Evidence map›Paper›PMID 26282350›Full record

ArticleScientific reports2015

ABCG2 transporter inhibitor restores the sensitivity of triple negative breast cancer cells to aminolevulinic acid-mediated photodynamic therapy.

Pratheeba Palasuberniam, Xue Yang, Daniel Kraus, Patrick Jones, Kenneth A Myers, Bin Chen

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 47 papers.

0numbers the graph read from it
0cells of the map it votes in
47citing papers in PubMed
4.3field-weighted citation impact, top 5% 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

47 citing papers in PubMed, 87 citations in OpenAlex.

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  11. Cancer Cell-Specific Fluorescent Prodrug Delivery Platforms.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2023
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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

6 authors at 1 institution in 1 country.

Pratheeba PalasuberniamDepartment of Pharmaceutical Sciences, Philadelphia College of Pharmacy, University of the Sciences, Philadelphia, Pennsylvania, USA.
Xue YangDepartment of Pharmaceutical Sciences, Philadelphia College of Pharmacy, University of the Sciences, Philadelphia, Pennsylvania, USA.
Daniel KrausDepartment of Pharmaceutical Sciences, Philadelphia College of Pharmacy, University of the Sciences, Philadelphia, Pennsylvania, USA.
Patrick JonesDepartment of Biological Sciences, Misher College of Arts &Sciences, University of the Sciences, Philadelphia, Pennsylvania, USA.
Kenneth A MyersDepartment of Biological Sciences, Misher College of Arts &Sciences, University of the Sciences, Philadelphia, Pennsylvania, USA.
Bin ChenDepartment of Pharmaceutical Sciences, Philadelphia College of Pharmacy, University of the Sciences, Philadelphia, Pennsylvania, USA.
University of the Sciences · US

Funding

Regulation of Endothelial Cell Branching Morphogenesis via MCAK-targted ControlK22HL113069 · NHLBI · UNIVERSITY OF THE SCIENCES PHILADELPHIA · PI MYERS, KENNETH ALBERT · 2013 to 2015
$720k
NHLBI NIH HHS K22 HL113069
6 · The paper itself

Abstract

Photosensitizer protoporphyrin IX (PpIX) fluorescence, intracellular localization and cell response to photodynamic therapy (PDT) were analyzed in MCF10A normal breast epithelial cells and a panel of human breast cancer cells including estrogen receptor (ER) positive, human epidermal growth factor receptor 2 (HER2) positive and triple negative breast cancer (TNBC) cells after treatment with PpIX precursor aminolevulinic acid (ALA). Although PpIX fluorescence was heterogeneous in different cells, TNBC cells showed significantly lower PpIX level than MCF10A and ER- or HER2-positive cells. PpIX fluorescence in TNBC cells also had much less mitochondrial localization than other cells. There was an inverse correlation between PpIX fluorescence and cell viability after PDT. Breast cancer cells with the highest PpIX fluorescence were the most sensitive to ALA-PDT and TNBC cells with the lowest PpIX level were resistant to PDT. Treatment of TNBC cells with ABCG2 transporter inhibitor Ko143 significantly increased ALA-PpIX fluorescence, enhanced PpIX mitochondrial accumulation and sensitized cancer cells to ALA-PDT. Ko143 treatment had little effect on PpIX production and ALA-PDT in normal and ER- or HER2-positive cells. These results demonstrate that enhanced ABCG2 activity renders TNBC cell resistance to ALA-PDT and inhibiting ABCG2 transporter is a promising approach for targeting TNBC with ALA-based modality.

Indexed as

AdenosineATP-Binding Cassette TransportersATP Binding Cassette Transporter, Subfamily G, Member 2Cell Line, TumorCell SurvivalDiketopiperazinesDose-Response Relationship, DrugDose-Response Relationship, RadiationDrug SynergismHeterocyclic Compounds, 4 or More RingsHumansLightMalonatesNeoplasm ProteinsPhotochemotherapyPhotosensitizing Agents3-(6-isobutyl-9-methoxy-1,4-dioxo-1,2,3,4,6,7,12,12a-octahydropyrazino(1',2'-1,6)pyrido(3,4-b)indol-3-yl)propionic acid tert-butyl esterABCG2 protein, humanAdenosineaminomalonic acidATP-Binding Cassette TransportersATP Binding Cassette Transporter, Subfamily G, Member 2DiketopiperazinesHeterocyclic Compounds, 4 or More RingsMalonatesNeoplasm ProteinsPhotosensitizing Agents

Identifiers

PMID26282350
PMCPMC4539603
OpenAlexW2419531088

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.