Evidence map›Paper›PMID 39280423›Full record

ArticleCureus2024

Evaluation of Single and Combined Temozolomide and Doxorubicin Treatment Responses in Low- and High-Grade Glioma In Vitro.

Georgiana Adeline Staicu, Ligia G Tataranu, Daniela Elise Tache, Stefana Oana Popescu, Stefan Alexandru Artene, Suzana Danoiu, Veronica Sfredel, Edmond Nicolae Barcan, Stefania Carina Baloi, Anica Dricu

Abstract read
In one paragraph

Article in Cureus, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

10 authors.

Georgiana Adeline StaicuDepartment of Biochemistry, University of Medicine and Pharmacy of Craiova, Craiova, ROU.
Ligia G TataranuDepartment of Neurosurgery, Bagdasar-Arseni Clinical Emergency Hospital, Bucharest, ROU.
Daniela Elise TacheDepartment of Biochemistry, University of Medicine and Pharmacy of Craiova, Craiova, ROU.
Stefana Oana PopescuDepartment of Biochemistry, University of Medicine and Pharmacy of Craiova, Craiova, ROU.
Stefan Alexandru ArteneDepartment of Biochemistry, University of Medicine and Pharmacy of Craiova, Craiova, ROU.
Suzana DanoiuDepartment of Physiology, University of Medicine and Pharmacy of Craiova, Craiova, ROU.
Veronica SfredelDepartment of Physiology, University of Medicine and Pharmacy of Craiova, Craiova, ROU.
Edmond Nicolae BarcanDepartment of Biochemistry, University of Medicine and Pharmacy of Craiova, Craiova, ROU.
Stefania Carina BaloiDepartment of Biochemistry, University of Medicine and Pharmacy of Craiova, Craiova, ROU.
Anica DricuDepartment of Biochemistry, University of Medicine and Pharmacy of Craiova, Craiova, ROU.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAstrocytoma, the most common type of glioma, can histologically be low or high grade. Treatment recommendations for astrocytic tumors are based on the histopathological and molecular phenotype. For grade 2 astrocytoma, the combination of radiotherapy and adjuvant chemotherapy with procarbazine, lomustine, and vincristine (PCV) is better than radiotherapy alone. Temozolomide (TMZ) is being increasingly recognized as a replacement for PCV in brain tumor therapy, due to the lower myelotoxicity. TMZ is currently a well-established first-line treatment for grade 3 astrocytoma, grade 4 astrocytoma, and glioblastoma and it is also sporadically used for grade 2 astrocytoma. However, TMZ faces multiple challenges such as adverse effects and drug resistance.

methodsIn this study, we compared the cytotoxic effect induced by TMZ and doxorubicin (DOXO), alone and in combination, on a low-grade astrocytoma cell line (AC1B) and a high-grade glioma cell line (GB1B).

resultsWe found that TMZ and DOXO, each produced a cytotoxic effect in monotherapy. GB1B cell line was more sensitive to the treatment than AC1B cells, at a 7- and 10-day exposure to the DOXO. However, when the duration of the treatment was extended to 14 days, GB1B cells became more resistant to DOXO treatment, compared to AC1B cells. Regarding the treatment with TMZ, GB1B exhibited greater resistance to TMZ compared to AC1B, across all studied intervals and the resistance to treatment of GB1B increased with longer exposure time. However, in combined therapy, the drugs did not exert a synergistic effect on any astrocytic cell line.

conclusionsThe current data suggest that both TMZ and DOXO exhibit efficient therapeutic effects on low- and high-grade glioma cells. However, no synergistic effect was observed for combined therapy.

Indexed as

astrocytomacytotoxicitydoxorubicinglioblastomatemozolomide

Identifiers

PMID39280423
PMCPMC11401637

What Socratic holds

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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.