Evidence map›Paper›PMID 42848091›Full record

ArticleMedical oncology (Northwood, London, England)2026

The circMTCL1/miR-145-5p/BMP3 axis suppresses colorectal cancer cell growth by mediating the MAPK signaling pathway.

Liyuan Liu, Dan Jiang, Yongcun Jia, Yuqing Dong, Wei Zhao

Abstract read
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In one paragraph

Article in Medical oncology (Northwood, London, England), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0cells of the map it votes in
0citing papers in PubMed
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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

5 authors.

Liyuan LiuNingxia Institute of Clinical Medicine, People's Hospital of Ningxia Hui Autonomous Region, Ningxia Medical University, NO. 255 Zhengyuan North Street, Yin Chuan, 750002, China. sfy13218@nxmu.edu.cn.ORCID https://orcid.org/0000-0002-3354-2223
Dan JiangGuangdong Provincial Key Laboratory of Medical Immunology and Molecular Diagnostics, The First Dongguan Affiliated Hospital, School of Medical Technology, Guangdong Medical University, Dongguan, 523808, China.
Yongcun JiaNingxia Institute of Clinical Medicine, People's Hospital of Ningxia Hui Autonomous Region, Ningxia Medical University, NO. 255 Zhengyuan North Street, Yin Chuan, 750002, China.
Yuqing DongDepartment of Biochemistry and Molecular Biology, Basic Medical College, Ningxia Medical University, Yinchuan, 750003, China.
Wei ZhaoNingxia Institute of Clinical Medicine, People's Hospital of Ningxia Hui Autonomous Region, Ningxia Medical University, NO. 255 Zhengyuan North Street, Yin Chuan, 750002, China. zhaowei@nxmu.edu.cn.

Funding

Ningxia Natural Science Foundation Project 2023AAC03461the Dongguan Social Development Science and Technology Project 20231800940642the Open Project of the Ningxia Clinical Medical Research Institute 2023KF06the University-Level Scientific Research Project of Ningxia Medical University XM2023074
6 · The paper itself

Abstract

Circular RNAs play key roles in colorectal cancer (CRC). Here, we examine the function and underlying mechanism of circMTCL1 in CRC. The expression of circMTCL1 in CRC tissues and cell lines were detected by quantitative real-time PCR (qRT-PCR). The function of circMTCL1 was elucidated through overexpression and knockdown studies. Furthermore, a combination of Fluorescence in situ hybridization (FISH), nuclear-cytoplasmic fractionation, RNA immunoprecipitation (RIP), qRT-PCR, Western blotting, and dual-luciferase reporter assays was employed to elucidate the tumor-suppressive mechanism of circMTCL1 in CRC. circMTCL1 was significantly downregulated in CRC tissues compared to adjacent normal tissues, showing a 17.08-fold decrease (P < 0.001). It functioned as a competing endogenous RNA (ceRNA) by specifically binding to miR-145-5p, thereby modulating the expression of Bone Morphogenetic Protein 3 (BMP3). Overexpression of circMTCL1 markedly inhibited the proliferation, migration, and invasion of CRC cells, resulting in a 3.76-fold decrease in proliferation (P < 0.001), and 1.58-fold and 2.00-fold decreases in migration and invasion, respectively (P < 0.001). Furthermore, circMTCL1 overexpression upregulated BMP3 expression by 1.60-fold (P < 0.001). Further investigation revealed that circMTCL1 regulates tumor progression by suppressing the activation of the MAPK signaling pathway. circMTCL1 acts as a tumor suppressor in CRC. Its mechanism likely involves sponging miR-145-5p to regulate BMP3 expression and modulating the MAPK signaling pathway. These findings provide a new perspective on the pathogenesis of CRC and identify a potential therapeutic target for clinical intervention.

Indexed as

Bone Morphogenetic Protein 3Colorectal NeoplasmsMAP Kinase Signaling SystemMicroRNAsRNA, CircularCell Line, TumorCell MovementCell ProliferationGene Expression Regulation, NeoplasticHumansRNA, Competitive EndogenousBone Morphogenetic Protein 3MicroRNAsMIRN145 microRNA, humanRNA, CircularRNA, Competitive EndogenousBMP3circMTCL1Colorectal cancermiR-145-5p

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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.