Evidence map›Paper›PMID 33211735›Full record

ArticlePloS one2020

Functional role of vitronectin in breast cancer.

Alakesh Bera, Madhan Subramanian, John Karaian, Michael Eklund, Surya Radhakrishnan, Nahbuma Gana, Stephen Rothwell, Harvey Pollard, Hai Hu, Craig D Shriver and 1 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
2.8field-weighted citation impact, top 9% 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

27 citing papers in PubMed, 48 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

11 authors at 3 institutions in 1 country.

Alakesh BeraDepartment of Anatomy, Physiology and Genetics, Uniformed Services University of the Health Sciences (USUHS), Bethesda, Maryland, United States of America.ORCID 0000-0002-2690-8178
Madhan SubramanianDepartment of Anatomy, Physiology and Genetics, Uniformed Services University of the Health Sciences (USUHS), Bethesda, Maryland, United States of America.
John KaraianDepartment of Anatomy, Physiology and Genetics, Uniformed Services University of the Health Sciences (USUHS), Bethesda, Maryland, United States of America.
Michael EklundDepartment of Anatomy, Physiology and Genetics, Uniformed Services University of the Health Sciences (USUHS), Bethesda, Maryland, United States of America.
Surya RadhakrishnanDepartment of Anatomy, Physiology and Genetics, Uniformed Services University of the Health Sciences (USUHS), Bethesda, Maryland, United States of America.
Nahbuma GanaDepartment of Anatomy, Physiology and Genetics, Uniformed Services University of the Health Sciences (USUHS), Bethesda, Maryland, United States of America.
Stephen RothwellDepartment of Anatomy, Physiology and Genetics, Uniformed Services University of the Health Sciences (USUHS), Bethesda, Maryland, United States of America.
Harvey PollardDepartment of Anatomy, Physiology and Genetics, Uniformed Services University of the Health Sciences (USUHS), Bethesda, Maryland, United States of America.
Hai HuChan Soon-Shiong Institute of Molecular Medicine, Windber, Pennsylvania, United States of America.
Craig D ShriverMurtha Cancer Center, Walter Reed National Military Medical Center, Bethesda, Maryland, United States of America.
Meera SrivastavaDepartment of Anatomy, Physiology and Genetics, Uniformed Services University of the Health Sciences (USUHS), Bethesda, Maryland, United States of America.
Uniformed Services University of the Health Sciences · USWalter Reed National Military Medical Center · USWindber Research Institute · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Breast Cancer is the most common form of cancer in women worldwide, impacting nearly 2.1 million women each year. Identification of new biomarkers could be key for early diagnosis and detection. Vitronectin, a glycoprotein that is abundantly found in serum, extracellular matrix, and bone, binds to integrin αvβ3, and promotes cell adhesion and migration. Current studies indicate that patients with amplified vitronectin levels have lower survival rates than patients without amplified vitronectin levels. In this study, we focused on the role of vitronectin in breast cancer survival and its functional role as a non-invasive biomarker for early stage and stage specific breast cancer detection. To confirm that the expression of vitronectin is amplified in breast cancer, a total of 240 serum samples (n = 240), 200 from breast cancer patients and 40 controls were analyzed using the Reverse Phase Protein Array (RPPA) technique. Of the 240 samples, 120 samples were of African American (AA) descent, while the other 120 were of White American (WA) descent. Data indicated that there were some possible racial disparities in vitronectin levels and, differences also seen in the recurrent patient samples. Next, we tried to uncover the underlying mechanism which plays a critical role in vitronectin expression. The cellular data from four different breast cancer cell lines- MCF7, MDA-MB-231, MDA-MB-468, and HCC1599 indicated that the PI3K/AKT axis is modulating the expression of vitronectin. We believe that vitronectin concentration levels are involved and connected to the metastasis of breast cancer in certain patients, specifically based on recurrence or ethnicity, which is detrimental for poor prognosis. Therefore, in this current study we showed that the serum vitronectin levels could be an early marker for the breast cancer survival and we also determine the cellular signaling factors which modulate the expression and concentration of vitronectin.

Indexed as

Gene Expression Regulation, NeoplasticNeoplasm Recurrence, LocalBiomarkers, TumorBreast NeoplasmsCell AdhesionCell Line, TumorCell MovementDisease-Free SurvivalElectrophoresis, CapillaryEthnicityExtracellular MatrixFemaleHumansMCF-7 CellsPhosphatidylinositol 3-KinasesROC CurveBiomarkers, TumorPhosphatidylinositol 3-KinasesVitronectin

Identifiers

PMID33211735
PMCPMC7676670
OpenAlexW3098043307

What OpenQuestion holds

Textmetadata
LicenceCC0
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.