Evidence map›Paper›PMID 39349746›Full record

ArticleCommunications biology2024

STAT1 as a tool for non-invasive monitoring of NK cell activation in cancer.

Jin Young Min, Hye Min Kim, Hyunseung Lee, Mi Young Cho, Hye Sun Park, Sang-Yeop Lee, Min Sung Park, Sang Keun Ha, Donghwan Kim, Hye Gwang Jeong and 3 more

Abstract read
In one paragraph

Article in Communications biology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Review
  2. Review
  3. Clinical trial landscape of cellular therapies in bladder cancer.International journal of surgery (London, England) · 2026
    Article
  4. 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

13 authors.

Jin Young Min *Biopharmaceutical Research Center, Korea Basic Science Institute (KBSI), Cheongju, 28119, Republic of Korea.
Hye Min Kim *Biopharmaceutical Research Center, Korea Basic Science Institute (KBSI), Cheongju, 28119, Republic of Korea.ORCID 0009-0009-1762-5238
Hyunseung LeeBiopharmaceutical Research Center, Korea Basic Science Institute (KBSI), Cheongju, 28119, Republic of Korea.
Mi Young ChoBiopharmaceutical Research Center, Korea Basic Science Institute (KBSI), Cheongju, 28119, Republic of Korea.
Hye Sun ParkBiopharmaceutical Research Center, Korea Basic Science Institute (KBSI), Cheongju, 28119, Republic of Korea.ORCID 0000-0002-3275-1437
Sang-Yeop LeeBiopharmaceutical Research Center, Korea Basic Science Institute (KBSI), Cheongju, 28119, Republic of Korea.
Min Sung ParkBiopharmaceutical Research Center, Korea Basic Science Institute (KBSI), Cheongju, 28119, Republic of Korea.
Sang Keun HaKorea University of Science and Technology (UST), Daejeon, 34113, Republic of Korea.
Donghwan KimFood Functionality Research Division, Korea Food Research Institute, Jeollabuk-do, 55365, Republic of Korea.
Hye Gwang JeongCollege of Pharmacy, Chungnam National University, Daejeon, 34134, Republic of Korea.
Tae-Don KimKorea University of Science and Technology (UST), Daejeon, 34113, Republic of Korea.ORCID 0000-0002-5910-4264
Kwan Soo HongBiopharmaceutical Research Center, Korea Basic Science Institute (KBSI), Cheongju, 28119, Republic of Korea. kshong@kbsi.re.kr.
Eun Hee HanBiopharmaceutical Research Center, Korea Basic Science Institute (KBSI), Cheongju, 28119, Republic of Korea. heh4285@kbsi.re.kr.ORCID 0000-0002-0137-0156

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Natural killer (NK) cells play a crucial role in immunotherapy for cancer due to their natural ability to target and destroy cancer cells. However, current methods to visualize NK cells' activity against tumors in live organisms are limited. We introduce an imaging method that non-invasively tracks NK cell activation by cancer cells through the STAT1 protein. To achieve this, we modified NK cells to include a specific genetic sequence that binds to STAT1 when activated. These engineered NK cells (GAS-NK) demonstrate their functionality through various biological tests and analysis. Observations of changes in cancer environments and patient-derived cancer organoid models further confirm the effectiveness of this approach. Our method provides a way to monitor NK cell activity, which could improve the prediction and effectiveness of NK cell-based cancer therapies, contributing to advances in cancer treatment.

Indexed as

Killer Cells, NaturalLymphocyte ActivationNeoplasmsSTAT1 Transcription FactorAnimalsCell Line, TumorHumansTumor MicroenvironmentSTAT1 protein, humanSTAT1 Transcription Factor

Identifiers

PMID39349746
PMCPMC11442705

What OpenQuestion holds

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LicenceCC BY
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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.