Evidence map›Paper›PMID 34596809›Full record

ArticleMolecular biology reports2021

Recombinant water stress protein 1 (Re-WSP1) suppresses colon cancer cell growth through the miR-539/β-catenin signaling pathway.

Songjia Guo, Shuhua Shan, Haili Wu, Huiqiang Hao, Zhuoyu Li

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Article in Molecular biology reports, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

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0cells of the map it votes in
2citing papers in PubMed
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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

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3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Songjia GuoNephrology Department, Shanxi Provincial People's Hospital, 29 Twin Pagoda Temple Street, Taiyuan, China.ORCID http://orcid.org/0000-0001-5754-8251
Shuhua ShanSchool of Life Science, Shanxi University, 92 Wucheng Road, Taiyuan, Shanxi, China.
Haili WuSchool of Life Science, Shanxi University, 92 Wucheng Road, Taiyuan, Shanxi, China.
Huiqiang HaoNephrology Department, Shanxi Provincial People's Hospital, 29 Twin Pagoda Temple Street, Taiyuan, China.ORCID http://orcid.org/0000-0002-5254-3782
Zhuoyu LiSchool of Life Science, Shanxi University, 92 Wucheng Road, Taiyuan, Shanxi, China. lzy@sxu.edu.cn.

Funding

National Natural Science Foundation of China No. 81603020Shanxi Province Science Foundation for Youths 201601D021108
6 · The paper itself

Abstract

backgroundNostoc commune Vauch. is a nitrogen-fixing blue-green algae that expresses a large number of active molecules with medicinal properties. Our previous study found that a water stress protein (WSP1) from N. commune and its recombinant counterpart (Re-WSP1) exhibited significant anti-colon cancer activity both in vitro and in vivo. This study is to investigate the effects of Re-WSP1 on proliferation of colon cancer cells and to elucidate the relevant mechanisms.

methodsReal-time quantitative PCR was used to detect the expression of miR-539 in colon cancer HT-29 and DLD1 cells. Colon cancer cells were transfected with miR-539 mimics and negative controls, and cell proliferation were detected by CCK8 and clonogenic assays. The target gene of miR-539 was predicted, and the dual luciferase reporter gene experiment was used to verify the target gene. After colon cancer cells were transfected with miR-539 mimics or inhibitors, the expression of target gene β-catenin was detected by Western blot. miR-539 inhibitor confirmed cell proliferation.

resultsRe-WSP1 inhibited colon cancer cell growth in a dose-dependent manner. Re-WSP1 inhibited the expression of β-catenin, which was partly reversed by LiCl treatment. Quantitative PCR analysis showed that the expression of miR-539 was significantly upregulated after Re-WSP1 treatment. Moreover, miR-539 negatively regulated the expression of β-catenin by directly binding to the 3'UTR of β-catenin mRNA. The cell growth inhibition and the decrease in β-catenin expression induced by Re-WSP1 were significantly reversed by miR-539 inhibitor.

conclusionRe-WSP1 suppresses colon cancer cell growth via the miR-539/β-catenin axis.

Indexed as

Bacterial Proteinsbeta CateninColonic NeoplasmsHT29 CellsHumansMicroRNAsNeoplasm ProteinsNostoc communeRecombinant ProteinsRNA, NeoplasmSignal TransductionBacterial Proteinsbeta CateninCTNNB1 protein, humanMicroRNAsMIRN539 microRNA, humanNeoplasm ProteinsRecombinant ProteinsRNA, NeoplasmColon cancermicroRNA-539Nostoc commune Vauch.Re-WSP1β-catenin

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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.