Evidence map›Paper›PMID 34344448›Full record

ArticleCell & bioscience2021

EHMT2 promotes the pathogenesis of hepatocellular carcinoma by epigenetically silencing APC expression.

Yuan Guo, Yan-Rong Zhao, Huan Liu, Yang Xin, Jian-Zhi Yu, Yun-Jin Zang, Qing-Guo Xu

Open access · goldAbstract read
In one paragraph

Article in Cell & bioscience, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.5field-weighted citation impact, top 17% 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

13 citing papers in PubMed, 22 citations in OpenAlex.

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  4. EHMT2-mediated transcriptional reprogramming drives neuroendocrine transformation in non-small cell lung cancer.Proceedings of the National Academy of Sciences of the United States of America · 2024
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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

7 authors at 2 institutions in 1 country.

Yuan GuoLiver Disease Center, The Affiliated Hospital of Qingdao University, 59 Haier Blvd, Qingdao, 266000, Shandong, China.
Yan-Rong ZhaoLiver Disease Center, The Affiliated Hospital of Qingdao University, 59 Haier Blvd, Qingdao, 266000, Shandong, China.
Huan LiuOrgan Transplantation Center, The Affiliated Hospital of Qingdao University, 59 Haier Blvd, Qingdao, 266000, Shandong, China.
Yang XinLiver Disease Center, The Affiliated Hospital of Qingdao University, 59 Haier Blvd, Qingdao, 266000, Shandong, China.
Jian-Zhi YuLiver Disease Center, The Affiliated Hospital of Qingdao University, 59 Haier Blvd, Qingdao, 266000, Shandong, China.
Yun-Jin ZangLiver Disease Center, The Affiliated Hospital of Qingdao University, 59 Haier Blvd, Qingdao, 266000, Shandong, China. YunjinZang266@163.com.
Qing-Guo XuOrgan Transplantation Center, The Affiliated Hospital of Qingdao University, 59 Haier Blvd, Qingdao, 266000, Shandong, China. xuqingguo8866@126.com.
Affiliated Hospital of Qingdao University · CNQingdao University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundHepatocellular carcinoma (HCC), the second leading cause of cancer death worldwide, alone accounts for over half (466,100) of new cancer cases and 422,100 deaths based on the average year incidence rates of 2009 to 2011 in China. Due to unclear and complex underlying mechanisms for HCC development, effective therapy for HCC is still unavailable. The Wnt-β-catenin pathway is a critical contributor of HCC pathogenesis: 40-70% of HCCs from patients harbor the nuclear accumulation of β-catenin protein. However, the mechanisms for β-catenin activation are not fully understood.

methodsThe deletion of EHMT2 in Hep3B and Huh1 cells was achieved by transiently transfecting cells with pX459 plasmids, which carry EHMT2 specific small guide RNA (sgRNA) sequences for Cas9 protein. All experiments were performed in triplicate and repeated more than three times.

resultsIn the present study, we observed that EHMT2 (but not EHMT1) mRNA and protein levels were significantly elevated in HCC compared with normal controls. Next, the results of Ki67 staining, as well as MTT, soft-agar and xenograft assays, in wild-type and EHMT2

conclusionAltogether, our observations emphasize that the EHMT2-APC axis is a critical contributor to Wnt-β-catenin pathway activation in HCC, and UNC0642 may be a potential candidate for target drug treatment of HCC.

Indexed as

APCEHMT2Hepatocellular carcinomaUNC0642Wnt–β-catenin pathway

Identifiers

PMID34344448
PMCPMC8335875
OpenAlexW3188108553

What OpenQuestion holds

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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.