Evidence map›Paper›PMID 41085789›Full record

ArticleDiscover oncology2025

In vitro assessment of benzothiadiazole-based photoactive polymers against ovarian, prostate and bladder cancer cell lines for photodynamic therapy.

Rolan Mansour, Fawziye Tarhini, Nicolas Bruce, Jamie Blanche, Mahmoud Wagih, Ahmad Taha, Karin Williams, Jonathan Copper, Muhammad Imran, Karin Oien and 2 more

Abstract read
In one paragraph

Article in Discover oncology, 2025. 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

12 authors.

Rolan MansourJames Watt School of Engineering, University of Glasgow, Glasgow, G12 8QQ, UK. Rolan.mansour@glasgow.ac.uk.
Fawziye TarhiniJames Watt School of Engineering, University of Glasgow, Glasgow, G12 8QQ, UK.
Nicolas BruceJames Watt School of Engineering, University of Glasgow, Glasgow, G12 8QQ, UK.
Jamie BlancheJames Watt School of Engineering, University of Glasgow, Glasgow, G12 8QQ, UK.
Mahmoud WagihJames Watt School of Engineering, University of Glasgow, Glasgow, G12 8QQ, UK.
Ahmad TahaJames Watt School of Engineering, University of Glasgow, Glasgow, G12 8QQ, UK.
Karin WilliamsSchool of Cancer Sciences, University of Glasgow, Glasgow, G61 1QH, UK.
Jonathan CopperJames Watt School of Engineering, University of Glasgow, Glasgow, G12 8QQ, UK.
Muhammad ImranJames Watt School of Engineering, University of Glasgow, Glasgow, G12 8QQ, UK.
Karin OienSchool of Cancer Sciences, University of Glasgow, Glasgow, G61 1QH, UK.
Hadi HeidariJames Watt School of Engineering, University of Glasgow, Glasgow, G12 8QQ, UK.
David FlynnJames Watt School of Engineering, University of Glasgow, Glasgow, G12 8QQ, UK.

Funding

Engineering and Physical Sciences Research Council EP/X017516/1
6 · The paper itself

Abstract

There are unmet clinical needs of bladder cancer associated with its late detection, limited treatment options, and high mortality rate. In response to this, we present the results of the in-vitro assessment of photodynamic polymers, prior to their integration into a wireless biomedical implant for in-situ photodynamic therapy (PDT). PDT selectively activates light-sensitive photosensitizers, to kill cancer cells without the adverse effects associated with systemic therapies, such as chemotherapy. PDT offers significant advantages in hypoxic tumors, including oxygen-independent cytotoxicity known to impede the curative efficiency of radiotherapy. Accordingly, we report on the design methodology and microfabrication process of an in-situ PDT wireless microsystem as a novel treatment modality. We present the preliminary results from three benzothiadiazole-based polymers that are evaluated as solid support photosensitizers for the inhibition of cancer growth in three cell lines. Cell lines represent ovarian, prostate and bladder cancer, the reduction in cell number was assessed with Sulforhodamine B assays. Following Polyamide, aminophenyl- (PA-ABT) treatment, cells were subjected to a range of 420 nm light exposures and fluorimetry was used to determine cell growth. PA-ABT was shown to cause growth inhibition only at higher concentrations in all tested cell lines. PA-ABT can be considered as a promising candidate for in-situ PDT treatment due to its inhibitory effects in cancer cell lines open new possibilities for mono or combination light-based therapy in cancer treatment for previously inaccessible cancers.

Indexed as

Biomedical technologyCancer therapyMaterialsMicrosystemPhotodynamic therapy (PDT)Photosensitizers

Identifiers

PMID41085789
PMCPMC12521685

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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.