Evidence map›Paper›PMID 31273221›Full record

ArticleScientific reports2019

miR-103/107 prolong Wnt/β-catenin signaling and colorectal cancer stemness by targeting Axin2.

Hsin-Yi Chen, Yaw-Dong Lang, Han-Nan Lin, Yun-Ru Liu, Chun-Chieh Liao, André Wendindondé Nana, Yun Yen, Ruey-Hwa Chen

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2019. 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
2.8field-weighted citation impact, top 9% 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, 47 citations in OpenAlex.

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  14. Insulin Resistance and Cancer: In Search for a Causal Link.International journal of molecular sciences · 2021
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  15. Article
  16. MicroRNA-Based Therapeutics for Drug-Resistant Colorectal Cancer.Pharmaceuticals (Basel, Switzerland) · 2021
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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

8 authors at 4 institutions in 1 country.

Hsin-Yi ChenPh.D Program for Cancer Molecular Biology and Drug Discovery, College of Medical Science and Technology, Taipei Medical University, Taipei, Taiwan. hyichen@tmu.edu.tw.
Yaw-Dong LangInstitute of Biomedical Science, Academia Sinica, Taipei, Taiwan.
Han-Nan LinPh.D Program for Cancer Molecular Biology and Drug Discovery, College of Medical Science and Technology, Taipei Medical University, Taipei, Taiwan.
Yun-Ru LiuOffice of Human Research, Taipei Medical University, Taipei, Taiwan.
Chun-Chieh LiaoInstitute of Biological Chemistry, Academia Sinica, Taipei, Taiwan.
André Wendindondé NanaPh.D Program for Cancer Molecular Biology and Drug Discovery, College of Medical Science and Technology, Taipei Medical University, Taipei, Taiwan.
Yun YenPh.D Program for Cancer Molecular Biology and Drug Discovery, College of Medical Science and Technology, Taipei Medical University, Taipei, Taiwan.
Ruey-Hwa ChenInstitute of Biological Chemistry, Academia Sinica, Taipei, Taiwan. rhchen@gate.sinica.edu.tw.
Taipei Medical University · TWInstitute of Biomedical Sciences, Academia Sinica · TWInstitute of Mathematics, Academia Sinica · TWNational Taiwan University · TW

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cancer stemness drives tumor initiation, progression, metastasis, recurrence, and therapy resistance. However, mechanisms that potentiate the acquisition and maintenance of stemness fate of cancer cells remain incompletely understood. Here, we show that miR-103/107 stimulate multiple stem-like features in colorectal cancer, including expression of stem-like markers, appearance of side-population cells, and capabilities in self-renewal, tumor initiation, recurrence, and chemoresistance. Mechanistically, these stemness-promoting functions are mediated by miR-103/107-dependent repression of Axin2, a negative feedback regulator of Wnt/β-catenin signaling. Through inhibiting Axin2, miR-103/107 trigger a prolonged duration of Wnt/β-catenin signaling and a sustained induction of Wnt responsive genes. In colorectal cancer patients, miR-103/107 expression correlates inversely with Axin2 expression and a signature of miR-103/107 high and Axin2 low expression profile correlates with poor prognosis. Together, our study identifies a novel function of miR-103/107 in promoting colorectal cancer stemness by targeting Axin2 and elucidates the clinical relevance and prognostic value of this axis in colorectal cancer.

Indexed as

Gene Expression Regulation, NeoplasticAnimalsApoptosisAxin Proteinbeta CateninBiomarkers, TumorCell ProliferationColorectal NeoplasmsFemaleHumansMiceMice, Inbred BALB CMice, NudeMicroRNAsNeoplastic Stem CellsPrognosisAXIN2 protein, humanAxin Proteinbeta CateninBiomarkers, TumorCTNNB1 protein, humanMicroRNAsMIRN103 microRNA, humanMIRN107 microRNA, humanWnt1 ProteinWNT1 protein, human

Identifiers

PMID31273221
PMCPMC6609830
OpenAlexW2954215258

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.