Evidence map›Paper›PMID 28107479›Full record

ArticlePloS one2017

Apoptosis Induction and Gene Expression Profile Alterations of Cutaneous T-Cell Lymphoma Cells following Their Exposure to Bortezomib and Methotrexate.

Vassiliki Mpakou, Evangelia Papadavid, Frieda Kontsioti, Eugene Konsta, Miriam Vikentiou, Aris Spathis, Sotiris Papageorgiou, Diamantina Vasilatou, Konstantinos Gkontopoulos, Efthimia Mpazani and 4 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
1.1field-weighted citation impact, top 22% 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

4 citing papers in PubMed, 5 citations in OpenAlex.

  1. Article
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  4. Review
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

14 authors at 2 institutions in 1 country.

Vassiliki MpakouSecond Dept. of Internal Medicine and Research Institute, Attikon University General Hospital, Rimini 1, Haidari, Athens, Greece.
Evangelia PapadavidSecond Department of Dermatology, Attikon University General Hospital, Rimini 1, Haidari, Athens, Greece.
Frieda KontsiotiSecond Dept. of Internal Medicine and Research Institute, Attikon University General Hospital, Rimini 1, Haidari, Athens, Greece.
Eugene KonstaSecond Dept. of Internal Medicine and Research Institute, Attikon University General Hospital, Rimini 1, Haidari, Athens, Greece.
Miriam VikentiouSecond Dept. of Internal Medicine and Research Institute, Attikon University General Hospital, Rimini 1, Haidari, Athens, Greece.
Aris SpathisDepartment of Cytopathology, Attikon University General Hospital, Athens, Greece.
Sotiris PapageorgiouSecond Dept. of Internal Medicine and Research Institute, Attikon University General Hospital, Rimini 1, Haidari, Athens, Greece.
Diamantina VasilatouSecond Dept. of Internal Medicine and Research Institute, Attikon University General Hospital, Rimini 1, Haidari, Athens, Greece.
Konstantinos GkontopoulosSecond Dept. of Internal Medicine and Research Institute, Attikon University General Hospital, Rimini 1, Haidari, Athens, Greece.
Efthimia MpazaniSecond Dept. of Internal Medicine and Research Institute, Attikon University General Hospital, Rimini 1, Haidari, Athens, Greece.
Petros KarakitsosDepartment of Cytopathology, Attikon University General Hospital, Athens, Greece.
Dimitrios RigopoulosSecond Department of Dermatology, Attikon University General Hospital, Rimini 1, Haidari, Athens, Greece.
George DimitriadisSecond Dept. of Internal Medicine and Research Institute, Attikon University General Hospital, Rimini 1, Haidari, Athens, Greece.
Vasiliki PappaSecond Dept. of Internal Medicine and Research Institute, Attikon University General Hospital, Rimini 1, Haidari, Athens, Greece.ORCID http://orcid.org/0000-0003-0421-9424
University General Hospital Attikon · GRAndreas Sygros Hospital · GR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Mycosis fungoides (MF) and its leukemic variant Sézary syndrome (SS) comprise the majority of CTCL, a heterogenous group of non-Hodgkins lymphomas involving the skin. The CTCL's resistance to chemotherapy and the lack of full understanding of their pathogenesis request further investigation. With the view of a more targeted therapy, we evaluated in vitro the effectiveness of bortezomib and methotrexate, as well as their combination in CTCL cell lines, regarding apoptosis induction. Our data are of clinical value and indicate that the bortezomib/methotrexate combinational therapy has an inferior impact on the apoptosis of CTCL compared to monotherapy, with bortezomib presenting as the most efficient treatment option for SS and methotrexate for MF. Using PCR arrays technology, we also investigated the alterations in the expression profile of genes related to DNA repair pathways in CTCL cell lines after treatment with bortezomib or methotrexate. We found that both agents, but mostly bortezomib, significantly deregulate a large number of genes in SS and MF cell lines, suggesting another pathway through which these agents could induce apoptosis in CTCL. Finally, we show that SS and MF respond differently to treatment, verifying their distinct nature and further emphasizing the need for discrete treatment approaches.

Indexed as

Gene Expression ProfilingAntineoplastic AgentsApoptosisBortezomibCell Line, TumorDNA RepairFlow CytometryHumansLymphoma, T-Cell, CutaneousMethotrexatePolymerase Chain ReactionSignal TransductionAntineoplastic AgentsBortezomibMethotrexate

Identifiers

PMID28107479
PMCPMC5249051
OpenAlexW2573860814

What OpenQuestion holds

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LicenceCC BY
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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.