Evidence map›Paper›PMID 30678736›Full record

ArticleJournal of experimental & clinical cancer research : CR2019

CXCL12/CXCR4 promotes inflammation-driven colorectal cancer progression through activation of RhoA signaling by sponging miR-133a-3p.

Xinfeng Yu, Dong Wang, Xiaohui Wang, Shiyue Sun, Yuhang Zhang, Shuqing Wang, Rongrong Miao, Xiaoxue Xu, Xianjun Qu

Open access · goldAbstract read
In one paragraph

Article in Journal of experimental & clinical cancer research : CR, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 123 papers.

0numbers the graph read from it
0cells of the map it votes in
123citing papers in PubMed
10.3field-weighted citation impact, top 1% 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

123 citing papers in PubMed, 210 citations in OpenAlex.

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63 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

9 authors at 2 institutions in 1 country.

Xinfeng YuDepartment of Pharmacology, School of Basic Medical Sciences, Capital Medical University, Beijing, China. xinfengyu@hotmail.com.
Dong WangDepartment 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.
Yuhang ZhangDepartment of Pharmacology, School of Basic Medical Sciences, Capital Medical University, Beijing, China.
Shuqing WangDepartment of Pharmacology, School of Basic Medical Sciences, Capital Medical University, Beijing, China.
Rongrong MiaoDepartment of Pharmacology, School of Basic Medical Sciences, Capital Medical University, Beijing, China.
Xiaoxue XuDepartment of Central Laboratory, Capital Medical University, Beijing, China.
Xianjun QuDepartment of Pharmacology, School of Basic Medical Sciences, Capital Medical University, Beijing, China. quxj@ccmu.edu.cn.
Capital Medical University · CNXuan Wu Hospital of the Capital Medical University · CN

Funding

National Natural Science Foundation of China 81201731National Natural Science Foundation of China 91629303Natural Science Foundation of Beijing Municipality 7162024
6 · The paper itself

Abstract

backgroundActivation of CXCL12/CXCR4 axis has been found to be associated with invasion and metastasis in many cancers. However, the underlying mechanism remains elusive. Increasing data highlight that non-coding RNAs are linked to CRC progression.

methodsThe effects of CXCR4 were investigated using villin-CXCR4 transgenic mice model by flow cytometry assay, immunohistochemistry, and Western blot. The mechanism was explored through bioinformatics, luciferase reporter assay and RNA immunoprecipitation assay.

resultsWe found that high CXCR4 expression exacerbated colitis-associated cancer in villin-CXCR4 transgenic mice. CXCR4

conclusionsOur findings revealed the critical role of CXCR4 in promoting progression of inflammatory colorectal cancer through recruiting immunocytes and enhancing cytoskeletal remodeling by lncRNA XIST/ miR-133a-3p/ RhoA signaling. These results provide novel potential therapeutic targets for hindering CXCL12/CXCR4-induced CRC progression.

Indexed as

AnimalsCarcinogenesisCell ProliferationChemokine CXCL12Colorectal NeoplasmsDisease ProgressionEpithelial-Mesenchymal TransitionGene Expression Regulation, NeoplasticHCT116 CellsHumansInflammationMiceMice, KnockoutMicroRNAsNeoplasm InvasivenessReceptors, CXCR4Chemokine CXCL12Cxcl12 protein, mouseCXCR4 protein, mouseMicroRNAsMIRN133 microRNA, humanReceptors, CXCR4rhoA GTP-Binding ProteinRHOA protein, humanRNA, Long NoncodingXIST non-coding RNACACCXCR4lncRNA XISTmiR-133a-3pRhoA

Identifiers

PMID30678736
PMCPMC6346552
OpenAlexW2947386974

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.