Evidence map›Paper›PMID 33218358›Full record

ArticleJournal of experimental & clinical cancer research : CR2020

MiR-103a-3p promotes tumour glycolysis in colorectal cancer via hippo/YAP1/HIF1A axis.

Zhenqiang Sun, Qiuge Zhang, Weitang Yuan, Xiaoli Li, Chen Chen, Yaxin Guo, Bo Shao, Qin Dang, Quanbo Zhou, Qisan Wang and 3 more

Open access · goldAbstract read
In one paragraph

Article in Journal of experimental & clinical cancer research : CR, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 72 papers.

0numbers the graph read from it
0cells of the map it votes in
72citing papers in PubMed
5.7field-weighted citation impact, top 3% 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

72 citing papers in PubMed, 135 citations in OpenAlex.

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12 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

13 authors at 3 institutions in 1 country.

Zhenqiang SunDepartment of Colorectal Surgery, The First Affiliated Hospital, Zhengzhou University, Zhengzhou, 450052, Henan, China. zqsun82@csu.edu.cn.
Qiuge ZhangAcademy of Medical Sciences, Zhengzhou University, Zhengzhou, 450052, Henan, China.
Weitang YuanDepartment of Colorectal Surgery, The First Affiliated Hospital, Zhengzhou University, Zhengzhou, 450052, Henan, China.
Xiaoli LiDepartment of Geriatric Medicine, The First Affiliated Hospital, Zhengzhou University, Zhengzhou, 450052, Henan, China.
Chen ChenAcademy of Medical Sciences, Zhengzhou University, Zhengzhou, 450052, Henan, China.
Yaxin GuoSchool of Basic Medical Sciences, Zhengzhou University, Zhengzhou, 450002, Henan, China.
Bo ShaoDepartment of Colorectal Surgery, The First Affiliated Hospital, Zhengzhou University, Zhengzhou, 450052, Henan, China.
Qin DangDepartment of Colorectal Surgery, The First Affiliated Hospital, Zhengzhou University, Zhengzhou, 450052, Henan, China.
Quanbo ZhouDepartment of Colorectal Surgery, The First Affiliated Hospital, Zhengzhou University, Zhengzhou, 450052, Henan, China.
Qisan WangDepartment of Gastrointestinal Surgery, The Affiliated Tumor Hospital, Xinjiang Medical University, Xinjiang, 830000, Urumqi, China.
Guixian WangDepartment of Colorectal Surgery, The First Affiliated Hospital, Zhengzhou University, Zhengzhou, 450052, Henan, China.
Jinbo LiuDepartment of Colorectal Surgery, The First Affiliated Hospital, Zhengzhou University, Zhengzhou, 450052, Henan, China. 1999liujb@163.com.
Quancheng KanDepartment of Pharmacy, The First Affiliated Hospital, Zhengzhou University, Zhengzhou, 450052, Henan, China. kanqc@zzu.edu.cn.
First Affiliated Hospital of Zhengzhou University · CNZhengzhou University · CNXinjiang Medical University · CN

Funding

Key Scientific Research Projects of Institutions of Higher Education in Henan Province 19A310024The China Postdoctoral Science Foundation 2019T120648, 2017M610462The Health Commission Technology Talents Overseas Training Project of Henan Province 2018140The Key Scientific Research Project of Henan Higher Education Institutions 20A310024The Medical Scientific and Technological Research Project of Henan Province 201702027The National Natural Science Foundation of China 81560385, 81972663The National Natural Science Foundation of Henan Province 182300410342
6 · The paper itself

Abstract

backgroundGlycolysis plays an essential role in the growth and metastasis of solid cancer and has received increasing attention in recent years. However, the complex regulatory mechanisms of tumour glycolysis remain elusive. This study aimed to explore the molecular effect and mechanism of the noncoding RNA miR-103a-3p on glycolysis in colorectal cancer (CRC).

methodsWe explored the effects of miR-103a-3p on glycolysis and the biological functions of CRC cells in vitro and in vivo. Furthermore, we investigated whether miR-103a-3p regulates HIF1A expression through the Hippo/YAP1 pathway, and evaluated the role of the miR-103a-3p-LATS2/SAV1-YAP1-HIF1A axis in promoting glycolysis and angiogenesis in CRC cells and contributed to invasion and metastasis of CRC cells.

resultsWe found that miR-103a-3p was highly expressed in CRC tissues and cell lines compared with matched controls and the high expression of miR-103a-3p was associated with poor patient prognosis. Under hypoxic conditions, a high level of miR-103a-3p promoted the proliferation, invasion, migration, angiogenesis and glycolysis of CRC cells. Moreover, miR-103a-3p knockdown inhibited the growth, proliferation, and glycolysis of CRC cells and promoted the Hippo-YAP1 signalling pathway in nude mice in a xenograft model. Here, we demonstrated that miR-103a-3p could directly target LATS2 and SAV1. Subsequently, we verified that TEAD1, a transcriptional coactivator of Yes-associated protein 1 (YAP1), directly bound to the HIF1A promoter region and the YAP1 and TEAD1 proteins co-regulated the expression of HIF1A, thus promoting tumour glycolysis.

conclusionsMiR-103a-3p, which is highly expressed in CRC cells, promotes HIF1A expression by targeting the core molecules LATS2 and SAV1 of the Hippo/YAP1 pathway, contributing to enhanced proliferation, invasion, migration, glycolysis and angiogenesis in CRC. Our study revealed the functional mechanisms of miR-103a-3p/YAP1/HIF1A axis in CRC glycolysis, which would provide potential intervention targets for molecular targeted therapy of CRC.

Indexed as

Adaptor Proteins, Signal TransducingAnimalsCell ProliferationColorectal NeoplasmsDisease Models, AnimalGlycolysisHumansHypoxia-Inducible Factor 1, alpha SubunitMiceMice, NudeMicroRNAsSignal TransductionTranscription FactorsTransfectionYAP-Signaling ProteinsAdaptor Proteins, Signal TransducingHIF1A protein, humanHypoxia-Inducible Factor 1, alpha SubunitMicroRNAsMIRN103A2 microRNA, humanTranscription FactorsYAP1 protein, humanYAP-Signaling ProteinsColorectal cancerGlycolysisHippo pathwayMiR-103a-3p

Identifiers

PMID33218358
PMCPMC7678148
OpenAlexW3100364693

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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.