Evidence map›Paper›PMID 41831451›Full record

ArticleEuropean journal of dentistry2026

Ethanol Extract of Catharanthus roseus Leaves Exhibits Anticancer Effects on HSC-3 Tongue Cancer Cells Associated with PI3K Suppression and PARP Cleavage.

Ferry Sandra, Melanie Sadono Djamil, Muhammad Ihsan Rizal, Ria Aryani Hayuningtyas, Jackson Dipankara, Nur'amalia Isnaeni, Samuel Ryan Krisdianto, Kerinillia Mochtar, Kyung Hoon Lee

Abstract read
In one paragraph

Article in European journal of dentistry, 2026. 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

9 authors.

Ferry SandraDepartment of Biochemistry and Molecular Biology, Division of Oral Biology, Faculty of Dentistry, Universitas Trisakti, Indonesia.ORCID 0000-0002-5852-1074
Melanie Sadono DjamilDepartment of Biochemistry and Molecular Biology, Division of Oral Biology, Faculty of Dentistry, Universitas Trisakti, Indonesia.
Muhammad Ihsan RizalDepartment of Biochemistry and Molecular Biology, Division of Oral Biology, Faculty of Dentistry, Universitas Trisakti, Indonesia.ORCID 0000-0002-2370-038X
Ria Aryani HayuningtyasDepartment of Biochemistry and Molecular Biology, Division of Oral Biology, Faculty of Dentistry, Universitas Trisakti, Indonesia.
Jackson DipankaraDepartment of Oral and Maxillofacial Surgery, Faculty of Dentistry, Universitas Trisakti, Jakarta, Indonesia.
Nur'amalia IsnaeniFaculty of Dentistry, Universitas Trisakti, Jakarta, Indonesia.
Samuel Ryan KrisdiantoFaculty of Dentistry, Universitas Trisakti, Jakarta, Indonesia.
Kerinillia MochtarFaculty of Dentistry, Universitas Trisakti, Jakarta, Indonesia.
Kyung Hoon LeeResearch Institute, Ballys Co. Ltd, Incheon, Republic of Korea.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Objective: Tongue cancer represents nearly half of all oral cancer cases globally, necessitating the exploration of novel therapeutic agents. Materials and Methods: Cells were treated with various concentrations of EECRL. Cell viability was assessed using the MTT assay, apoptosis was evaluated by sub-G1 analysis, and levels of cleaved-PARP and phosphorylated PI3K were measured using enzyme-linked immunosorbent assay. Statistical Analysis: Data normality was assessed using the Shapiro-Wilk test. Depending on data distribution, comparisons were performed using one-way analysis of variance followed by Tukey's post hoc test or the Kruskal-Wallis test followed by Dunn's post hoc test. Correction for multiple comparisons was applied using the Holm-Bonferroni method, and adjusted Results: EECRL reduced number of viable cells and induced apoptosis in HSC-3 cells in a significant, concentration-dependent manner (adjusted Conclusion: EECRL reduced viable cell numbers and induced apoptotic features in HSC-3 tongue cancer cells, with effects associated with suppression of PI3K signaling and increased PARP cleavage. These findings suggest that EECRL may have potential as an alternative therapeutic candidate for tongue cancer. However, further mechanistic studies are required to confirm causal pathway involvement.

Identifiers

PMID41831451
PMCPMC13337269

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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 OpenQuestion graph.