Evidence map›Paper›PMID 26124181›Full record

ArticleOncotarget2015

miR-93/miR-106b/miR-375-CIC-CRABP1: a novel regulatory axis in prostate cancer progression.

Nahyun Choi, Jongmin Park, Jeon-Soo Lee, Jeehyun Yoe, Guk Yeol Park, Eunjeong Kim, Hyeongrin Jeon, Yong Mee Cho, Tae-Young Roh, Yoontae Lee

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 57 papers.

0numbers the graph read from it
0cells of the map it votes in
57citing papers in PubMed
5.1field-weighted citation impact, top 4% 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

57 citing papers in PubMed, 90 citations in OpenAlex.

  1. Article
  2. Review
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  6. Article
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  8. TheeLife · 2022
    Article
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  13. Article
  14. Article
  15. Article
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  17. Review
  18. Article
  19. Journal of medical genetics · 2021
    Article
  20. Capicua in Human Cancer.Trends in cancer · 2021
    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

10 authors at 2 institutions in 1 country.

Nahyun ChoiDepartment of Life Sciences, Pohang University of Science and Technology, Pohang, Kyungbuk, Republic of Korea.
Jongmin ParkDepartment of Life Sciences, Pohang University of Science and Technology, Pohang, Kyungbuk, Republic of Korea.
Jeon-Soo LeeDepartment of Life Sciences, Pohang University of Science and Technology, Pohang, Kyungbuk, Republic of Korea.
Jeehyun YoeDepartment of Life Sciences, Pohang University of Science and Technology, Pohang, Kyungbuk, Republic of Korea.
Guk Yeol ParkDepartment of Life Sciences, Pohang University of Science and Technology, Pohang, Kyungbuk, Republic of Korea.
Eunjeong KimDepartment of Life Sciences, Pohang University of Science and Technology, Pohang, Kyungbuk, Republic of Korea.
Hyeongrin JeonDivision of Integrative Bioscience and Biotechnology, Pohang University of Science and Technology, Pohang, Kyungbuk, Republic of Korea.
Yong Mee ChoDepartment of Pathology, University of Ulsan College of Medicine, Asan Medical Center, Seoul, Republic of Korea.
Tae-Young RohDepartment of Life Sciences, Pohang University of Science and Technology, Pohang, Kyungbuk, Republic of Korea.
Yoontae LeeDepartment of Life Sciences, Pohang University of Science and Technology, Pohang, Kyungbuk, Republic of Korea.
Pohang University of Science and Technology · KRUlsan College · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Capicua (CIC) has been implicated in pathogenesis of spinocerebellar ataxia type-1 (SCA1) neurodegenerative disease and some types of cancer; however, the role of CIC in prostate cancer remains unknown. Here we show that CIC suppresses prostate cancer progression. CIC expression was markedly decreased in human prostatic carcinoma. CIC overexpression suppressed prostate cancer cell proliferation, invasion, and migration, whereas CIC RNAi exerted opposite effects. We found that knock-down of CIC derepresses expression of ETV5 and CRABP1 in LNCaP and PC-3 cells, respectively, thereby promoting cell proliferation and invasion. We also discovered that miR-93, miR-106b, and miR-375, which are known to be frequently overexpressed in prostate cancer patients, cooperatively down-regulate CIC levels to promote cancer progression. Altogether, we suggest miR-93/miR-106b/miR-375-CIC-CRABP1 as a novel key regulatory axis in prostate cancer progression.

Indexed as

Gene Expression Regulation, NeoplasticApoptosisCarcinomaCell Line, TumorCell ProliferationDisease ProgressionDNA-Binding ProteinsDown-RegulationGene Expression ProfilingHumansMaleMicroRNAsMicroscopy, FluorescenceNeoplasm InvasivenessProstatic NeoplasmsReceptors, Retinoic AcidCIC protein, humanDNA-Binding ProteinsETV5 protein, humanMicroRNAsMIRN106 microRNA, humanMIRN375 microRNA, humanMIRN93 microRNA, humanReceptors, Retinoic AcidRepressor Proteinsretinoic acid binding protein I, cellularTranscription FactorscapicuaCRABP1ETV5microRNAprostate cancer

Identifiers

PMID26124181
PMCPMC4695135
OpenAlexW1517911595

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.