Evidence map›Paper›PMID 37294758›Full record

ArticleScience advances2023

Autonomous metal-organic framework nanorobots for active mitochondria-targeted cancer therapy.

Xiqi Peng, Songsong Tang, Daitian Tang, Dewang Zhou, Yangyang Li, Qiwei Chen, Fangchen Wan, Heather Lukas, Hong Han, Xueji Zhang and 2 more

Open access · goldAbstract read
In one paragraph

Article in Science advances, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 43 papers.

0numbers the graph read from it
0cells of the map it votes in
43citing papers in PubMed
16.7field-weighted citation impact, top 1% 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

43 citing papers in PubMed, 89 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

12 authors at 4 institutions in 2 countries.

Xiqi PengLuohu Clinical Institute of Shantou University Medical College, Shantou University Medical College, Shantou 515000, P. R. China.ORCID 0000-0003-4421-5188
Songsong TangInstitute of Urology, The Third Affiliated Hospital of Shenzhen University, Shenzhen 518000, P. R. China.ORCID 0000-0003-4699-6563
Daitian TangLuohu Clinical Institute of Shantou University Medical College, Shantou University Medical College, Shantou 515000, P. R. China.
Dewang ZhouInstitute of Urology, The Third Affiliated Hospital of Shenzhen University, Shenzhen 518000, P. R. China.
Yangyang LiInstitute of Urology, The Third Affiliated Hospital of Shenzhen University, Shenzhen 518000, P. R. China.ORCID 0000-0002-7443-7286
Qiwei ChenLuohu Clinical Institute of Shantou University Medical College, Shantou University Medical College, Shantou 515000, P. R. China.
Fangchen WanInstitute of Urology, The Third Affiliated Hospital of Shenzhen University, Shenzhen 518000, P. R. China.
Heather LukasAndrew and Peggy Cherng Department of Medical Engineering, California Institute of Technology, Pasadena, CA 91125, USA.ORCID 0000-0002-8160-9066
Hong HanAndrew and Peggy Cherng Department of Medical Engineering, California Institute of Technology, Pasadena, CA 91125, USA.ORCID 0000-0002-2852-8662
Xueji ZhangSchool of Biomedical Engineering, Health Science Centre, Shenzhen University, Shenzhen 518060, P. R. China.ORCID 0000-0002-0035-3821
Wei GaoAndrew and Peggy Cherng Department of Medical Engineering, California Institute of Technology, Pasadena, CA 91125, USA.ORCID 0000-0002-8503-4562
Song WuLuohu Clinical Institute of Shantou University Medical College, Shantou University Medical College, Shantou 515000, P. R. China.ORCID 0000-0003-3504-1630
California Institute of Technology · USShantou University · CNShenzhen Third People’s Hospital · CNShenzhen University Health Science Center · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Nanorobotic manipulation to access subcellular organelles remains unmet due to the challenge in achieving intracellular controlled propulsion. Intracellular organelles, such as mitochondria, are an emerging therapeutic target with selective targeting and curative efficacy. We report an autonomous nanorobot capable of active mitochondria-targeted drug delivery, prepared by facilely encapsulating mitochondriotropic doxorubicin-triphenylphosphonium (DOX-TPP) inside zeolitic imidazolate framework-67 (ZIF-67) nanoparticles. The catalytic ZIF-67 body can decompose bioavailable hydrogen peroxide overexpressed inside tumor cells to generate effective intracellular mitochondriotropic movement in the presence of TPP cation. This nanorobot-enhanced targeted drug delivery induces mitochondria-mediated apoptosis and mitochondrial dysregulation to improve the in vitro anticancer effect and suppression of cancer cell metastasis, further verified by in vivo evaluations in the subcutaneous tumor model and orthotopic breast tumor model. This nanorobot unlocks a fresh field of nanorobot operation with intracellular organelle access, thereby introducing the next generation of robotic medical devices with organelle-level resolution for precision therapy.

Indexed as

Metal-Organic FrameworksNanoparticlesNeoplasmsDoxorubicinDrug CarriersDrug Delivery SystemsHumansMitochondriaDoxorubicinDrug CarriersMetal-Organic Frameworks

Identifiers

PMID37294758
PMCPMC10256165
OpenAlexW4379983767

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.