Evidence map›Paper›PMID 28176874›Full record

ArticleScientific reports2017

CXCL12/CXCR4 axis induced miR-125b promotes invasion and confers 5-fluorouracil resistance through enhancing autophagy in colorectal cancer.

Xinfeng Yu, Wenna Shi, Yuhang Zhang, Xiaohui Wang, Shiyue Sun, Zhiyu Song, Man Liu, Qiao Zeng, Shuxiang Cui, Xianjun Qu

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 76 papers.

0numbers the graph read from it
0cells of the map it votes in
76citing papers in PubMed
4.5field-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

76 citing papers in PubMed, 123 citations in OpenAlex.

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  5. Nutrients Lowering Obesity-Linked Chemokines Blamable for Metastasis.International journal of molecular sciences · 2025
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16 more citing papers are in PubMed but not listed here.

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.

Xinfeng YuDepartment of Pharmacology, School of Basic Medical Sciences, Capital Medical University, Beijing, China.
Wenna ShiDepartment of Pharmacology, School of Basic Medical Sciences, Capital Medical University, Beijing, China.
Yuhang ZhangDepartment of Pharmacology, School of Basic Medical Sciences, Capital Medical University, Beijing, China.
Xiaohui WangDepartment of General Surgery, Xuan Wu Hospital, Capital Medical University, Beijing, China.
Shiyue SunDepartment of Pharmacology, School of Basic Medical Sciences, Capital Medical University, Beijing, China.
Zhiyu SongDepartment of Pharmacology, School of Basic Medical Sciences, Capital Medical University, Beijing, China.
Man LiuDepartment of Pharmacology, School of Basic Medical Sciences, Capital Medical University, Beijing, China.
Qiao ZengDepartment of Pharmacology, School of Basic Medical Sciences, Capital Medical University, Beijing, China.
Shuxiang CuiBeijing Key Laboratory of Environmental Toxicology, Department of Toxicology and Sanitary Chemistry, School of Public Health, Capital Medical University, Beijing, China.
Xianjun QuDepartment of Pharmacology, School of Basic Medical Sciences, Capital Medical University, Beijing, China.
Capital Medical University · CNXuan Wu Hospital of the Capital Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The activation of CXCL12/CXCR4 axis is associated with potential progression of cancer, such as invasion, metastasis and chemoresistance. However, the underlying mechanisms of CXCL12/CXCR4 axis and cancer progression have been poorly explored. We hypothesized that miRNAs might be critical downstream mediators of CXCL12/CXCR4 axis involved in cancer invasion and chemoresistance in CRC. In human CRC cells, we found that the activation of CXCL12/CXCR4 axis promoted epithelial-mesenchymal transition (EMT) and concurrent upregulation of miR-125b. Overexpression of miR-125b robustly triggered EMT and cancer invasion, which in turn enhanced the expression of CXCR4. Importantly, the reciprocal positive feedback loop between CXCR4 and miR-125b further activated the Wnt/β-catenin signaling by targeting Adenomatous polyposis coli (APC) gene. There was a negative correlation of the expression of miR-125b with APC mRNA in paired human colorectal tissue specimens. Further experiments indicated a role of miR-125b in conferring 5-fluorouracil (5-FU) resistance in CRC probably through increasing autophagy both in vitro and in vivo. MiR-125b functions as an important downstream mediator upon the activation of CXCL12/CXCR4 axis that involved in EMT, invasion and 5-FU resistance of CRC. These findings shed a new insight into the role of miR-125b and provide a potential therapeutic target in CRC.

Indexed as

Signal TransductionAdenomatous Polyposis Coli ProteinAnimalsApoptosisAutophagyBase SequenceCell Line, TumorChemokine CXCL12Colorectal NeoplasmsDrug Resistance, NeoplasmEpithelial-Mesenchymal TransitionFemaleFluorouracilGene Expression Regulation, NeoplasticGenes, Tumor SuppressorHumansAdenomatous Polyposis Coli ProteinChemokine CXCL12CXCL12 protein, humanCXCR4 protein, humanFluorouracilMicroRNAsMIRN125 microRNA, humanReceptors, CXCR4

Identifiers

PMID28176874
PMCPMC5296742
OpenAlexW2586630468

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.