Evidence map›Paper›PMID 42318338›Full record

ReviewFrontiers in pharmacology2026

Molecularly engineered BODIPY photosensitizers for combined cancer phototherapy and immunotherapy.

Huixia Wang, Yangming Zhang, Mengjiao Zhou

Abstract readReview
In one paragraph

Review in Frontiers in pharmacology, 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

3 authors.

Huixia WangThe People's Hospital of Danyang, Affiliated Danyang Hospital of Nantong University, Danyang, Jiangsu, China.
Yangming ZhangSchool of Pharmacy, Nantong University, Nantong, Jiangsu, China.
Mengjiao ZhouSchool of Pharmacy, Nantong University, Nantong, Jiangsu, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BODIPY-based photosensitizers have attracted great interest in cancer phototherapy and immunotherapy due to their tunable structures, excellent photostability, and high molar extinction coefficients. However, conventional BODIPY dyes have inherent limitations, such as poor water solubility, shallow tissue penetration, oxygen dependence, and insufficient single-modality efficacy. To address these, recent studies have used molecular engineering (ring fusion, electronic modulation, supramolecular assembly, metal coordination) to enhance reactive oxygen species generation and photothermal conversion. Smart delivery systems with microenvironment responsiveness further enable tumor targeting and microenvironment remodeling. Importantly, BODIPY-mediated phototherapy combined with immunotherapeutic strategies (immune checkpoint blockade, pyroptosis/cuproptosis induction, cGAS-STING activation, etc.) achieves synergistic antitumor effects, transforming localized tumor ablation into systemic immunity. This review summarizes recent progress in molecularly engineered BODIPY photosensitizers, from molecular optimization and smart delivery to immune synergy, and discusses current challenges and future directions to promote their clinical translation.

Indexed as

BODIPY photosensitizersimmunotherapyphotodynamic therapyphotothermal therapyreactive oxygen species

Identifiers

PMID42318338
PMCPMC13273039

What OpenQuestion holds

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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.