Evidence map›Paper›PMID 32266106›Full record

ArticleAmerican journal of cancer research2020

SMYD2 suppresses APC2 expression to activate the Wnt/β-catenin pathway and promotes epithelial-mesenchymal transition in colorectal cancer.

Fanchao Meng, Xin Liu, Changwei Lin, Lei Xu, Jinjin Liu, Pengbo Zhang, Xiuzhong Zhang, Jun Song, Yichao Yan, Zeqiang Ren and 1 more

Open access · greenAbstract read
In one paragraph

Article in American journal of cancer research, 2020. 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
1.3field-weighted citation impact, top 21% 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, 26 citations in OpenAlex.

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  14. Exploring the Key Signaling Pathways and ncRNAs in Colorectal Cancer.International journal of molecular sciences · 2024
    Review
  15. Article
  16. Wnt/β-catenin-driven EMT regulation in human cancers.Cellular and molecular life sciences : CMLS · 2024
    Review
  17. Article
  18. Review
  19. Review
  20. Article
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 2 institutions in 1 country.

Fanchao MengDepartment of General Surgery, Affiliated Hospital of Xuzhou Medical University Xuzhou 221000, China.
Xin LiuDepartment of Endocrinology, Affiliated Hospital of Xuzhou Medical University Xuzhou 221000, China.
Changwei LinDepartment of General Surgery, Affiliated Hospital of Xuzhou Medical University Xuzhou 221000, China.
Lei XuDepartment of General Surgery, Affiliated Hospital of Xuzhou Medical University Xuzhou 221000, China.
Jinjin LiuDepartment of General Surgery, Affiliated Hospital of Xuzhou Medical University Xuzhou 221000, China.
Pengbo ZhangDepartment of General Surgery, Affiliated Hospital of Xuzhou Medical University Xuzhou 221000, China.
Xiuzhong ZhangDepartment of General Surgery, Affiliated Hospital of Xuzhou Medical University Xuzhou 221000, China.
Jun SongDepartment of General Surgery, Affiliated Hospital of Xuzhou Medical University Xuzhou 221000, China.
Yichao YanDepartment of General Surgery, Affiliated Hospital of Xuzhou Medical University Xuzhou 221000, China.
Zeqiang RenDepartment of General Surgery, Affiliated Hospital of Xuzhou Medical University Xuzhou 221000, China.
Yi ZhangDepartment of General Surgery, Affiliated Hospital of Xuzhou Medical University Xuzhou 221000, China.
Xuzhou Medical College · CNCentral South University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cancer metastasis is a significant challenge in colorectal cancer (CRC) therapy. SET and MYND domain-containing protein 2 (SMYD2) is highly expressed in multiple cancers but is rarely studied in CRC. This study aims to identify whether abnormal expression of SMYD2 is associated with cancer metastasis in CRC. In this study, we demonstrated that SMYD2 not only promoted cell proliferation but also increased the metastatic ability of CRC. The expression of adenomatous polyposis coli 2 (APC2), an inhibitor of the Wnt/β-catenin pathway, was suppressed by SMYD2 overexpression. Overexpression of SMYD2 activated the Wnt/β-catenin pathway and then induced the epithelial-mesenchymal transition (EMT) program in CRC. Mechanistically, low APC2 expression in CRC cells was due to SMYD2-mediated DNA methylation modification. This modification might require synergism with DNMT1. In summary, our study provides new insights into SMYD2-related transcriptional regulation patterns and indicates that SMYD2 could be a potential therapeutic target for CRC patients.

Indexed as

APC2Colorectal cancerDNA methylationEpithelial-mesenchymal transitionSMYD2Wnt/β-catenin pathway

Identifiers

PMID32266106
PMCPMC7136915
OpenAlexW3014930084

What OpenQuestion holds

Textmetadata
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.