Evidence map›Paper›PMID 26984280›Full record

ArticleeLife2016

The nucleolar protein NIFK promotes cancer progression via CK1α/β-catenin in metastasis and Ki-67-dependent cell proliferation.

Tsung-Chieh Lin, Chia-Yi Su, Pei-Yu Wu, Tsung-Ching Lai, Wen-An Pan, Yi-Hua Jan, Yu-Chang Chang, Chi-Tai Yeh, Chi-Long Chen, Luo-Ping Ger and 8 more

Open access · goldAbstract read
In one paragraph

Article in eLife, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
2.6field-weighted citation impact, top 10% 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

29 citing papers in PubMed, 45 citations in OpenAlex.

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  7. CTLA-4 silencing could promote anti-tumor effects in hepatocellular.Medical oncology (Northwood, London, England) · 2024
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  11. Screening membraneless organelle participants with machine-learning models that integrate multimodal features.Proceedings of the National Academy of Sciences of the United States of America · 2022
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  12. Article
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  14. The chromatin-binding domain of Ki-67 together with p53 protects human chromosomes from mitotic damage.Proceedings of the National Academy of Sciences of the United States of America · 2021
    Article
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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

18 authors at 9 institutions in 2 countries.

Tsung-Chieh LinGenomics Research Center, Academia Sinica, Taipei, Taiwan.
Chia-Yi SuGenomics Research Center, Academia Sinica, Taipei, Taiwan.
Pei-Yu WuInstitute of Biological Chemistry, Academia Sinica, Taipei, Taiwan.
Tsung-Ching LaiGenomics Research Center, Academia Sinica, Taipei, Taiwan.
Wen-An PanInstitute of Biological Chemistry, Academia Sinica, Taipei, Taiwan.
Yi-Hua JanGenomics Research Center, Academia Sinica, Taipei, Taiwan.
Yu-Chang ChangGenomics Research Center, Academia Sinica, Taipei, Taiwan.
Chi-Tai YehDepartment of Medical Research and Education, Taipei Medical University-Shuang Ho Hospital, New Taipei City, Taiwan.
Chi-Long ChenDepartment of Pathology, Taipei Medical University Hospital, Taipei Medical University, Taipei, Taiwan.
Luo-Ping GerDepartment of Medical Education and Research, Kaohsiung Veterans General, Kaohsiung, Taiwan.
Hong-Tai ChangDepartment of Surgery, Kaohsiung Veterans General, Kaohsiung, Taiwan.
Chih-Jen YangDepartment of Internal Medicine, Kaohsiung Medical University Hospital, Kaohsiung, Taiwan.
Ming-Shyan HuangDepartment of Internal Medicine, Kaohsiung Medical University Hospital, Kaohsiung, Taiwan.ORCID http://orcid.org/0000-0001-8180-2213
Yu-Peng LiuGraduate Institute of Clinical Medicine, Kaohsiung Medical University, Kaohsiung, Taiwan.
Yuan-Feng LinGraduate Institute of Clinical Medicine, College of Medicine, Taipei Medical University, Taipei, Taiwan.
John Y-J ShyyDepartment of Medicine, University of California, San Diego, San Diego, United States.
Ming-Daw TsaiGenomics Research Center, Academia Sinica, Taipei, Taiwan.
Michael HsiaoGenomics Research Center, Academia Sinica, Taipei, Taiwan.ORCID http://orcid.org/0000-0001-8529-9213
Genomics Research Center, Academia Sinica · TWKaohsiung Medical University · TWKaohsiung Veterans General Hospital · TWInstitute of Biological Chemistry, Academia Sinica · TWNational Taiwan University · TWTaipei Medical University · TWTaipei Medical University Hospital · TWTaipei Medical University-Shuang Ho Hospital · TWUniversity of California San Diego · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Nucleolar protein interacting with the FHA domain of pKi-67 (NIFK) is a Ki-67-interacting protein. However, its precise function in cancer remains largely uninvestigated. Here we show the clinical significance and metastatic mechanism of NIFK in lung cancer. NIFK expression is clinically associated with poor prognosis and metastasis. Furthermore, NIFK enhances Ki-67-dependent proliferation, and promotes migration, invasion in vitro and metastasis in vivo via downregulation of casein kinase 1α (CK1α), a suppressor of pro-metastatic TCF4/β-catenin signaling. Inversely, CK1α is upregulated upon NIFK knockdown. The silencing of CK1α expression in NIFK-silenced cells restores TCF4/β-catenin transcriptional activity, cell migration, and metastasis. Furthermore, RUNX1 is identified as a transcription factor of CSNK1A1 (CK1α) that is negatively regulated by NIFK. Our results demonstrate the prognostic value of NIFK, and suggest that NIFK is required for lung cancer progression via the RUNX1-dependent CK1α repression, which activates TCF4/β-catenin signaling in metastasis and the Ki-67-dependent regulation in cell proliferation.

Indexed as

Cell ProliferationNeoplasm MetastasisAnimalsbeta CateninCasein Kinase IIDisease Models, AnimalHumansIntracellular Signaling Peptides and ProteinsKi-67 AntigenKoreaLung NeoplasmsMiceNuclear Proteinsbeta CateninCasein Kinase IICSNK2A1 protein, humanIntracellular Signaling Peptides and ProteinsKi-67 AntigenNIFK protein, humanNuclear Proteinscasein kinase 1 alphacell biologyhumanlung cancermetastasisNIFKrunx1

Identifiers

PMID26984280
PMCPMC4811767
OpenAlexW2306524116

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

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.