation reduce the NK cell immune surveillance capacity. Thus, we hypothesized that the transfer of healthy mitochondria to NK cells could enhance their anticancer effects. Allogeneic healthy mitochondria isolated from WRL-68 cells were transferred to NK cells. We evaluated NK cells' proliferative capacity, cell cycle, and cytotoxic capacity against various cancer cell types by analyzing specific lysis and the cytotoxic granules released. The relationship between the transferred allogenic mitochondrial residues and NK cell function was determined. After mitochondrial transfer, the NK cell proliferation rate was 1.2-fold higher than that of control cells. The mitochondria-treated NK cells secreted a 2.7-, 4.1-, and 5-fold higher amount of granzyme B, perforin, and IFN-γ, respectively, when co-cultured with K562 cells. The specific lysis of various solid cancer cells increased 1.3-1.6-fold. However, once allogeneic mitochondria were eliminated, the NK cell activity returned to the pre-mitochondrial transfer level. Mitochondria-enriched NK cells have the potential to be used as a novel solid cancer treatment agent, without the need for in vitro cytokine-induced culture.

Indexed as

anticancer immunotherapyimmune cell therapymitochondriamitochondrial transfernatural killer cells

Identifiers

PMID37370835
PMCPMC10296914

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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.