Evidence map›Paper›PMID 36142156›Full record

ArticleInternational journal of molecular sciences2022

SIRT1/FOXO Signaling Pathway in Breast Cancer Progression and Metastasis.

Sayra Dilmac, Nilay Kuscu, Ayse Caner, Sendegul Yildirim, Burcak Yoldas, Ammad Ahmad Farooqi, Gamze Tanriover

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 38 papers.

0numbers the graph read from it
0cells of the map it votes in
38citing papers in PubMed
8.1field-weighted citation impact, top 1% 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

38 citing papers in PubMed, 66 citations in OpenAlex.

  1. SIRT1 in Neurodegenerative Diseases: Molecular Mechanisms, Disease Relevance, and Therapeutic Potential.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2026
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  8. Identification ofFrontiers in pharmacology · 2026
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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 4 institutions in 3 countries.

Sayra DilmacDepartment of Histology and Embryology, School of Medicine, Akdeniz University, 07070 Antalya, Turkey.ORCID 0000-0002-1080-6791
Nilay KuscuDepartment of Histology and Embryology, School of Medicine, Akdeniz University, 07070 Antalya, Turkey.ORCID 0000-0001-7366-6231
Ayse CanerCancer Research Center, Ege University, 35040 Izmir, Turkey.ORCID 0000-0003-3058-9971
Sendegul YildirimDepartment of Histology and Embryology, School of Medicine, Akdeniz University, 07070 Antalya, Turkey.
Burcak YoldasDepartment of Medical Biology and Genetic, School of Medicine, Akdeniz University, 07070 Antalya, Turkey.
Ammad Ahmad FarooqiDepartment of Molecular Oncology, Institute of Biomedical and Genetic Engineering, Islamabad 54000, Pakistan.ORCID 0000-0003-2209-7483
Gamze TanrioverDepartment of Histology and Embryology, School of Medicine, Akdeniz University, 07070 Antalya, Turkey.ORCID 0000-0002-8002-5544
Akdeniz University · TRHouston Methodist · USInstitute of Biomedical and Genetic Engineering · PKThe University of Texas MD Anderson Cancer Center · US

Funding

Akdeniz University TSA-2017-2088
6 · The paper itself

Abstract

Breast cancer is the second most common cancer in women. The roles of the SIRT and FoxO proteins in tumor progression are known, but their roles in metastasis have not yet been clearly elucidated. In our study, we investigated the roles of SIRT and FoxO proteins their downstream pathways, proteins p21 and p53, in tumor progression and metastasis. We evaluated these proteins in vitro using metastatic 4TLM and 67NR cell lines, as well as their expression levels in tumor-bearing mice. In addition, the regulatory role of SIRT and FoxO proteins in different transduction cascades was examined by IPA core analysis, and clinicopathological evidence was investigated in the TCGA database. In primary tumors, the expression levels of SIRT1, p21, p53, E2F1 and FoxO proteins were higher in 67NR groups. In metastatic tissues, the expression levels of SIRT1, E2F1 and FoxO proteins were found to be enhanced, whereas the levels of p53 and p21 expression were noted to be reduced. IPA analysis also provided empirical evidence of the mechanistic involvement of SIRT and FoxO proteins in tumor progression and metastasis. In conclusion, SIRT1 was found to co-operate with FoxO proteins and to play a critical role in metastasis. Additional research is required to determine why overexpression of SIRT1 in metastatic tissues has oncogenic effects.

Indexed as

Breast NeoplasmsSirtuin 1AnimalsCell LineCell Line, TumorFemaleHumansMiceSignal TransductionTumor Suppressor Protein p53SIRT1 protein, humanSirt1 protein, mouseSirtuin 1Tumor Suppressor Protein p53breast cancerFoxOmetastasisprimary tumorSIRT1

Identifiers

PMID36142156
PMCPMC9499652
OpenAlexW4295064601

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.