Evidence map›Paper›PMID 35228516›Full record

ArticleSignal transduction and targeted therapy2022

Asymmetric, amphiphilic RGD conjugated phthalocyanine for targeted photodynamic therapy of triple negative breast cancer.

Rui Li, Yiming Zhou, Yijia Liu, Xingpeng Jiang, Wenlong Zeng, Zhuoran Gong, Gang Zheng, Desheng Sun, Zhifei Dai

Open access · goldAbstract read
In one paragraph

Article in Signal transduction and targeted therapy, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
7.1field-weighted citation impact, top 2% 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

17 citing papers in PubMed, 50 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

9 authors at 3 institutions in 2 countries.

Rui Li *Department of Biomedical Engineering, College of Future Technology, National Biomedical Imaging Center, Peking University, Beijing, 100871, China.
Yiming Zhou *Department of Biomedical Engineering, College of Future Technology, National Biomedical Imaging Center, Peking University, Beijing, 100871, China.
Yijia LiuDepartment of Biomedical Engineering, College of Future Technology, National Biomedical Imaging Center, Peking University, Beijing, 100871, China.
Xingpeng JiangDepartment of Biomedical Engineering, College of Future Technology, National Biomedical Imaging Center, Peking University, Beijing, 100871, China.
Wenlong ZengDepartment of Biomedical Engineering, College of Future Technology, National Biomedical Imaging Center, Peking University, Beijing, 100871, China.
Zhuoran GongDepartment of Biomedical Engineering, College of Future Technology, National Biomedical Imaging Center, Peking University, Beijing, 100871, China.
Gang ZhengPrincess Margaret Cancer Centre, University Health Network, 101 College Street, PMCRT 5-354, Toronto, Ontario, M5G 1L7, Canada.
Desheng SunDepartment of Ultrasonic Imaging, Peking University Shenzhen Hospital, Shenzhen, China. szdssun@163.com.
Zhifei DaiDepartment of Biomedical Engineering, College of Future Technology, National Biomedical Imaging Center, Peking University, Beijing, 100871, China. zhifei.dai@pku.edu.cn.
Peking University · CNPeking University Shenzhen Hospital · CNPrincess Margaret Cancer Centre · CA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Targeted photodynamic therapy (TPDT) is considered superior to conventional photodynamic therapy due to the enhanced uptake of photosensitizers by tumor cells. In this paper, an amphiphilic and asymmetric cyclo-Arg-Gly-Asp-d-Tyr-Lys(cRGDyK)-conjugated silicon phthalocyanine (RSP) was synthesized by covalently attaching the tripeptide Arg-Gly-Asp (RGD) to silicone phthalocyanine in the axial direction for TPDT of triple-negative breast cancer (TNBC). RSP was characterized by spectroscopy as a monomer in physiological buffer. Meanwhile, the modification of RSP with RGD led to a high accumulation of the photosensitizer in TNBC cells overexpressing ανβ3 integrin receptors which can bind RGD, greatly reducing the risk of phototoxicity. In vitro photodynamic experiments showed that the IC50 of RSP was 295.96 nM in the 4T1 cell line, which caused significant apoptosis of the tumor cells. The tumor inhibition rate of RSP on the orthotopic murine TNBC achieved 74%, while the untargeted photosensitizer exhibited no obvious tumor inhibition. Overall, such novel targeted silicon phthalocyanine has good potential for clinical translation due to its simple synthesis route, strong targeting, and high therapeutic efficacy for TPDT treatment of TNBC.

Indexed as

PhotochemotherapyTriple Negative Breast NeoplasmsAnimalsCell Line, TumorHumansIsoindolesMiceOligopeptidesarginyl-glycyl-aspartic acidIsoindolesOligopeptidesphthalocyanine

Identifiers

PMID35228516
PMCPMC8885659
OpenAlexW4214633714

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.