Evidence map›Paper›PMID 42791928›Full record

ArticleBioengineering (Basel, Switzerland)2026

Parameter-Dependent Electroporation and Cellular Responses Induced by Microsecond Pulsed Electric Fields: Different Sensitivity of Two Pancreatic Ductal Adenocarcinoma Cell Lines.

Mariateresa Allocca, Stefania Romeo, Maria Rosaria Scarfì, Olga Zeni, Anna Sannino, Giuseppina Palmiero, Sanober Kafeel, Angela Ragone, Silvio Naviglio, Luigi Sapio

Abstract read
In one paragraph

Article in Bioengineering (Basel, Switzerland), 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

10 authors.

Mariateresa AlloccaInstitute for Electromagnetic Sensing of the Environment (IREA), CNR, Via Diocleziano 320, 80124 Napoli, Italy.ORCID 0000-0003-3693-2515
Stefania RomeoInstitute for Electromagnetic Sensing of the Environment (IREA), CNR, Via Diocleziano 320, 80124 Napoli, Italy.ORCID 0000-0002-9849-3637
Maria Rosaria ScarfìInstitute for Electromagnetic Sensing of the Environment (IREA), CNR, Via Diocleziano 320, 80124 Napoli, Italy.ORCID 0000-0002-9308-6928
Olga ZeniInstitute for Electromagnetic Sensing of the Environment (IREA), CNR, Via Diocleziano 320, 80124 Napoli, Italy.ORCID 0000-0002-2432-2384
Anna SanninoInstitute for Electromagnetic Sensing of the Environment (IREA), CNR, Via Diocleziano 320, 80124 Napoli, Italy.ORCID 0000-0003-0009-4644
Giuseppina PalmieroDepartment of Precision Medicine, University of Campania "Luigi Vanvitelli", Via L. De Crecchio 7, 80138 Napoli, Italy.ORCID 0009-0006-0300-0307
Sanober KafeelDepartment of Precision Medicine, University of Campania "Luigi Vanvitelli", Via L. De Crecchio 7, 80138 Napoli, Italy.ORCID 0000-0003-1282-6347
Angela RagoneDepartment of Precision Medicine, University of Campania "Luigi Vanvitelli", Via L. De Crecchio 7, 80138 Napoli, Italy.ORCID 0000-0001-9229-4146
Silvio NaviglioDepartment of Precision Medicine, University of Campania "Luigi Vanvitelli", Via L. De Crecchio 7, 80138 Napoli, Italy.ORCID 0000-0003-1771-8265
Luigi SapioDepartment of Precision Medicine, University of Campania "Luigi Vanvitelli", Via L. De Crecchio 7, 80138 Napoli, Italy.ORCID 0000-0001-6774-9815

Funding

Ministry of Universities and Research 960.30-06-2023
6 · The paper itself

Abstract

Pancreatic ductal adenocarcinoma (PDAC) is a highly aggressive, treatment-resistant tumor requiring novel therapeutic approaches. Electroporation (EP)-based strategies are promising tools for local tumor control and enhanced drug delivery. However, cellular responses and protocols optimization remain poorly investigated in PDAC. Here, we investigated the effects of variable microsecond pulsed electric fields (PEFs) on PANC-1 and MIA PaCa-2 PDAC cells. Immediate responses were assessed via membrane permeabilization and cell death. Delayed effects were evaluated through viability, growth, cell cycle and expression of stress markers. Immediate cell death occurred above specific thresholds in PANC-1 and MIA PaCa-2 cells (16 pulses at 1 kV/cm and 30 pulses at 2.5 kV/cm, respectively), suggesting differential sensitivity to PEFs. Delayed analyses confirmed differences in both viability (-19.3% vs. -46.4% with 4 pulses, 1 kV/cm, 48 h) and growth (-30.3% vs. -57.6% with 4 pulses, 1 kV/cm, 48 h). An opposite modulation of the S-phase population was also observed at 48 h (+7.4% with 20 pulses at 1 kV/cm and -9.2% with 8 pulses at 1 kV/cm for PANC-1 and MIA PaCa-2, respectively). Both cell lines showed similar regulations of apoptosis-associated and autophagy-related markers. Overall, PEFs elicited parameter- and cell-specific responses, supporting fine-tuned EP protocols for pancreatic cancer therapy.

Indexed as

cellular stress responseirreversible electroporationpancreatic ductal adenocarcinoma cellspulsed electric fieldsreversible electroporation

Identifiers

PMID42791928
PMCPMC13603243

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Registered trials

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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.