Evidence map›Paper›PMID 35571788›Full record

ArticleACS omega2022

SEMA6D Differentially Regulates Proliferation, Migration, and Invasion of Breast Cell Lines.

Zehra Elif Gunyuz, Ece Sahi-Ilhan, Cansu Kucukkose, Dogac Ipekgil, Gunes Tok, Gulistan Mese, Engin Ozcivici, Ozden Yalcin-Ozuysal

Open access · goldAbstract read
In one paragraph

Article in ACS omega, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.2field-weighted citation impact, top 24% 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

9 citing papers in PubMed, 13 citations in OpenAlex.

  1. Article
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  3. SEMA6A overexpression inhibited tumor growth and metastasis in colorectal cancer.Brazilian journal of medical and biological research = Revista brasileira de pesquisas medicas e biologica · 2025
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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.

Zehra Elif GunyuzDepartment of Molecular Biology and Genetics, Izmir Institute of Technology, 35430 Izmir, Turkey.
Ece Sahi-IlhanDepartment of Molecular Biology and Genetics, Izmir Institute of Technology, 35430 Izmir, Turkey.
Cansu KucukkoseDepartment of Molecular Biology and Genetics, Izmir Institute of Technology, 35430 Izmir, Turkey.
Dogac IpekgilDepartment of Molecular Biology and Genetics, Izmir Institute of Technology, 35430 Izmir, Turkey.
Gunes TokDepartment of Molecular Biology and Genetics, Izmir Institute of Technology, 35430 Izmir, Turkey.
Gulistan MeseDepartment of Molecular Biology and Genetics, Izmir Institute of Technology, 35430 Izmir, Turkey.ORCID https://orcid.org/0000-0003-0458-8684
Engin OzciviciDepartment of Bioengineering, Izmir Institute of Technology, 35430 Izmir, Turkey.
Ozden Yalcin-OzuysalDepartment of Molecular Biology and Genetics, Izmir Institute of Technology, 35430 Izmir, Turkey.ORCID https://orcid.org/0000-0003-0552-368X
Izmir Institute of Technology · TR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Semaphorin 6D (SEMA6D), a member of the class 6 semaphorin family, is a membrane-associated protein that plays a key role in the development of cardiac and neural tissues. A growing body of evidence suggests that SEMA6D is also involved in tumorigenesis. In breast cancer, high SEMA6D levels are correlated with better survival rates. However, very little is known about the functional significance of SEMA6D in breast tumorigenesis. In the present study, we aimed to investigate the effects of SEMA6D expression on the normal breast cell line MCF10A and the breast cancer cell lines MCF7 and MDA MB 231. We demonstrated that SEMA6D expression increases the proliferation of MCF10A cells, whereas the opposite effect was observed in MCF7 cells. SEMA6D expression induced anchorage-independent growth in both cancer cell lines. Furthermore, migration of MCF10A and MCF7 cells and invasion of MDA MB 231 cells were elevated in response to SEMA6D overexpression. Accordingly, the genes related to epithelial-mesenchymal transition (EMT) were altered by SEMA6D expression in MCF10A and MCF7 cell lines. Finally, we provided evidence that SEMA6D levels were associated with the expression of the cell cycle, EMT, and Notch signaling pathway-related genes in breast cancer patients' data. We showed for the first time that SEMA6D overexpression has cell-specific effects on the proliferation, migration, and invasion of normal and cancer breast cell lines, which agrees with the gene expression data of clinical samples. This study lays the groundwork for future research into understanding the functional importance of SEMA6D in breast cancer.

Identifiers

PMID35571788
PMCPMC9097209
OpenAlexW4224997524

What OpenQuestion holds

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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.