Evidence map›Paper›PMID 39438495›Full record

ArticleScientific reports2024

Alginate-modified graphene oxide anchored with lactoperoxidase as a novel bioactive nanocombination for colorectal cancer therapy.

AbdElAziz A Nayl, Esmail M El-Fakharany, Ahmed I Abd-Elhamid, Wael A A Arafa, Ahmed H Alanazi, Ismail M Ahmed, Mohamed A Abdelgawad, Ashraf A Aly, Stefan Bräse

Abstract read
In one paragraph

Article in Scientific reports, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
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

1 citing paper in PubMed.

  1. Review
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

9 authors.

AbdElAziz A NaylDepartment of Chemistry, College of Science, Jouf University, Sakaka, Aljouf, 72341, Saudi Arabia. aanayel@ju.edu.sa.
Esmail M El-FakharanyProtein Research Department, Genetic Engineering and Biotechnology Research Institute GEBRI, City of Scientific Research and Technological Applications (SRTA city), New Borg El-Arab, Alexandria, 21934, Egypt.
Ahmed I Abd-ElhamidComposites and Nanostructured Materials Research Department, Advanced Technology and New Materials Research Institute, City of Scientific Research and Technological Applications (SRTA-City), New Borg Al-Arab, Alexandria, 21934, Egypt.
Wael A A ArafaDepartment of Chemistry, College of Science, Jouf University, Sakaka, Aljouf, 72341, Saudi Arabia.
Ahmed H AlanaziDepartment of Chemistry, College of Science, Jouf University, Sakaka, Aljouf, 72341, Saudi Arabia.
Ismail M AhmedDepartment of Chemistry, College of Science, Jouf University, Sakaka, Aljouf, 72341, Saudi Arabia.
Mohamed A AbdelgawadDepartment of Pharmaceutical Chemistry, College of Pharmacy, Jouf University, Sakaka, 72341, Al Jouf, Saudi Arabia.
Ashraf A AlyChemistry Department, Faculty of Science, Organic Division, Minia University, El-Minia, 61519, Egypt.
Stefan BräseInstitute of Biological and Chemical Systems - Functional Molecular Systems (IBCS-FMS), Kaiserstrasse 12, Karlsruhe, 76131, Germany. stefan.braese@kit.edu.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

It is imperative to explore new biocompatible drugs with low toxicity for use in medicinal fields such as fighting tumors. Bovine lactoperoxidase (BLPO) stems from the most important enzymes in the bovine whey that provide a proper pattern for nano-formulation with nanomaterials. LPO is a suitable protein to be coated or adsorbed to alginate modified graphene oxide (GO-SA), which forms the modified GO-SA-LPO hybrid structure. This novel combination provides LPO stability with strong anticancer effects and boosts immunity response. The characterization results obtained from different techniques confirmed a successful LPO adsorption on the GO-SA composite surface. Moreover, nano-formulation of LPO with GO-SA composite exhibited a reduction in its size and overall charge. In addition, the experimental results showed greater LPO activity stability in the modified GO-SA-LPO nanocombination than free LPO after storage for 10 weeks at 4 °C. The in vitro study, a crucial step in the validation of our approach, demonstrated that the modified GO-SA-LPO nanocombination showed a potent anticancer selectivity toward colon cancer cell lines more than GO-SA composite or free form of LPO, which enhanced in a dose-dependent manner with high safety manner against normal cells. The apoptotic effect of this novel nanocombination was confirmed by the greatest variations in the expression of both well-known apoptosis genes (p53 and Bcl-2), severe changes in the cellular morphology, DNA fragmentation, and nuclear staining with fluorescence yellow and orange of the target cancer cells. Also, this superior efficacy of the modified GO-SA-LPO nanocombination was induced by suppressing some pro-inflammatory cytokines, including tumor necrosis factor-alpha (TNF-α), interleukin (IL-6), and necrosis factor-kappa B (NF-ĸB). Our observations presented that the modified nanocombination of LPO may offer a novel remedy for treating colon tumors via induced apoptosis pathway, inflammation reduction, and immune response improvement.

Indexed as

AlginatesColorectal NeoplasmsGraphiteLactoperoxidaseAnimalsAntineoplastic AgentsApoptosisCattleCell Line, TumorHumansAlginatesAntineoplastic Agentsgraphene oxideGraphiteLactoperoxidaseAlginateAnti-cancer and apoptosisBiocompatible drugsGraphene oxide nanocompositeLactoperoxidase nanocombination

Identifiers

PMID39438495
PMCPMC11496692

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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.