Evidence map›Paper›PMID 26625309›Full record

ArticleOncotarget2015

Stimulation of dendritic cells by DAMPs in ALA-PDT treated SCC tumor cells.

Xiaojie Wang, Jie Ji, Haiyan Zhang, Zhixia Fan, Linglin Zhang, Lei Shi, Feifan Zhou, Wei R Chen, Hongwei Wang, Xiuli Wang

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 40 papers.

0numbers the graph read from it
0cells of the map it votes in
40citing papers in PubMed
4.8field-weighted citation impact, top 4% 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

40 citing papers in PubMed, 87 citations in OpenAlex.

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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

10 authors at 3 institutions in 2 countries.

Xiaojie WangShanghai Skin Disease Hospital, Shanghai 200443, China.
Jie JiShanghai Skin Disease Hospital, Shanghai 200443, China.
Haiyan ZhangShanghai Skin Disease Hospital, Shanghai 200443, China.
Zhixia FanShanghai Skin Disease Hospital, Shanghai 200443, China.
Linglin ZhangShanghai Skin Disease Hospital, Shanghai 200443, China.
Lei ShiShanghai Skin Disease Hospital, Shanghai 200443, China.
Feifan ZhouBiophotonics Research Laboratory, Center for Interdisciplinary Biomedical Education and Research, University of Central Oklahoma, Edmond, OK 73034, USA.
Wei R ChenBiophotonics Research Laboratory, Center for Interdisciplinary Biomedical Education and Research, University of Central Oklahoma, Edmond, OK 73034, USA.
Hongwei WangHuadong Hospital, Fudan University, Shanghai 200040, China.
Xiuli WangShanghai Skin Disease Hospital, Shanghai 200443, China.
Shanghai Skin Disease Hospital · CNFudan University · CNUniversity of Central Oklahoma · US

Funding

NIBIB NIH HHS R21 EB0155091-01
6 · The paper itself

Abstract

Photodynamic therapy (PDT) not only kills tumor cells directly but also rapidly recruits and activates immune cells favoring the development of antitumor adaptive immunity. It is believed that Topical 5-aminolevulinic acid mediated photodynamic therapy (ALA-PDT) can induce anti-tumor immune responses through dangerous signals damage-associated molecular patterns (DAMPs). In this study, we investigated the effect of ALA-PDT induced DAMPs on immune cells. We focused on the stimulation of dendritic cells by major DAMPs, enhanced the expression of calreticulin (CRT), heat shock proteins 70 (HSP70), and high mobility group box 1 (HMGB1), either individually or in combination. We evaluated in vitro and in vivo expressions of DAMPs induced by ALA-PDT using immunohistochemistry, western blot, and ELISA in a squamous cell carcinoma (SCC) mouse model. The role of DAMPs in the maturation of DCs potentiated by ALA-PDT-treated tumor cells was detected by FACS and ELISA. Our results showed that ALA-PDT enhanced the expression of CRT, HSP70, and HMGB1. These induced DAMPs played an important part in activating DCs by PDT-treated tumor cells, including phenotypic maturation (increase of surface expression of MHC-II, CD80, and CD86) and functional maturation (enhanced capability to secrete IFN-γ and IL-12). Furthermore, injecting ALA-PDT-treated tumor cells into naïve mice resulted in complete protection against cancer cells of the same origin. Our findings indicate that ALA-PDT can increase DAMPs and enhance tumor immunogenicity, providing a promising strategy for inducing a systemic anticancer immune response.

Indexed as

PhotochemotherapyAminolevulinic AcidAnimalsCalreticulinCancer VaccinesCarcinoma, Squamous CellCytokinesDendritic CellsFemaleHMGB1 ProteinHSP70 Heat-Shock ProteinsMiceNeoplasm TransplantationPhenotypePhotosensitizing AgentsReceptors, ImmunologicAminolevulinic AcidCalreticulinCancer VaccinesCytokinesHMGB1 ProteinHMGB1 protein, mouseHSP70 Heat-Shock ProteinsPhotosensitizing AgentsReceptors, Immunologic5-aminolevulinic acid mediated photodynamic therapydanger-associated molecular patternsdendritic cellsimmune responsessquamous cell carcinoma

Identifiers

PMID26625309
PMCPMC4792585
OpenAlexW2212950451

What OpenQuestion holds

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LicenceCC BY
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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.