Evidence map›Paper›PMID 28748780›Full record

ArticleOncology research2018

miR-133a-3p Targets SUMO-Specific Protease 1 to Inhibit Cell Proliferation and Cell Cycle Progress in Colorectal Cancer.

Guo-Qiang Zhou, Fu Han, Zhi-Liang Shi, Liang Yu, Xue-Feng Li, Cheng Yu, Cheng-Long Shen, Dai-Wei Wan, Xin-Guo Zhu, Rui Li and 1 more

Open access · hybridAbstract read
In one paragraph

Article in Oncology research, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
1.2field-weighted citation impact, top 25% 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

28 citing papers in PubMed, 45 citations in OpenAlex.

  1. Genes · 2026
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  16. Cancer-Associated Dysregulation of Sumo Regulators: Proteases and Ligases.International journal of molecular sciences · 2022
    Review
  17. Article
  18. Review
  19. Article
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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

11 authors at 3 institutions in 1 country.

Guo-Qiang ZhouDepartment of Gastrointestinal Surgery, Changshu No. 2 Hospital, Suzhou, P.R. China.
Fu HanDepartment of Gastrointestinal Surgery, Changshu No. 2 Hospital, Suzhou, P.R. China.
Zhi-Liang ShiDepartment of Gastrointestinal Surgery, Changshu No. 2 Hospital, Suzhou, P.R. China.
Liang YuDepartment of Gastrointestinal Surgery, Changshu No. 2 Hospital, Suzhou, P.R. China.
Xue-Feng LiDepartment of Gastrointestinal Surgery, Changshu No. 2 Hospital, Suzhou, P.R. China.
Cheng YuDepartment of Gastrointestinal Surgery, Changshu No. 2 Hospital, Suzhou, P.R. China.
Cheng-Long ShenDepartment of Gastrointestinal Surgery, Changshu No. 2 Hospital, Suzhou, P.R. China.
Dai-Wei WanDepartment of General Surgery, The First Affiliated Hospital of Soochow University, Suzhou, P.R. China.
Xin-Guo ZhuDepartment of General Surgery, The First Affiliated Hospital of Soochow University, Suzhou, P.R. China.
Rui LiDepartment of Gastroenterology, The First Affiliated Hospital of Soochow University, Suzhou, P.R. China.
Song-Bing HeDepartment of General Surgery, The First Affiliated Hospital of Soochow University, Suzhou, P.R. China.
Changshu No.1 People's Hospital · CNFirst Affiliated Hospital of Soochow University · CNSoochow University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Dysregulation of SUMO-specific protease 1 (SENP1) expression has been reported in several kinds of cancer, including human colorectal and prostate cancers, proposing SENP1 as an oncogene with a critical role in cancer progression. miR-133a-3p has been reported as a tumor suppressor in several malignant neoplasias. However, the precise molecular mechanisms underlying its role in colorectal cancer remain largely unknown. The aim of this work was to investigate the relationship between miR-133a-3p and SENP1 in colorectal cancer cells. We found that miR-133a-3p expression was downregulated in colorectal cancer tissues. In silico analyses indicated that SENP1 is one of the target genes of miR-133a-3p. Overexpression of miR-133a-3p mimics was able to inhibit cell growth with G1 arrest of colorectal cancer cells. Overexpression of miR-133a-3p antisense promoted cell growth of colorectal cancer cells. The luciferase reporter experiments showed that miR-133a-3p regulated the expression of SENP1 by combining with its 3'-UTR and resulted in downregulation of SENP1 and upregulation of CDK inhibitors such as p16, p19, p21, and p27. These results suggest that the miR-133a-3p-SENP1 axis might play a role in cell proliferation and cell cycle regulation of colorectal cancer cells.

Indexed as

Cell CycleCell ProliferationColorectal NeoplasmsCysteine EndopeptidasesGene Expression Regulation, NeoplasticHumansMicroRNAsCysteine EndopeptidasesMicroRNAsMIRN133 microRNA, humanSENP1 protein, human

Identifiers

PMID28748780
PMCPMC7844762
OpenAlexW2742138330

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.