Evidence map›Paper›PMID 31966514›Full record

ArticleInternational journal of clinical and experimental pathology2017

Dact3 inhibits the malignant phenotype of non-small cell lung cancer through downregulation of c-Myb.

Huanyu Zhao, Lianhe Yang, Yang Han, Hongqiang Li, Zihan Ling, Yan Wang, Enhua Wang, Guangping Wu

Open access · greenAbstract read
In one paragraph

Article in International journal of clinical and experimental pathology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.1field-weighted citation impact, top 46% 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

7 citing papers in PubMed, 12 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
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  5. Article
  6. The Role of DACT Family Members in Tumorigenesis and Tumor Progression.International journal of biological sciences · 2022
    Review
  7. 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

8 authors at 2 institutions in 1 country.

Huanyu ZhaoDepartment of Pathology, The First Affiliated Hospital and College of Basic Medical Sciences, China Medical University Shenyang, Liaoning, China.
Lianhe YangDepartment of Pathology, The First Affiliated Hospital and College of Basic Medical Sciences, China Medical University Shenyang, Liaoning, China.
Yang HanDepartment of Pathology, The First Affiliated Hospital and College of Basic Medical Sciences, China Medical University Shenyang, Liaoning, China.
Hongqiang LiDepartment of Pathology, The First Affiliated Hospital and College of Basic Medical Sciences, China Medical University Shenyang, Liaoning, China.
Zihan LingLiaoning Province Shiyan High School Shenyang, Liaoning, China.
Yan WangDepartment of Pathology, The First Affiliated Hospital and College of Basic Medical Sciences, China Medical University Shenyang, Liaoning, China.
Enhua WangDepartment of Pathology, The First Affiliated Hospital and College of Basic Medical Sciences, China Medical University Shenyang, Liaoning, China.
Guangping WuDepartment of Pathology, The First Affiliated Hospital and College of Basic Medical Sciences, China Medical University Shenyang, Liaoning, China.
First Hospital of China Medical University · CNLiaoning University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Dact3 is a negative regulator of Wnt/β-catenin signaling. c-Myb promotes tumor cell invasion through Wnt/β-catenin pathway. However, the detailed mechanism by which Dact3 and c-Myb modulate the progression of non-small cell lung cancer (NSCLC) remains unclear. In this study, the expressions of Dact3 and c-Myb in 254 surgically resected NSCLC samples were detected by immunohistochemistry. We transfected Dact3 cDNA to A549 and H157 cells or siRNA-Dact3 to SPC cells and examined above effects on the activity of Wnt/β-catenin signaling by Western blot and luciferase activity assay, in addition to cell biological behavior by Transwell and MTT assay. Dact3 expression was reduced in NSCLC tissue. Reduced Dact3 expression was correlated with lymph node metastasis and poor prognosis of NSCLC (P<0.05). In addition, Dact3 expression was negatively correlated with the c-Myb expression (R = -0.626, P<0.05). Dact3 transfection resulted in c-Myb reduced expression in NSCLC cells, as well as decreased activity of Wnt/β-catenin signaling and reduced cell invasive and proliferative capacity. siRNA-Dact3 transfection had the opposite effect. Our results indicate that Dact3 may inhibit the malignant phenotype of NSCLC through downregulation of c-Myb.

Indexed as

c-Mybc-MycDact3NSCLCβ-catenin

Identifiers

PMID31966514
PMCPMC6966047
OpenAlexW3010981228

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.