Evidence map›Paper›PMID 31799197›Full record

ArticleFrontiers in oncology2019

FAM53A Affects Breast Cancer Cell Proliferation, Migration, and Invasion in a p53-Dependent Manner.

Jie Zhang, Mingfang Sun, Miaomiao Hao, Kexin Diao, Jian Wang, Shiping Li, Qixue Cao, Xiaoyi Mi

Open access · goldAbstract read
In one paragraph

Article in Frontiers in oncology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
0.5field-weighted citation impact, top 30% 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

10 citing papers in PubMed, 15 citations in OpenAlex.

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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

8 authors at 1 institution in 1 country.

Jie ZhangDepartment of Pathology, College of Basic Medical Sciences, First Affiliated Hospital, China Medical University, Shenyang, China.
Mingfang SunDepartment of Pathology, College of Basic Medical Sciences, First Affiliated Hospital, China Medical University, Shenyang, China.
Miaomiao HaoDepartment of Pathology, College of Basic Medical Sciences, First Affiliated Hospital, China Medical University, Shenyang, China.
Kexin DiaoDepartment of Pathology, College of Basic Medical Sciences, First Affiliated Hospital, China Medical University, Shenyang, China.
Jian WangDepartment of Pathology, College of Basic Medical Sciences, First Affiliated Hospital, China Medical University, Shenyang, China.
Shiping LiDepartment of Pathology, College of Basic Medical Sciences, First Affiliated Hospital, China Medical University, Shenyang, China.
Qixue CaoDepartment of Pathology, College of Basic Medical Sciences, First Affiliated Hospital, China Medical University, Shenyang, China.
Xiaoyi MiDepartment of Pathology, College of Basic Medical Sciences, First Affiliated Hospital, China Medical University, Shenyang, China.
China Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Family with sequence similarity 53-member A (FAM53A) is an uncharacterized protein with a suspected but unclear role in tumorigenesis. In this study, we examined its role in breast cancer. Immunohistochemical staining of specimens from 199 cases of breast cancer demonstrated that FAM53A levels were negatively correlated with p53 status. In the p53 wild-type breast cancer cell line MCF-7, FAM53A overexpression inhibited cell migration, invasion, and proliferation, downregulated the expression of Snail, cyclin D1, RhoA, RhoC, and MMP9, and decreased mitogen-activated protein kinase kinase (MEK) and extracellular-signal regulated kinase (ERK) phosphorylation. Concurrently, it upregulated E-cadherin and p21 expression levels. Interestingly, opposite trends were observed in the p53-null breast cancer cell line MDA-MB-231. The MEK inhibitor PD98059 reduced the biological effects of FAM53A knockdown in MCF-7 cells and FAM53A overexpression in MDA-MB-231 cells, suggesting that FAM53A affects breast cancer through the MEK-ERK pathway. Silencing

Indexed as

breast cancercell migrationepithelial-mesenchymal transition (EMT)extracellular-signal-regulated kinase (ERK)invasionmetastasisp53

Identifiers

PMID31799197
PMCPMC6874147
OpenAlexW2988927692

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.