Evidence map›Paper›PMID 41979748›Full record

ArticlePlant foods for human nutrition (Dordrecht, Netherlands)2026

Gastrointestinal Digestion Enhances the In vitro Antitumor Activity of Red Grape Anthocyanins Against Colorectal Cancer Cells.

Daniel Cruceriu, Denisa Dobos, Stefan Miron, Oana Baldasici, Loredana Balacescu, Ovidiu Balacescu, Zorita Diaconeasa

Abstract read
In one paragraph

Article in Plant foods for human nutrition (Dordrecht, Netherlands), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Rambutan (Molecules (Basel, Switzerland) · 2026
    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

7 authors.

Daniel CruceriuDepartment of Genetics, Genomics and Experimental Pathology, The Oncology Institute "Prof. Dr. Ion Chiricuta", 34-36 Republicii Street, Cluj-Napoca, 400015, Romania.
Denisa DobosDepartment of Genetics, Genomics and Experimental Pathology, The Oncology Institute "Prof. Dr. Ion Chiricuta", 34-36 Republicii Street, Cluj-Napoca, 400015, Romania.
Stefan MironDepartment of Genetics, Genomics and Experimental Pathology, The Oncology Institute "Prof. Dr. Ion Chiricuta", 34-36 Republicii Street, Cluj-Napoca, 400015, Romania.
Oana BaldasiciDepartment of Genetics, Genomics and Experimental Pathology, The Oncology Institute "Prof. Dr. Ion Chiricuta", 34-36 Republicii Street, Cluj-Napoca, 400015, Romania.
Loredana BalacescuDepartment of Genetics, Genomics and Experimental Pathology, The Oncology Institute "Prof. Dr. Ion Chiricuta", 34-36 Republicii Street, Cluj-Napoca, 400015, Romania.
Ovidiu BalacescuDepartment of Genetics, Genomics and Experimental Pathology, The Oncology Institute "Prof. Dr. Ion Chiricuta", 34-36 Republicii Street, Cluj-Napoca, 400015, Romania.
Zorita DiaconeasaFaculty of Food Science and Technology, University of Agricultural Science and Veterinary Medicine, 3-5 Calea Manastur Street, Cluj- Napoca, 400372, Romania. zorita.sconta@usamvcluj.ro.

Funding

Romanian National Authority for Scientific Research (UEFISCDI) PN-III-P1-1.1-TE-2019-0960, 178TE/2020.
6 · The paper itself

Abstract

Anthocyanins from red grapes possess notable anticancer properties, yet their biological activity after gastrointestinal digestion remains poorly characterized. In this study, we investigated the in vitro antitumor effects of a red grape anthocyanin extract digested using the INFOGEST protocol on colorectal cancer (CRC) cell lines. The study assessed cell viability, apoptosis induction, cell cycle progression, and confined 3D migration, and integrated whole-transcriptome microarray profiling to elucidate the underlying molecular mechanisms.Cell viability assays showed that simulated digestion markedly increased the extract’s potency, reducing the IC50 values by 2.25-fold in DLD1 cells and 1.59-fold in Caco2 cells. Transcriptomic profiling by microarray analysis demonstrated substantial gene expression changes upon treatment in DLD1 cells, with 873 genes showing a fold regulation greater than |±1.5|. Gene Set Enrichment Analysis (GSEA) identified enrichment of pro-apoptotic gene sets in treated cells, including p53 signaling, prolonged unfolded protein response activation and suppression of RNA metabolism. These findings were supported by the Annexin V/PI assay demonstrating apoptosis induction, and RT-qPCR validation of key apoptosis-regulating genes. The extract also displayed significant antiproliferative activity with cells arrested in the S phase, as evidenced by AlamarBlue and cell cycle analyses. Downregulation of key cell cycle promoters and upregulation of proliferation-inhibitory genes were also observed. Furthermore, the extract significantly impaired 3D migration in a microfluidic model, reducing migration speed, directionality, and number of migratory cells. GSEA revealed suppression of RHO GTPases and MIRO-mediated signaling, suggesting disruption of cytoskeletal and mitochondrial dynamics, strongly impacting cell migration. Together, these findings indicate that digested red grape anthocyanins exert a multifaceted anticancer effect in vitro by promoting apoptosis, inhibiting proliferation, and impairing cell migration, highlighting their potential as functional bioactive compounds for CRC management.

Indexed as

AnthocyaninsAntineoplastic Agents, PhytogenicColorectal NeoplasmsDigestionPlant ExtractsVitisApoptosisCaco-2 CellsCell CycleCell Line, TumorCell MovementCell ProliferationCell SurvivalGene Expression ProfilingHumansAnthocyaninsAntineoplastic Agents, PhytogenicPlant ExtractsApoptosisCell cycle arrestCell migrationColorectal cancerINFOGEST digestionRed grape anthocyaninsTranscriptomics

Identifiers

PMID41979748
PMCPMC13079503

What OpenQuestion holds

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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.