Evidence map›Paper›PMID 31460395›Full record

ArticleACS omega2019

Artificial Cell-Mediated Photodynamic Therapy Enhanced Anticancer Efficacy through Combination of Tumor Disruption and Immune Response Stimulation.

Jiang Ni, Ying Sun, Jinfang Song, Yiqing Zhao, Qiufang Gao, Xia Li

Open access · goldAbstract read
In one paragraph

Article in ACS omega, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.3field-weighted citation impact, top 21% 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

6 citing papers in PubMed, 19 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
  4. Article
  5. Article
  6. 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 at 1 institution in 1 country.

Jiang NiDepartment of Pharmacy, The Affiliated Hospital of Jiangnan University (original Area of Wuxi Third People's Hospital), No. 585, North Xingyuan Road, Liang Xi District, Wuxi City 214000, Jiangsu Province, P. R. China.
Ying SunDepartment of Pharmacy, The Affiliated Hospital of Jiangnan University (original Area of Wuxi Third People's Hospital), No. 585, North Xingyuan Road, Liang Xi District, Wuxi City 214000, Jiangsu Province, P. R. China.
Jinfang SongDepartment of Pharmacy, The Affiliated Hospital of Jiangnan University (original Area of Wuxi Third People's Hospital), No. 585, North Xingyuan Road, Liang Xi District, Wuxi City 214000, Jiangsu Province, P. R. China.
Yiqing ZhaoDepartment of Pharmacy, The Affiliated Hospital of Jiangnan University (original Area of Wuxi Third People's Hospital), No. 585, North Xingyuan Road, Liang Xi District, Wuxi City 214000, Jiangsu Province, P. R. China.
Qiufang GaoDepartment of Pharmacy, The Affiliated Hospital of Jiangnan University (original Area of Wuxi Third People's Hospital), No. 585, North Xingyuan Road, Liang Xi District, Wuxi City 214000, Jiangsu Province, P. R. China.
Xia LiDepartment of Pharmacy, The Affiliated Hospital of Jiangnan University (original Area of Wuxi Third People's Hospital), No. 585, North Xingyuan Road, Liang Xi District, Wuxi City 214000, Jiangsu Province, P. R. China.
Wuxi Fourth People's Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Recent studies have identified photodynamic therapy (PDT) as a promising approach for cancer treatment. Here, in this study, we have constructed cancer cell membrane (CCM)-coated silica nanoparticles (SIL) as an artificial cell carrier (CCM/SIL) to effectively deliver chlorin e6 (Ce6), a commonly adopted photodynamic reagent (CCM/SIL/Ce6), to achieve enhanced PDT of cancer. In addition, apart from the generally recognized cytotoxicity induced by reactive oxygen species (ROS), our study also revealed that ROS could further potentiate the loss of intercellular junctions and integrity disruption as a result of down-regulation of VE-cadherin and CD31. Consequently, dendritic cells (DCs) were more readily accumulated to the tumor tissue and became maturated, which secreted tumor necrosis factor-α and interleukin-12 (IL-12) to trigger the following immune responses. Our work not only explored the anticancer feasibility of a new system but also demonstrated the underlining mechanisms responsible for PDT-induced anticancer effects, which offers a new perspective to employ and improve the efficacy of PDT and related systems.

Identifiers

PMID31460395
PMCPMC6682153
OpenAlexW2965182047

What OpenQuestion holds

Textmetadata
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.