Evidence map›Paper›PMID 34072003›Full record

ArticleCancers2021

Lensoside Aβ as an Adjuvant to the Anti-Glioma Potential of Sorafenib.

Aleksandra Maciejczyk, Justyna Kapral-Piotrowska, Joanna Sumorek-Wiadro, Adrian Zając, Ewa Grela, Rafał Luchowski, Wiesław I Gruszecki, Marta Kinga Lemieszek, Iwona Wertel, Łukasz Pecio and 7 more

Open access · goldAbstract read
In one paragraph

Article in Cancers, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.2field-weighted citation impact, top 48% 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

2 citing papers in PubMed, 5 citations in OpenAlex.

  1. Article
  2. CaInternational journal of molecular sciences · 2023
    Article
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

17 authors at 4 institutions in 1 country.

Aleksandra MaciejczykDepartment of Functional Anatomy and Cytobiology, Institute of Biological Sciences, Maria Curie-Sklodowska University, Akademicka 19, 20-033 Lublin, Poland.
Justyna Kapral-PiotrowskaDepartment of Functional Anatomy and Cytobiology, Institute of Biological Sciences, Maria Curie-Sklodowska University, Akademicka 19, 20-033 Lublin, Poland.ORCID 0000-0001-9961-574X
Joanna Sumorek-WiadroDepartment of Functional Anatomy and Cytobiology, Institute of Biological Sciences, Maria Curie-Sklodowska University, Akademicka 19, 20-033 Lublin, Poland.
Adrian ZającDepartment of Functional Anatomy and Cytobiology, Institute of Biological Sciences, Maria Curie-Sklodowska University, Akademicka 19, 20-033 Lublin, Poland.
Ewa GrelaDepartment of Biophysics, Maria Curie-Sklodowska University, Pl. M. Curie-Skłodowskiej 1, 20-031 Lublin, Poland.
Rafał LuchowskiDepartment of Biophysics, Maria Curie-Sklodowska University, Pl. M. Curie-Skłodowskiej 1, 20-031 Lublin, Poland.ORCID 0000-0003-1156-8059
Wiesław I GruszeckiDepartment of Biophysics, Maria Curie-Sklodowska University, Pl. M. Curie-Skłodowskiej 1, 20-031 Lublin, Poland.ORCID 0000-0002-8245-3913
Marta Kinga LemieszekDepartment of Medical Biology, Institute of Rural Health, Jaczewskiego 2, 20-950 Lublin, Poland.
Iwona WertelIndependent Laboratory of Cancer Diagnostics and Immunology, 1st Chair and Department of Oncological Gynaecology and Gynaecology, Medical University of Lublin, Staszica 16, 20-081 Lublin, Poland.ORCID 0000-0003-3396-1679
Łukasz PecioDepartment of Biochemistry and Crop Quality Institute of Soil Science and Plant Cultivation, State Research Institute, Czartoryskich 8, 24-100 Puławy, Poland.ORCID 0000-0002-7407-6716
Jerzy ŻuchowskiDepartment of Biochemistry and Crop Quality Institute of Soil Science and Plant Cultivation, State Research Institute, Czartoryskich 8, 24-100 Puławy, Poland.ORCID 0000-0002-7873-0906
Krystyna Skalicka-WoźniakIndependent Laboratory of Natural Products Chemistry, Medical University of Lublin, Chodzki 1, 20-093 Lublin, Poland.ORCID 0000-0002-9313-5929
Bożena Pawlikowska-PawlęgaDepartment of Functional Anatomy and Cytobiology, Institute of Biological Sciences, Maria Curie-Sklodowska University, Akademicka 19, 20-033 Lublin, Poland.
Monika Hułas-StasiakDepartment of Functional Anatomy and Cytobiology, Institute of Biological Sciences, Maria Curie-Sklodowska University, Akademicka 19, 20-033 Lublin, Poland.
Wojciech RzeskiDepartment of Functional Anatomy and Cytobiology, Institute of Biological Sciences, Maria Curie-Sklodowska University, Akademicka 19, 20-033 Lublin, Poland.ORCID 0000-0002-4511-1498
Radosław RolaDepartment of Neurosurgery and Pediatric Neurosurgery, Medical University of Lublin, Jaczewskiego 8, 20-954 Lublin, Poland.ORCID 0000-0003-0613-6593
Joanna Jakubowicz-GilDepartment of Functional Anatomy and Cytobiology, Institute of Biological Sciences, Maria Curie-Sklodowska University, Akademicka 19, 20-033 Lublin, Poland.ORCID 0000-0003-2077-804X
Maria Curie-Skłodowska University · PLMedical University of Lublin · PLInstitute of Soil Science and Plant Cultivation · PLInstytut Medycyny Wsi im. Witolda Chodźki · PL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

aimThe anti-glioma effect of lensoside Aβ alone and in combination with sorafenib (pro-survival Raf kinase inhibitor) was evaluated for the first time in terms of programmed cell death induction in anaplastic astrocytoma and glioblastoma multiforme cell lines as an experimental model. Apoptosis, autophagy, and necrosis were identified microscopically (fluorescence and scanning microscopes) and confirmed by flow cytometry (mitochondrial membrane potential MMP and cell death). The expression of apoptotic (caspase 3) and autophagic markers (beclin 1) as well as Raf kinase were estimated by immunoblotting. The FTIR method was used to determine the interaction of the studied drugs with lipid and protein groups within cells, while the modes of drug action within the cells were assessed with the FLIM technique.

resultsLensoside Aβ itself does not exhibit anti-glioma activity but significantly enhances the anti-cancer potential of sorafenib, initiating mainly apoptosis of up to 90% of cells. It was correlated with an increased level of active caspase 3, a reduced MMP value, and a lower level of Raf kinase. The interaction with membrane structures led to morphological changes typical of programmed death.

conclusionsOur results indicate that lensoside Aβ plays an important role as an adjuvant in chemotherapy with sorafenib and may be a potential candidate in anti-glioma combination therapy.

Indexed as

apoptosisFLIMFTIRgliomaslensoside AβSEMsorafenib

Identifiers

PMID34072003
PMCPMC8198162
OpenAlexW3165059846

What OpenQuestion 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 OpenQuestion graph.