Evidence map›Paper›PMID 34200450›Full record

ArticleCancers2021

Identification of Nucleolin as a Novel AEG-1-Interacting Protein in Breast Cancer via Interactome Profiling.

Seong-Jae Lee, Kyoung-Min Choi, Geul Bang, Seo-Gyu Park, Eun-Bi Kim, Jin-Woong Choi, Young-Ho Chung, Jinyoung Kim, Seok-Geun Lee, Eunjung Kim and 1 more

Open access · goldAbstract read
In one paragraph

Article in Cancers, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.2field-weighted citation impact, top 22% 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

7 citing papers in PubMed, 14 citations in OpenAlex.

  1. Moesin is an αCellular and molecular life sciences : CMLS · 2026
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  7. Ribosome biogenesis in disease: new players and therapeutic targets.Signal transduction and targeted therapy · 2023
    Review
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

11 authors at 2 institutions in 1 country.

Seong-Jae LeeGraduate School of Analytical Science and Technology (GRAST), Chungnam National University, Daejeon 34134, Korea.
Kyoung-Min ChoiGraduate School of Analytical Science and Technology (GRAST), Chungnam National University, Daejeon 34134, Korea.
Geul BangResearch Center for Bioconvergence Analysis, Korea Basic Science Institute (KBSI), Ochang 28119, Korea.
Seo-Gyu ParkGraduate School of Analytical Science and Technology (GRAST), Chungnam National University, Daejeon 34134, Korea.
Eun-Bi KimGraduate School of Analytical Science and Technology (GRAST), Chungnam National University, Daejeon 34134, Korea.
Jin-Woong ChoiGraduate School of Analytical Science and Technology (GRAST), Chungnam National University, Daejeon 34134, Korea.
Young-Ho ChungResearch Center for Bioconvergence Analysis, Korea Basic Science Institute (KBSI), Ochang 28119, Korea.ORCID 0000-0002-1779-0657
Jinyoung KimResearch Center for Bioconvergence Analysis, Korea Basic Science Institute (KBSI), Ochang 28119, Korea.ORCID 0000-0002-0656-1269
Seok-Geun LeeBionanocomposite Research Center, Department of Science in Korean Medicine, Kyung Hee University, Seoul 02447, Korea.ORCID 0000-0002-0060-5777
Eunjung KimNatural Product Informatics Center, Korea Institute of Science and Technology (KIST), Gangneung 25451, Korea.
Jae-Young KimGraduate School of Analytical Science and Technology (GRAST), Chungnam National University, Daejeon 34134, Korea.
Chungnam National University · KRKorea Basic Science Institute · KR

Funding

Chungnam National University NAKorea Basic Science Institute C170100National Research Foundation of Korea 2019R1A2C1090219National Research Foundation of Korea 2020R1F1A1073114
6 · The paper itself

Abstract

Breast cancer is one of the most common malignant diseases worldwide. Astrocyte elevated gene-1 (AEG-1) is upregulated in breast cancer and regulates breast cancer cell proliferation and invasion. However, the molecular mechanisms by which AEG-1 promotes breast cancer have yet to be fully elucidated. In order to delineate the function of AEG-1 in breast cancer development, we mapped the AEG-1 interactome via affinity purification followed by LC-MS/MS. We identified nucleolin (NCL) as a novel AEG-1 interacting protein, and co-immunoprecipitation experiments validated the interaction between AEG-1 and NCL in breast cancer cells. The silencing of NCL markedly reduced not only migration/invasion, but also the proliferation induced by the ectopic expression of AEG-1. Further, we found that the ectopic expression of AEG-1 induced the tyrosine phosphorylation of c-Met, and NCL knockdown markedly reduced this AEG-1 mediated phosphorylation. Taken together, our report identifies NCL as a novel mediator of the oncogenic function of AEG-1, and suggests that c-Met could be associated with the oncogenic function of the AEG-1-NCL complex in the context of breast cancer.

Indexed as

AEG-1breast cancerLC-MS/MSmetastasisnucleolinprotein-protein interaction

Identifiers

PMID34200450
PMCPMC8201222
OpenAlexW3172847048

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.