Evidence map›Paper›PMID 25028336›Full record

ArticleBiomaterials2014

Anti-cancer activity of curcumin loaded nanoparticles in prostate cancer.

Murali M Yallapu, Sheema Khan, Diane M Maher, Mara C Ebeling, Vasudha Sundram, Neeraj Chauhan, Aditya Ganju, Swathi Balakrishna, Brij K Gupta, Nadeem Zafar and 2 more

Open access · greenAbstract read
In one paragraph

Article in Biomaterials, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 97 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
97citing papers in PubMed, 2 pooled it
9.4field-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

97 citing papers in PubMed, 2 syntheses or guidelines pooled it, 284 citations in OpenAlex.

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  15. Curcumin's Radioprotective Effects on Zebrafish Embryos.Antioxidants (Basel, Switzerland) · 2024
    Article
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37 more citing papers are in PubMed but not listed here.

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 2 institutions in 1 country.

Murali M YallapuDepartment of Pharmaceutical Sciences and The Center for Cancer Research, College of Pharmacy, University of Tennessee Health Science Center, Memphis, TN 38163, USA.
Sheema KhanDepartment of Pharmaceutical Sciences and The Center for Cancer Research, College of Pharmacy, University of Tennessee Health Science Center, Memphis, TN 38163, USA.
Diane M MaherCancer Biology Research Center, Sanford Research, Sioux Falls, SD 57104, USA.
Mara C EbelingCancer Biology Research Center, Sanford Research, Sioux Falls, SD 57104, USA.
Vasudha SundramCancer Biology Research Center, Sanford Research, Sioux Falls, SD 57104, USA.
Neeraj ChauhanDepartment of Pharmaceutical Sciences and The Center for Cancer Research, College of Pharmacy, University of Tennessee Health Science Center, Memphis, TN 38163, USA.
Aditya GanjuDepartment of Pharmaceutical Sciences and The Center for Cancer Research, College of Pharmacy, University of Tennessee Health Science Center, Memphis, TN 38163, USA.
Swathi BalakrishnaDepartment of Pharmaceutical Sciences and The Center for Cancer Research, College of Pharmacy, University of Tennessee Health Science Center, Memphis, TN 38163, USA.
Brij K GuptaCancer Biology Research Center, Sanford Research, Sioux Falls, SD 57104, USA.
Nadeem ZafarDepartment of Pathology, College of Medicine, University of Tennessee Health Science Center, Memphis, TN 38163, USA.
Meena JaggiDepartment of Pharmaceutical Sciences and The Center for Cancer Research, College of Pharmacy, University of Tennessee Health Science Center, Memphis, TN 38163, USA.
Subhash C ChauhanDepartment of Pharmaceutical Sciences and The Center for Cancer Research, College of Pharmacy, University of Tennessee Health Science Center, Memphis, TN 38163, USA. Electronic address: schauha1@uthsc.edu.
University of Tennessee Health Science Center · USSanford Research · US

Funding

The Impact of PD-1 Inhibition on Immune-Response to ChemoradiotherapyP20GM103548 · NIGMS · SANFORD RESEARCH/USD · PI MISKIMINS, W KEITH · 2012 to 2020
$20.8M
Etiology of cervical cancer health disparity in American Indian womenU01CA162106 · NCI · UNIVERSITY OF TENNESSEE HEALTH SCI CTR · PI CHAUHAN, SUBHASH C., JAGGI, MEENA · 2012 to 2016
$1.5M
Aspects of MUC13 Mucin in CancerR01CA142736 · NCI · UNIVERSITY OF TENNESSEE HEALTH SCI CTR · PI CHAUHAN, SUBHASH C. · 2010 to 2013
$1.2M
NCI NIH HHS R01 CA142736NCI NIH HHS U01 CA162106NIGMS NIH HHS P20 GM103548NIGMS NIH HHS P20 GM103548-02
6 · The paper itself

Abstract

Prostate cancer is the most commonly diagnosed cancer disease in men in the Unites States and its management remains a challenge in everyday oncology practice. Thus, advanced therapeutic strategies are required to treat prostate cancer patients. Curcumin (CUR) is a promising anticancer agent for various cancer types. The objective of this study was to evaluate therapeutic potential of novel poly(lactic-co-glycolic acid)- CUR nanoparticles (PLGA-CUR NPs) for prostate cancer treatment. Our results indicate that PLGA-CUR NPs efficiently internalize in prostate cancer cells and release biologically active CUR in cytosolic compartment of cells for effective therapeutic activity. Cell proliferation (MTS), clonogenic, and Western blot analyses reveal that PLGA-CUR NPs can effectively inhibit proliferation and colony formation ability of prostate cancer cells than free CUR. PLGA-CUR NPs showed superior tumor regression compared to CUR in xenograft mice. Further investigations reveal that PLGA-CUR NPs inhibit nuclear β-catenin and AR expression in cells and in tumor xenograft tissues. It also suppresses STAT3 and AKT phosphorylation and leads to apoptosis via inhibition of key anti-apoptotic proteins, Mcl-1, Bcl-xL and caused induction of PARP cleavage. Additionally, significant downregulation of oncogenic miR21 and up-regulation of miR-205 was observed with PLGA-CUR NPs treatment as determined by RT-PCR and in situ hybridization analyses. A superior anti-cancer potential was attained with PSMA antibody conjugated PLGA-CUR NPs in prostate cancer cells and a significant tumor targeting of (131)I labeled PSMA antibody was achieved with PLGA-CUR NPs in prostate cancer xenograft mice model. In conclusion, PLGA-CUR NPs can significantly accumulate and exhibit superior anticancer activity in prostate cancer.

Indexed as

AnimalsAntineoplastic AgentsApoptosisbeta CateninCell Line, TumorCell ProliferationCurcuminEndocytosisHumansMaleMice, NudeMicroRNAsNanoparticlesProstate-Specific AntigenProstatic NeoplasmsReceptors, AndrogenAntineoplastic Agentsbeta CateninCurcuminMicroRNAsProstate-Specific AntigenReceptors, AndrogenChemopreventionCurcuminNanoparticlesProstate cancerTargeted delivery

Identifiers

PMID25028336
PMCPMC4220612
OpenAlexW1988943017

What OpenQuestion holds

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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.