Evidence map›Paper›PMID 36174026›Full record

ArticlePloS one2022

Metronomic doses and drug schematic combination response tested within chambered coverslips for the treatment of breast cancer cells (JIMT-1).

Gustavo Rosero, Gisela Pattarone, Ana Peñaherera, Julia Pilz, Joschka Bödecker, Maximiliano Perez, Roland Mertelsmann, Betiana Lerner, Marie Follo

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2022. 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
0.1field-weighted citation impact, top 52% of its field
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 citations in OpenAlex.

  1. Review
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 at 3 institutions in 3 countries.

Gustavo RoseroNational Technological University (UTN) IREN Center, Buenos Aires, Argentina.
Gisela PattaroneFaculty of Medicine, Department of Medicine I, Medical Center-University of Freiburg, University of Freiburg, Freiburg, Germany.
Ana PeñahereraNational Technological University (UTN) IREN Center, Buenos Aires, Argentina.
Julia PilzFaculty of Medicine, Department of Medicine I, Medical Center-University of Freiburg, University of Freiburg, Freiburg, Germany.
Joschka BödeckerFaculty of Engineering, Neurorobotics Lab, Computer Science Department, University of Freiburg, Georges-Köhler-Allee, Freiburg, Germany.
Maximiliano PerezNational Technological University (UTN) IREN Center, Buenos Aires, Argentina.
Roland MertelsmannFaculty of Medicine, Department of Medicine I, Medical Center-University of Freiburg, University of Freiburg, Freiburg, Germany.
Betiana LernerFaculty of Engineering, University of Buenos Aires (UBA), Institute of Engineering Biomedical, Buenos Aires, Argentina.ORCID 0000-0003-3341-5686
Marie FolloFaculty of Medicine, Department of Medicine I, Medical Center-University of Freiburg, University of Freiburg, Freiburg, Germany.
University of Freiburg · DENational Technological University · ARFlorida International University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Low-dose metronomic (LDM) chemotherapy is an alternative to conventional chemotherapy and is the most frequently used approach in low dose chemotherapy regimens. The selection of patients, drug dosages, and dosing intervals in LDM is empirical. In this study, we systematically examined the schedule-dependent interaction of drugs on a breast cancer cell line (BCC) cultured in chambered coverslips. The LDM studies were combined with cell staining in order to better characterize different cell states and cell death modes, including caspase-dependent apoptosis, caspase-independent cell death and autophagy-dependent cell death. Microscope images were examined using the Fiji Trainable Weka Segmentation plugin to analyse cell area in 7500 images showing different modes of cell death. Paclitaxel combined with LDM chemotherapy demonstrated a reduction in the area covered by live cells. In contrast, there was an induction of high levels of cell death due to caspase-dependent apoptosis.

Indexed as

Breast NeoplasmsApoptosisCaspasesDrug CombinationsFemaleHumansPaclitaxelCaspasesDrug CombinationsPaclitaxel

Identifiers

PMID36174026
PMCPMC9522273
OpenAlexW4297991414

What OpenQuestion holds

Textmetadata
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.