Evidence map›Paper›PMID 42331942›Full record

ArticleScientific reports2026

Anticancer activity with physical property analysis of Mollugo cerviana (L). Ser whole plant extract on hepatocellular carcinoma cell lines (HepG2).

Sherin Rebecca Flavian, Ramanathan Sharmila, Sahaya Vijay Jeyaraj, Fikadu Tesgera Tolasa, Rajamanickam Pon Nivedha, Tony Augustine, Janani Ezhilan, Sagni Ragassa Wadajo

Abstract read
In one paragraph

Article in Scientific reports, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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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

8 authors.

Sherin Rebecca FlavianPG and Research Department of Biotechnology, Bishop Heber College (Autonomous), Bharathidasan University, Tiruchirappalli, 620017, India.
Ramanathan SharmilaPG and Research Department of Biotechnology, Bishop Heber College (Autonomous), Bharathidasan University, Tiruchirappalli, 620017, India.
Sahaya Vijay JeyarajSchool of Advanced Sciences, Vellore Institute of Technology, Vellore, 632014, India.
Fikadu Tesgera TolasaDepartment of Mathematics, Dambi Dollo University, Oromia, Ethiopia. fikadu@dadu.edu.et.
Rajamanickam Pon NivedhaPG and Research Department of Biotechnology and Bioinformatics, Holy Cross College (Autonomous), Tiruchirappalli, India.
Tony AugustineDepartment of Mathematics, Nirmala College (Autonomous), Muvattupuzha, Ernakulam, Kerala, 686661, India.
Janani EzhilanSchool of Advanced Sciences, Vellore Institute of Technology, Vellore, 632014, India.
Sagni Ragassa WadajoSchool of Veterinary Medicine, Dambi Dollo University, Oromia, Ethiopia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Hepatocellular carcinoma is a rapidly advancing malignancy and remains a leading cause of cancer-related mortality. Recently, plant-based pharmaceuticals have garnered increased attention compared to synthetic medications due to their non-toxic nature and accessibility. Mollugo cerviana, a prevalent weed in the Mollugnaceae family, is recognised for its antioxidant and anti-inflammatory properties. The ethanolic extract of the plant was evaluated for its cytotoxic effects on hepatocarcinoma cell lines (HepG2). The vitality of the treated cells was evaluated using the MTT test. The induction of oxidative stress was assessed by quantifying intracellular reactive oxygen species (ROS) levels and the mechanism of cell death was analysed using ethidium bromide/acridine orange (EB/AO) dual staining. Additionally, the DNA damage was assessed via the comet test. To ascertain the probable bioactive chemicals responsible for the observed cytotoxicity, LC-MS analysis of the plant extract was conducted. The primary components found in the plant extract underwent molecular descriptor analysis and statistical correlations were established to evaluate their notable drug-likeness and possible therapeutic significance. The plant extract induces cell death in a dose-dependent manner, as demonstrated by the MTT assay, with HepG2 cell viability decreasing from 98 to 44% at concentrations ranging from 1 to 500 µg/mL. HepG2 cells exposed to 356.03 µg/ml (IC

Indexed as

Antineoplastic Agents, PhytogenicCarcinoma, HepatocellularLiver NeoplasmsPlant ExtractsApoptosisCell SurvivalDNA DamageHep G2 CellsHumansOxidative StressReactive Oxygen SpeciesAntineoplastic Agents, PhytogenicPlant ExtractsReactive Oxygen Species

Identifiers

PMID42331942
PMCPMC13572517

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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.