Evidence map›Paper›PMID 30131941›Full record

ArticleFrontiers in oncology2018

BCMA (TNFRSF17) Induces APRIL and BAFF Mediated Breast Cancer Cell Stemness.

Vasiliki Pelekanou, George Notas, Paraskevi Athanasouli, Konstantinos Alexakis, Fotini Kiagiadaki, Nikolaos Peroulis, Konstantina Kalyvianaki, Errika Kampouri, Hara Polioudaki, Panayiotis Theodoropoulos and 3 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in oncology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
1.7field-weighted citation impact, top 12% 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

31 citing papers in PubMed, 50 citations in OpenAlex.

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  14. Binary MoSMikrochimica acta · 2022
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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

13 authors at 1 institution in 1 country.

Vasiliki PelekanouLaboratory of Experimental Endocrinology, School of Medicine, University of Crete, Heraklion, Greece.
George NotasLaboratory of Experimental Endocrinology, School of Medicine, University of Crete, Heraklion, Greece.
Paraskevi AthanasouliLaboratory of Experimental Endocrinology, School of Medicine, University of Crete, Heraklion, Greece.
Konstantinos AlexakisLaboratory of Experimental Endocrinology, School of Medicine, University of Crete, Heraklion, Greece.
Fotini KiagiadakiLaboratory of Experimental Endocrinology, School of Medicine, University of Crete, Heraklion, Greece.
Nikolaos PeroulisLaboratory of Experimental Endocrinology, School of Medicine, University of Crete, Heraklion, Greece.
Konstantina KalyvianakiLaboratory of Experimental Endocrinology, School of Medicine, University of Crete, Heraklion, Greece.
Errika KampouriLaboratory of Experimental Endocrinology, School of Medicine, University of Crete, Heraklion, Greece.
Hara PolioudakiDepartment of Biochemistry, School of Medicine, University of Crete, Heraklion, Greece.
Panayiotis TheodoropoulosDepartment of Biochemistry, School of Medicine, University of Crete, Heraklion, Greece.
Andreas TsapisLaboratory of Experimental Endocrinology, School of Medicine, University of Crete, Heraklion, Greece.
Elias CastanasLaboratory of Experimental Endocrinology, School of Medicine, University of Crete, Heraklion, Greece.
Marilena KampaLaboratory of Experimental Endocrinology, School of Medicine, University of Crete, Heraklion, Greece.
University of Crete · GR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Recent advances in cancer immunology revealed immune-related properties of cancer cells as novel promising therapeutic targets. The two TNF superfamily members, APRIL (TNFSF13), and BAFF (TNFSF13B), which are type II membrane proteins, released in active forms by proteolytic cleavage and are primarily involved in B-lymphocyte maturation, have also been associated with tumor growth and aggressiveness in several solid tumors, including breast cancer. In the present work we studied the effect of APRIL and BAFF on epithelial to mesenchymal transition, migration, and stemness of breast cancer cells. Our findings show that both molecules increase epithelial to mesenchymal transition and migratory capacity of breast cancer cells, as well as cancer stem cell numbers, by increasing the expression of pluripotency genes such as ALDH1A1, KLF4, and NANOG. These effects are mediated by their common receptor BCMA (TNFRSF17) and the JNK signaling pathway. Interestingly, transcriptional data analysis from breast cancer cells and patients revealed that androgens can increase APRIL transcription and subsequently, in an autocrine/paracrine manner, enhance its pluripotency effect. In conclusion, our data suggest a possible role of APRIL and BAFF in breast cancer disease progression and provide evidence for a new possible mechanism of therapy resistance, that could be particularly relevant in aromatase inhibitors-treated patients, were local androgen is increased.

Indexed as

androgenAPRIL (TNFSF13)aromatase inhibitorsBAFF (TNFSF13B)BCMA (TNFRSF17)cancer stem cellspluripotencytherapy resistance

Identifiers

PMID30131941
PMCPMC6091000
OpenAlexW2885680509

What Socratic 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 Socratic graph.