Evidence map›Paper›PMID 36105584›Full record

ArticleiScience2022

Heterotypic cell-in-cell structures between cancer and NK cells are associated with enhanced anticancer drug resistance.

Yun-Jeong Choe, Jin Young Min, Hyunseong Lee, Sang-Yeop Lee, Joseph Kwon, Hye-Jin Kim, Jangho Lee, Hyun Min Kim, Hye Sun Park, Mi Young Cho and 9 more

Open access · goldAbstract read
In one paragraph

Article in iScience, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.1field-weighted citation impact, top 24% 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

12 citing papers in PubMed, 14 citations in OpenAlex.

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  8. Mitochondrial transfer in tunneling nanotubes-a new target for cancer therapy.Journal of experimental & clinical cancer research : CR · 2024
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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

19 authors at 5 institutions in 1 country.

Yun-Jeong ChoeResearch Center for Bioconvergence Analysis, Korea Basic Science Institute, Cheongju 28119, South Korea.
Jin Young MinResearch Center for Bioconvergence Analysis, Korea Basic Science Institute, Cheongju 28119, South Korea.
Hyunseong LeeResearch Center for Bioconvergence Analysis, Korea Basic Science Institute, Cheongju 28119, South Korea.
Sang-Yeop LeeResearch Center for Bioconvergence Analysis, Korea Basic Science Institute, Cheongju 28119, South Korea.
Joseph KwonResearch Center for Materials Analysis, Korea Basic Science Institute, Daejeon 34133, South Korea.
Hye-Jin KimTomocube, Inc., Daejeon 34051, South Korea.
Jangho LeeResearch Division of Food Functionality, Korea Food Research Institute, Jeollabuk-do 55365, South Korea.
Hyun Min KimResearch Center for Bioconvergence Analysis, Korea Basic Science Institute, Cheongju 28119, South Korea.
Hye Sun ParkResearch Center for Bioconvergence Analysis, Korea Basic Science Institute, Cheongju 28119, South Korea.
Mi Young ChoResearch Center for Bioconvergence Analysis, Korea Basic Science Institute, Cheongju 28119, South Korea.
Ju-Yong HyunResearch Center for Bioconvergence Analysis, Korea Basic Science Institute, Cheongju 28119, South Korea.
Hye Min KimResearch Center for Bioconvergence Analysis, Korea Basic Science Institute, Cheongju 28119, South Korea.
Yong-Ho ChungResearch Center for Bioconvergence Analysis, Korea Basic Science Institute, Cheongju 28119, South Korea.
Sang Keun HaResearch Division of Food Functionality, Korea Food Research Institute, Jeollabuk-do 55365, South Korea.
Hye Gwang JeongDepartment of Toxicology, College of Pharmacy, Chungnam National University, Daejeon 34134, South Korea.
Inpyo ChoiKorea University of Science and Technology (UST), Daejeon 34113, Republic of Korea.
Tae-Don KimKorea University of Science and Technology (UST), Daejeon 34113, Republic of Korea.
Kwan Soo HongResearch Center for Bioconvergence Analysis, Korea Basic Science Institute, Cheongju 28119, South Korea.
Eun Hee HanResearch Center for Bioconvergence Analysis, Korea Basic Science Institute, Cheongju 28119, South Korea.
Korea Basic Science Institute · KRChungnam National University · KRKorea Food Research Institute · KRKorea University of Science and Technology · KRKorea Research Institute of Bioscience and Biotechnology · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The heterotypic CIC structures formed of cancer and immune cells have been observed in tumor tissues. We aimed to assess the feasibility of using heterotypic CICs as a functional biomarker to predict NK susceptibility and drug resistance. The heterotypic CIC-forming cancer cells showed a lower response to NK cytotoxicity and higher proliferative ability than non-CIC cancer cells. After treatment with anticancer drugs, cancer cells that formed heterotypic CICs showed a higher resistance to anticancer drugs than non-CIC cancer cells. We also observed the formation of more CIC structures in cancer cells treated with anticancer drugs than in the non-treated group. Our results confirm the association between heterotypic CIC structures and anticancer drug resistance in CICs formed from NK and cancer cells. These results suggest a mechanism underlying immune evasion in heterotypic CIC cancer cells and provide insights into the anticancer drug resistance of cancer cells.

Indexed as

BiophysicsCancerCell biology

Identifiers

PMID36105584
PMCPMC9464952
OpenAlexW4293563282

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.