Evidence map›Paper›PMID 35228642›Full record

ArticleNPJ precision oncology2022

STAT3 inhibition suppresses adaptive survival of ALK-rearranged lung cancer cells through transcriptional modulation of apoptosis.

Naohiro Yanagimura, Shinji Takeuchi, Koji Fukuda, Sachiko Arai, Azusa Tanimoto, Akihiro Nishiyama, Naohisa Ogo, Hiroyuki Takahashi, Akira Asai, Satoshi Watanabe and 2 more

Open access · goldAbstract read
In one paragraph

Article in NPJ precision oncology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
2.1field-weighted citation impact, top 12% 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

14 citing papers in PubMed, 14 citations in OpenAlex.

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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

12 authors at 3 institutions in 1 country.

Naohiro YanagimuraDivision of Medical Oncology Cancer Research Institute, Kanazawa University, Kanazawa, Japan.
Shinji TakeuchiDivision of Medical Oncology Cancer Research Institute, Kanazawa University, Kanazawa, Japan. takeuchi@staff.kanazawa-u.ac.jp.ORCID http://orcid.org/0000-0002-3779-1454
Koji FukudaDivision of Medical Oncology Cancer Research Institute, Kanazawa University, Kanazawa, Japan.ORCID http://orcid.org/0000-0001-8544-6244
Sachiko AraiDivision of Medical Oncology Cancer Research Institute, Kanazawa University, Kanazawa, Japan.
Azusa TanimotoDivision of Medical Oncology Cancer Research Institute, Kanazawa University, Kanazawa, Japan.
Akihiro NishiyamaDivision of Medical Oncology Cancer Research Institute, Kanazawa University, Kanazawa, Japan.
Naohisa OgoCenter for Drug Discovery, Graduate School of Pharmaceutical Sciences, University of Shizuoka, Shizuoka, Japan.
Hiroyuki TakahashiCenter for Drug Discovery, Graduate School of Pharmaceutical Sciences, University of Shizuoka, Shizuoka, Japan.
Akira AsaiCenter for Drug Discovery, Graduate School of Pharmaceutical Sciences, University of Shizuoka, Shizuoka, Japan.
Satoshi WatanabeDepartment of Respiratory Medicine and Infectious Diseases, Niigata University Graduate School of Medical and Dental Sciences, Niigata, Japan.
Toshiaki KikuchiDepartment of Respiratory Medicine and Infectious Diseases, Niigata University Graduate School of Medical and Dental Sciences, Niigata, Japan.
Seiji YanoDivision of Medical Oncology Cancer Research Institute, Kanazawa University, Kanazawa, Japan. syano@staff.kanazawa-u.ac.jp.
Kanazawa University · JPUniversity of Shizuoka · JPNiigata University · JP

Funding

MEXT | Japan Society for the Promotion of Science (JSPS) 19H03665MEXT | Japan Society for the Promotion of Science (JSPS) 19K16738MEXT | Japan Society for the Promotion of Science (JSPS) 20K08516
6 · The paper itself

Abstract

Patients with advanced anaplastic lymphoma kinase (ALK)-rearranged non-small cell lung cancer who are prescribed ALK-tyrosine kinase inhibitors (ALK-TKIs) rarely have complete responses, with residual tumors relapsing as heterogeneous resistant phenotypes. Herein, we investigated new therapeutic strategies to reduce and eliminate residual tumors in the early treatment phase. Functional genomic screening using small guide RNA libraries showed that treatment-induced adaptive survival of ALK-rearranged lung cancer cells was predominantly dependent on STAT3 activity upon ALK inhibition. STAT3 inhibition effectively suppressed the adaptive survival of ALK-rearranged lung cancer cells by enhancing ALK inhibition-induced apoptosis. The combined effects were characterized by treatment-induced STAT3 dependence and transcriptional regulation of anti-apoptotic factor BCL-X

Identifiers

PMID35228642
PMCPMC8885877
OpenAlexW4214838716

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.