Evidence map›Paper›PMID 31966432›Full record

ArticleInternational journal of clinical and experimental pathology2017

DDX51 gene promotes proliferation by activating Wnt/β-catenin signaling in breast cancer.

Weibo Sun, Shundong Cang, Xiaodong Lv, Ping Wang, Quande Lin, Qing Zhang, Zechen Yan, Zhongyang Liu, Yongping Song

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 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.1field-weighted citation impact, top 44% 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

3 citing papers in PubMed, 5 citations in OpenAlex.

  1. Article
  2. Article
  3. RNA Helicases as Shadow Modulators of Cell Cycle Progression.International journal of molecular sciences · 2021
    Review
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

9 authors at 3 institutions in 1 country.

Weibo SunHenan Key Lab of Cancer Stem Cells, Affiliated Cancer Hospital of Zhengzhou University, Zhengzhou University Zhengzhou, Henan, China.
Shundong CangDepartment of Oncology, People's Hospital of Zhengzhou University, The Henan Province People's Hospital Zhengzhou, Henan, China.
Xiaodong LvHenan Key Lab of Cancer Stem Cells, Affiliated Cancer Hospital of Zhengzhou University, Zhengzhou University Zhengzhou, Henan, China.
Ping WangHenan Key Lab of Cancer Stem Cells, Affiliated Cancer Hospital of Zhengzhou University, Zhengzhou University Zhengzhou, Henan, China.
Quande LinHenan Key Lab of Cancer Stem Cells, Affiliated Cancer Hospital of Zhengzhou University, Zhengzhou University Zhengzhou, Henan, China.
Qing ZhangHenan Key Lab of Cancer Stem Cells, Affiliated Cancer Hospital of Zhengzhou University, Zhengzhou University Zhengzhou, Henan, China.
Zechen YanDepartment of Surgery, First Affiliated Hospital of Zhengzhou University Zhengzhou, Henan, China.
Zhongyang LiuDepartment of Surgery, First Affiliated Hospital of Zhengzhou University Zhengzhou, Henan, China.
Yongping SongHenan Key Lab of Cancer Stem Cells, Affiliated Cancer Hospital of Zhengzhou University, Zhengzhou University Zhengzhou, Henan, China.
Henan Cancer Hospital · CNFirst Affiliated Hospital of Zhengzhou University · CNHenan Provincial People's Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Breast cancer was a malignant tumor seriously threatening the life of women in the world. But the prognosis of breast cancer patients was not so satisfactory due to the limited effective therapeutics. The heterogeneity decided that more than one gene or one signaling pathway was responsible for the initiation or progression of breast cancer. DDX51 gene was a member of RNA helicases family in charge of regulation of RNA metabolism. And DDX51 gene was shown to promote proliferation in NSCLC. But we firstly reported the abundant expression of DDX51 gene in both the breast cancer tissues and cell lines in this study. And DDX51 expression was shown to be associated with TNM stage and prognosis in breast cancer patients. When DDX51 was successfully knocked down, either proliferation or DNA synthesis of MCF-7 cells was inhibited. But the ability of migration and invasion of MCF-7 cells was not affected by DDX51 gene. Furthermore, DDX51 knockdown was accompanied by inhibition of Wnt/β-catenin signaling because expression of critical members such as β-catenin, cyclin D1, TCF/LEF, and DKK1 were all affected. Therefore, this study proved that DDX51 gene promoted proliferation in MCF-7 cells by regulating Wnt/β-catenin signaling pathway and showed clinical significance in breast cancer. This study provides us a new promising hope for treatment of patients with breast cancer.

Indexed as

breast cancerDDX51MCF-7Wnt/β-catenin signaling

Identifiers

PMID31966432
PMCPMC6965824
OpenAlexW3026264999

What OpenQuestion holds

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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.