Evidence map›Paper›PMID 27725731›Full record

ArticleScientific reports2016

Combinatorial nanocarrier based drug delivery approach for amalgamation of anti-tumor agents in breast cancer cells: an improved nanomedicine strategy.

Chandran Murugan, Kathirvel Rayappan, Ramar Thangam, Ramasamy Bhanumathi, Krishnamurthy Shanthi, Raju Vivek, Ramasamy Thirumurugan, Atanu Bhattacharyya, Srinivasan Sivasubramanian, Palani Gunasekaran and 1 more

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in Scientific reports, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 41 papers.

0numbers the graph read from it
0cells of the map it votes in
41citing papers in PubMed
8.4field-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

41 citing papers in PubMed, 138 citations in OpenAlex.

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  16. Date Palm Extract (Plants (Basel, Switzerland) · 2021
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

11 authors at 6 institutions in 2 countries.

Chandran MuruganProteomics and Molecular Cell Physiology Laboratory, Department of Zoology, Periyar University, Salem-636011, TamilNadu, INDIA.
Kathirvel RayappanProteomics and Molecular Cell Physiology Laboratory, Department of Zoology, Periyar University, Salem-636011, TamilNadu, INDIA.
Ramar ThangamKing Institute of Preventive Medicine &Research, Guindy, Chennai 600 032, Tamil Nadu, INDIA.
Ramasamy BhanumathiProteomics and Molecular Cell Physiology Laboratory, Department of Zoology, Periyar University, Salem-636011, TamilNadu, INDIA.
Krishnamurthy ShanthiDepartment of Zoology, Bharathiar University, Coimbatore, 641 046, Tamil Nadu, INDIA.
Raju VivekDepartment of Biomedical Engineering, Shanghai Jiao Tong University, Shanghai, 200 240, CHINA.
Ramasamy ThirumuruganDepartment of Animal Science, Bharathidasan University, Tiruchirappalli, 620 024, Tamil Nadu, INDIA.
Atanu BhattacharyyaNanotechnology Section, Department of Biomedical Engineering, Rajiv Gandhi Institute of Technology and Research Centre, Hebbal, Bangalore, 560 032, Karnataka, INDIA.
Srinivasan SivasubramanianKing Institute of Preventive Medicine &Research, Guindy, Chennai 600 032, Tamil Nadu, INDIA.
Palani GunasekaranKing Institute of Preventive Medicine &Research, Guindy, Chennai 600 032, Tamil Nadu, INDIA.
Soundarapandian KannanProteomics and Molecular Cell Physiology Laboratory, Department of Zoology, Periyar University, Salem-636011, TamilNadu, INDIA.
Periyar University · INKing Institute of Preventive Medicine and Research · INBharathiar University · INBharathidasan University · INRajiv Gandhi University of Health Sciences · INShanghai Jiao Tong University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Combination therapy of multiple drugs through a single system is exhibiting high therapeutic effects. We investigate nanocarrier mediated inhibitory effects of topotecan (TPT) and quercetin (QT) on triple negative breast cancer (TNBC) (MDA-MB-231) and multi drug resistant (MDR) type breast cancer cells (MCF-7) with respect to cellular uptake efficiency and therapeutic mechanisms as in vitro and in vivo. The synthesized mesoporous silica nanoparticle (MSN) pores used for loading TPT; the outer of the nanoparticles was decorated with poly (acrylic acid) (PAA)-Chitosan (CS) as anionic inner-cationic outer layer respectively and conjugated with QT. Subsequently, grafting of arginine-glycine-aspartic acid (cRGD) peptide on the surface of nanocarrier (CPMSN) thwarted the uptake by normal cells, but facilitated their uptake in cancer cells through integrin receptor mediated endocytosis and the dissociation of nanocarriers due to the ability to degrade of CS and PAA in acidic pH, which enhance the intracellular release of drugs. Subsequently, the released drugs induce remarkable molecular activation as well as structural changes in tumor cell endoplasmic reticulum, nucleus and mitochondria that can trigger cell death. The valuable CPMSNs may open up new avenues in developing targeted therapeutic strategies to treat cancer through serving as an effective drug delivery podium.

Indexed as

Antineoplastic Combined Chemotherapy ProtocolsDrug CarriersAcrylic ResinsChitosanDrug Resistance, MultipleDrug Resistance, NeoplasmFemaleHumansMCF-7 CellsNanoparticlesOligopeptidesQuercetinSilicon DioxideTopotecanTriple Negative Breast NeoplasmsAcrylic Resinsarginyl-glycyl-aspartic acidcarbopol 940ChitosanDrug CarriersOligopeptidesQuercetinSilicon DioxideTopotecan

Identifiers

PMID27725731
PMCPMC5057072
OpenAlexW2530228098

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.