Evidence map›Paper›PMID 28744329›Full record

ArticleTheranostics2017

PSMA-Targeted Theranostic Nanocarrier for Prostate Cancer.

Orielyz Flores, Santimukul Santra, Charalambos Kaittanis, Rania Bassiouni, Amr S Khaled, Annette R Khaled, Jan Grimm, J Manuel Perez

Open access · goldAbstract read
In one paragraph

Article in Theranostics, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed
4.1field-weighted citation impact, top 5% 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

35 citing papers in PubMed, 78 citations in OpenAlex.

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  14. The TRiCky Business of Protein Folding in Health and Disease.Frontiers in cell and developmental biology · 2022
    Review
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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

8 authors at 4 institutions in 1 country.

Orielyz FloresNanoscience Technology Center and Chemistry Department, University of Central Florida, Orlando FL, 32827.
Santimukul SantraNanoscience Technology Center and Chemistry Department, University of Central Florida, Orlando FL, 32827.
Charalambos KaittanisMolecular Pharmacology Program and Department of Radiology, Memorial Sloan Kettering Cancer Center, New York, NY, 10065.
Rania BassiouniBurnett School of Biomedical Science, College of Medicine, University of Central Florida, Orlando FL, 32827.
Amr S KhaledOrlando VA Medical Center, Orlando, FL 32827.
Annette R KhaledBurnett School of Biomedical Science, College of Medicine, University of Central Florida, Orlando FL, 32827.
Jan GrimmMolecular Pharmacology Program and Department of Radiology, Memorial Sloan Kettering Cancer Center, New York, NY, 10065.
J Manuel PerezBiomedical Imaging Research Institute, & Samuel Oschin Comprehensive Cancer Institute, Department of Biomedical Sciences and Department of Neurosurgery, Cedar Sinai Medical Center, Los Angeles CA, 90048.
University of Central Florida · USMemorial Sloan Kettering Cancer Center · USCedars-Sinai Medical Center · USOrlando VA Medical Center · US

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Nicholas D Socci · 1985 to 2026
$347.4M
Polymeric nanoparticles with imaging capability for therapeutic peptide deliveryR01EB019288 · NIBIB · UNIVERSITY OF CENTRAL FLORIDA · PI KHALED, ANNETTE R, PEREZ, J MANUEL · 2014 to 2017
$1.2M
NCI NIH HHS P30 CA008748NIBIB NIH HHS R01 EB019288
6 · The paper itself

Abstract

Herein, we report the use of a theranostic nanocarrier (Folate-HBPE(CT20p)) to deliver a therapeutic peptide to prostate cancer tumors that express PSMA (folate hydrolase 1). The therapeutic peptide (CT20p) targets and inhibits the chaperonin-containing TCP-1 (CCT) protein-folding complex, is selectively cytotoxic to cancer cells, and is non-toxic to normal tissue. With the delivery of CT20p to prostate cancer cells via PSMA, a dual level of cancer specificity is achieved: (1) selective targeting to PSMA-expressing prostate tumors, and (2) specific cytotoxicity to cancer cells with minimal toxicity to normal cells. The PSMA-targeting theranostic nanocarrier can image PSMA-expressing cells and tumors when a near infrared dye is used as cargo. Meanwhile, it can be used to treat PSMA-expressing tumors when a therapeutic, such as the CT20p peptide, is encapsulated within the nanocarrier. Even when these PSMA-targeting nanocarriers are taken up by macrophages, minimal cell death is observed in these cells, in contrast with doxorubicin-based therapeutics that result in significant macrophage death. Incubation of PSMA-expressing prostate cancer cells with the Folate-HBPE(CT20p) nanocarriers induces considerable changes in cell morphology, reduction in the levels of integrin β1, and lower cell adhesion, eventually resulting in cell death. These results are relevant as integrin β1 plays a key role in prostate cancer invasion and metastatic potential. In addition, the use of the developed PSMA-targeting nanocarrier facilitates the selective

Indexed as

AnimalsAntigens, SurfaceAntineoplastic AgentsCell Line, TumorCell SurvivalDisease Models, AnimalDrug CarriersGlutamate Carboxypeptidase IIHeterograftsHumansMaleMice, NudeMolecular Targeted TherapyNanoparticlesNeoplasm TransplantationPeptidesAntigens, SurfaceAntineoplastic AgentsDrug CarriersFOLH1 protein, humanGlutamate Carboxypeptidase IIPeptidespeptidepolymeric nanoparticlesprostate cancer.PSMA

Identifiers

PMID28744329
PMCPMC5525751
OpenAlexW2735627255

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.