Evidence map›Paper›PMID 30291252›Full record

ArticleNature communications2018

Aberrant expression of CITED2 promotes prostate cancer metastasis by activating the nucleolin-AKT pathway.

Seung-Hyun Shin, Ga Young Lee, Mingyu Lee, Jengmin Kang, Hyun-Woo Shin, Yang-Sook Chun, Jong-Wan Park

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 47 papers.

0numbers the graph read from it
0cells of the map it votes in
47citing papers in PubMed
3.1field-weighted citation impact, top 7% 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

47 citing papers in PubMed, 77 citations in OpenAlex.

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  11. Cited2 is a key regulator of placental development and plasticity.BioEssays : news and reviews in molecular, cellular and developmental biology · 2024
    Review
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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

7 authors at 1 institution in 3 countries.

Seung-Hyun ShinDepartment of Biomedical Science, BK21-plus Education Program, Seoul National University College of Medicine, Seoul, Korea.
Ga Young LeeDepartment of Biomedical Science, BK21-plus Education Program, Seoul National University College of Medicine, Seoul, Korea.
Mingyu LeeDepartment of Biomedical Science, BK21-plus Education Program, Seoul National University College of Medicine, Seoul, Korea.
Jengmin KangDepartment of Biomedical Science, BK21-plus Education Program, Seoul National University College of Medicine, Seoul, Korea.
Hyun-Woo ShinDepartment of Biomedical Science, BK21-plus Education Program, Seoul National University College of Medicine, Seoul, Korea.ORCID http://orcid.org/0000-0002-4038-9992
Yang-Sook ChunDepartment of Biomedical Science, BK21-plus Education Program, Seoul National University College of Medicine, Seoul, Korea.
Jong-Wan ParkDepartment of Biomedical Science, BK21-plus Education Program, Seoul National University College of Medicine, Seoul, Korea. parkjw@snu.ac.kr.ORCID http://orcid.org/0000-0003-4676-5191
Seoul National University · KR

Funding

National Research Foundation of Korea (NRF) 2017015015National Research Foundation of Korea (NRF) 2017048432
6 · The paper itself

Abstract

Despite many efforts to develop hormone therapy and chemotherapy, no effective strategy to suppress prostate cancer metastasis has been established because the metastasis is not well understood. We here investigate a role of CBP/p300-interacting transactivator with E/D-rich carboxy-terminal domain-2 (CITED2) in prostate cancer metastasis. CITED2 is highly expressed in metastatic prostate cancer, and its expression is correlated with poor survival. The CITED2 gene is highly activated by ETS-related gene that is overexpressed due to chromosomal translocation. CITED2 acts as a molecular chaperone to guide PRMT5 and p300 to nucleolin, thereby activating nucleolin. Informatics and experimental data suggest that the CITED2-nucleolin axis is involved in prostate cancer metastasis. This axis stimulates cell migration through the epithelial-mesenchymal transition and promotes cancer metastasis in a xenograft mouse model. Our results suggest that CITED2 plays a metastasis-promoting role in prostate cancer and thus could be a target for preventing prostate cancer metastasis.

Indexed as

AcetylationAdenocarcinomaCell MovementEpithelial-Mesenchymal TransitionHEK293 CellsHumansMaleMethylationNeoplasm MetastasisNucleolinp300-CBP Transcription FactorsPC-3 CellsPhosphoproteinsProstatic NeoplasmsProtein-Arginine N-MethyltransferasesProto-Oncogene Proteins c-aktCITED2 protein, humanERG protein, humanNucleolinp300-CBP Transcription FactorsPhosphoproteinsPRMT5 protein, humanProtein-Arginine N-MethyltransferasesProto-Oncogene Proteins c-aktRepressor ProteinsRNA-Binding ProteinsSerine EndopeptidasesTMPRSS2 protein, humanTrans-ActivatorsTranscriptional Regulator ERG

Identifiers

PMID30291252
PMCPMC6173745
OpenAlexW2895446600

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.