Evidence map›Paper›PMID 22802668›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2012

Laminin receptor specific therapeutic gold nanoparticles (198AuNP-EGCg) show efficacy in treating prostate cancer.

Ravi Shukla, Nripen Chanda, Ajit Zambre, Anandhi Upendran, Kavita Katti, Rajesh R Kulkarni, Satish Kumar Nune, Stan W Casteel, Charles Jeffrey Smith, Jatin Vimal and 11 more

Open access · bronzeAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 98 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
98citing papers in PubMed, 1 pooled it
13.7field-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

98 citing papers in PubMed, 1 synthesis or guideline pooled it, 265 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Review
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  14. Brachytherapy at the nanoscale with protein functionalized and intrinsically radiolabeled [European journal of nuclear medicine and molecular imaging · 2024
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  15. Molecules (Basel, Switzerland) · 2024
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  16. Article
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  19. Nano-Ayurvedic Medicine Approaches UsingNanotechnology, science and applications · 2024
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  20. Review

38 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

21 authors at 4 institutions in 2 countries.

Ravi ShuklaDepartment of Radiology, Harry S Truman Veterans Administration Medical Center, and Missouri University Research Reactor, University of Missouri, Columbia, MO 65212, USA.
Nripen Chanda
Ajit Zambre
Anandhi Upendran
Kavita Katti
Rajesh R Kulkarni
Satish Kumar Nune
Stan W Casteel
Charles Jeffrey Smith
Jatin Vimal
Evan Boote
J David Robertson
Para Kan
Hendrik Engelbrecht
Lisa D Watkinson
Terry L Carmack
John R Lever
Cathy S Cutler
Charles Caldwell
Raghuraman Kannan
Kattesh V Katti
University of Missouri · USDivision of Chemistry · USNanoparticle BioChem (United States) · USInstitute for Nuclear Science and Technology · VN

Funding

Hybrid Nanoparticles in Imaging and Therapy of Prostate*R01CA119412 · NCI · UNIVERSITY OF MISSOURI-COLUMBIA · PI KATTI, KATTESH V · 2005 to 2009
$3.1M
NCI NIH HHS 5R01CA119412-01NCI NIH HHS NIH-1R21CA182460-01NCI NIH HHS R01 CA119412
6 · The paper itself

Abstract

Systemic delivery of therapeutic agents to solid tumors is hindered by vascular and interstitial barriers. We hypothesized that prostate tumor specific epigallocatechin-gallate (EGCg) functionalized radioactive gold nanoparticles, when delivered intratumorally (IT), would circumvent transport barriers, resulting in targeted delivery of therapeutic payloads. The results described herein support our hypothesis. We report the development of inherently therapeutic gold nanoparticles derived from the Au-198 isotope; the range of the (198)Au β-particle (approximately 11 mm in tissue or approximately 1100 cell diameters) is sufficiently long to provide cross-fire effects of a radiation dose delivered to cells within the prostate gland and short enough to minimize the radiation dose to critical tissues near the periphery of the capsule. The formulation of biocompatible (198)AuNPs utilizes the redox chemistry of prostate tumor specific phytochemical EGCg as it converts gold salt into gold nanoparticles and also selectively binds with excellent affinity to Laminin67R receptors, which are over expressed in prostate tumor cells. Pharmacokinetic studies in PC-3 xenograft SCID mice showed approximately 72% retention of (198)AuNP-EGCg in tumors 24 h after intratumoral administration. Therapeutic studies showed 80% reduction of tumor volumes after 28 d demonstrating significant inhibition of tumor growth compared to controls. This innovative nanotechnological approach serves as a basis for designing biocompatible target specific antineoplastic agents. This novel intratumorally injectable (198)AuNP-EGCg nanotherapeutic agent may provide significant advances in oncology for use as an effective treatment for prostate and other solid tumors.

Indexed as

Metal NanoparticlesAnimalsAnticarcinogenic AgentsCatechinCell Line, TumorFemaleGoldGold RadioisotopesHumansMaleMiceMice, SCIDParticle SizeProstatic NeoplasmsXenograft Model Antitumor AssaysAnticarcinogenic AgentsCatechinepigallocatechin gallateGoldGold Radioisotopes

Identifiers

PMID22802668
PMCPMC3411993
OpenAlexW1984092714

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.