Evidence map›Paper›PMID 39395619›Full record

ArticlePhotodiagnosis and photodynamic therapy2024

Efficacy of photodynamic therapy using 5-aminolevulinic acid-induced photosensitization is enhanced in pancreatic cancer cells with acquired drug resistance.

Yiran Liu, Sally Kyei Mensah, Sergio Farias, Shakir Khan, Tayyaba Hasan, Jonathan P Celli

Abstract read
In one paragraph

Article in Photodiagnosis and photodynamic therapy, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Review
  2. Article
  3. 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

6 authors.

Yiran LiuDepartment of Physics, University of Massachusetts Boston, 100 Morrissey Blvd, Boston, MA 02125, USA.
Sally Kyei MensahDepartment of Physics, University of Massachusetts Boston, 100 Morrissey Blvd, Boston, MA 02125, USA.
Sergio FariasDepartment of Physics, University of Massachusetts Boston, 100 Morrissey Blvd, Boston, MA 02125, USA.
Shakir KhanDepartment of Physics, University of Massachusetts Boston, 100 Morrissey Blvd, Boston, MA 02125, USA; Wellman Center for Photomedicine, Massachusetts General Hospital, 40 Blossom St, Boston, MA 02114, USA.
Tayyaba HasanWellman Center for Photomedicine, Massachusetts General Hospital, 40 Blossom St, Boston, MA 02114, USA.
Jonathan P CelliDepartment of Physics, University of Massachusetts Boston, 100 Morrissey Blvd, Boston, MA 02125, USA; Wellman Center for Photomedicine, Massachusetts General Hospital, 40 Blossom St, Boston, MA 02114, USA; Center for Personalized Cancer Therapy, University of Massachusetts Boston, 100 Morrissey Blvd, Boston, MA 02125, USA. Electronic address: jonathan.celli@umb.edu.

Funding

UMass Boston-DF/HCC U54 Partnership (2 of 2)U54CA156734 · NCI · UNIVERSITY OF MASSACHUSETTS BOSTON · PI Jan Mutchler · 2010 to 2026
$24.9M
Initiative for Maximizing Student Diversity at UMass BostonR25GM076321 · NIGMS · UNIVERSITY OF MASSACHUSETTS BOSTON · PI COLON-CARMONA, ADAN, SKVIRSKY, RACHEL · 2008 to 2022
$4.5M
Low-cost Enabling Technology for Image-guided Photodynamic Therapy (PDT) of OralUH3CA189901 · NCI · MASSACHUSETTS GENERAL HOSPITAL · PI CELLI, JONATHAN P, HASAN, TAYYABA · 2016 to 2019
$2.7M
A comprehensive platform for low-cost screening and image-guided photodynamic therapy (PDT) of pre-malignant and malignant oral lesions in low resource settingsU01CA279862 · NCI · UNIVERSITY OF MASSACHUSETTS BOSTON · PI Jonathan P Celli, Tayyaba Hasan · 2023 to 2026
$2.4M
Mechanism-based therapies for pancreatic cancer informed by stromal microrheologyR00CA155045 · NCI · UNIVERSITY OF MASSACHUSETTS BOSTON · PI CELLI, JONATHAN P · 2013 to 2015
$708k
NCI NIH HHS R00 CA155045NCI NIH HHS U01 CA279862NCI NIH HHS U54 CA156734NCI NIH HHS UH3 CA189901NIGMS NIH HHS R25 GM076321
6 · The paper itself

Abstract

The use of 5-aminolevulinic acid (ALA) as a precursor for protoporphyrin IX (PpIX) is an established photosensitization strategy for photodynamic therapy (PDT) and fluorescence guided surgery. Ongoing studies are focused on identifying approaches to enhance PpIX accumulation as well as to identify tumor sub-types associated with high PpIX accumulation. In this study, we investigated PpIX accumulation and PDT treatment response with respect to nodule size in 3D cultures of pancreatic cancer cells (Panc1) and a derivative subline (Panc1OR), which has acquired drug resistance and exhibits increased epithelial mesenchymal transition. In monolayer and 3D culture dose response studies the Panc1OR cells exhibit significantly a higher level of photokilling at lower light doses than the drug naïve cells. Panc1OR also exhibits increased PpIX accumulation. Further analysis of cell killing efficiency per molecule of intracellular PpIX indicates that the drug resistant cells are intrinsically more responsive to PDT. Additional investigation using exogenous delivery of PpIX also shows higher cell killing in drug resistant cells, under conditions which achieve approximately the same intracellular PpIX. Overall these results are significant as they demonstrate that this example of drug-resistant cells associated with aggressive disease progression and poor clinical outcomes, show increased sensitivity to ALA-PDT.

Indexed as

Aminolevulinic AcidDrug Resistance, NeoplasmPancreatic NeoplasmsPhotochemotherapyPhotosensitizing AgentsProtoporphyrinsCell Line, TumorCell SurvivalDose-Response Relationship, DrugHumansAminolevulinic AcidPhotosensitizing Agentsprotoporphyrin IXProtoporphyrins3D cell culture5-aminolevulinic acid (ALA)Drug resistancePancreatic cancerPhotodynamic therapy (PDT)Protoporphyrin IX (PpIX)

Identifiers

PMID39395619
PMCPMC11645186

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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.