Evidence map›Paper›PMID 27576789›Full record

ArticleScientific reports2016

Doxorubicin Conjugated to Immunomodulatory Anticancer Lactoferrin Displays Improved Cytotoxicity Overcoming Prostate Cancer Chemo resistance and Inhibits Tumour Development in TRAMP Mice.

Jayanth Suryanarayanan Shankaranarayanan, Jagat R Kanwar, Afrah Jalil Abd Al-Juhaishi, Rupinder K Kanwar

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 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
2.7field-weighted citation impact, top 11% 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

25 citing papers in PubMed, 54 citations in OpenAlex.

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  15. Bovine Lactoferrin Induces Cell Death in Human Prostate Cancer Cells.Oxidative medicine and cellular longevity · 2022
    Article
  16. Review
  17. Article
  18. Bioinspired particle engineering for non-invasive inhaled drug delivery to the lungs.Materials science & engineering. C, Materials for biological applications · 2021
    Article
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

4 authors at 1 institution in 1 country.

Jayanth Suryanarayanan ShankaranarayananNanomedicine-Laboratory of Immunology and Molecular Biomedical Research, School of Medicine, Faculty of Health, C-MMR, Deakin University, Geelong, Victoria 3216, Australia.
Jagat R KanwarNanomedicine-Laboratory of Immunology and Molecular Biomedical Research, School of Medicine, Faculty of Health, C-MMR, Deakin University, Geelong, Victoria 3216, Australia.
Afrah Jalil Abd Al-JuhaishiNanomedicine-Laboratory of Immunology and Molecular Biomedical Research, School of Medicine, Faculty of Health, C-MMR, Deakin University, Geelong, Victoria 3216, Australia.
Rupinder K KanwarNanomedicine-Laboratory of Immunology and Molecular Biomedical Research, School of Medicine, Faculty of Health, C-MMR, Deakin University, Geelong, Victoria 3216, Australia.
Deakin University · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Advanced, metastatic, castration resistant and chemo-resistant prostate cancer has triggered change in the drug development landscape against prostate cancer. Bovine lactoferrin (bLf) is currently attracting attention in clinics for its anti-cancer properties and proven safety profile. bLf internalises into cancer cells via receptor mediated endocytosis, boosts immunity and complements chemotherapy. We employed bLf as an excellent functional carrier protein for delivering doxorubicin (Dox) into DU145 cells, CD44+/EpCAM+ double positive enriched DU145 3D prostaspheres and drug resistant ADR1000-DU145 cells, thus circumventing Dox efflux, to overcome chemo-resistance. Successful bLf-Dox conjugation with iron free or iron saturated bLf forms did not affect the integrity and functionality of bLf and Dox. bLf-Dox internalised into DU145 cells within 6 h, enhanced nuclear Dox retention up to 24 h, and proved significantly effective (p < 0.001) in reducing LC50 value of Dox from 5.3 μM to 1.3 μM (4 fold). Orally fed iron saturated bLf-Dox inhibited tumour development, prolonged survival, reduced Dox induced general toxicity, cardiotoxicity, neurotoxicity in TRAMP mice and upregulated serum levels of anti-cancer molecules TNF-α, IFN-γ, CCL4 and CCL17. The study identifies promising potential of a novel and safer bLf-Dox conjugate containing a conventional cytotoxic drug along with bLf protein to target drug resistance.

Indexed as

AdenocarcinomaAnimalsApoptosisCattleCell Line, TumorChemokine CCL17Chemokine CCL4DoxorubicinDrug CarriersDrug Resistance, NeoplasmDrug Screening Assays, AntitumorDrug SynergismInterferon-gammaIronLactoferrinMaleCcl17 protein, mouseChemokine CCL17Chemokine CCL4DoxorubicinDrug CarriersInterferon-gammaIronLactoferrinNeoplasm ProteinsTopoisomerase II InhibitorsTumor Necrosis Factor-alpha

Identifiers

PMID27576789
PMCPMC5005995
OpenAlexW2507774775

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.