Evidence map›Paper›PMID 29019267›Full record

ArticleDrug delivery2017

GE11 peptide conjugated selenium nanoparticles for EGFR targeted oridonin delivery to achieve enhanced anticancer efficacy by inhibiting EGFR-mediated PI3K/AKT and Ras/Raf/MEK/ERK pathways.

Jiang Pi, Jinhuan Jiang, Huaihong Cai, Fen Yang, Hua Jin, Peihui Yang, Jiye Cai, Zheng W Chen

Open access · goldAbstract read
In one paragraph

Article in Drug delivery, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 41 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
41citing papers in PubMed, 1 pooled it
4.0field-weighted citation impact, top 5% 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, 1 synthesis or guideline pooled it, 98 citations in OpenAlex.

  1. COVID-19 and Selenium Deficiency: a Systematic Review.Biological trace element research · 2022
    Pooled it
  2. Review
  3. Review
  4. Co-adjuvant nano particles for hepatocellular carcinoma radiotherapy treatment.Journal of the Egyptian National Cancer Institute · 2025
    Article
  5. Review
  6. Review
  7. Review
  8. Review
  9. Review
  10. Article
  11. Article
  12. Article
  13. Biological evaluation of extracellular mycosynthesized silver nanoparticles by Trichoderma asperellum.Biometals : an international journal on the role of metal ions in biology, biochemistry, and medicine · 2023
    Article
  14. Review
  15. Review
  16. Nanodrugs systems for therapy and diagnosis of esophageal cancer.Frontiers in bioengineering and biotechnology · 2023
    Review
  17. EGFR-targeted pemetrexed therapy of malignant pleural mesothelioma.Drug delivery and translational research · 2022
    Article
  18. Review
  19. Review
  20. Antiviral potential of nanoparticles for the treatment of Coronavirus infections.Journal of trace elements in medicine and biology : organ of the Society for Minerals and Trace Elements (GMS) · 2022
    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

8 authors at 3 institutions in 3 countries.

Jiang Pia State Key Laboratory of Quality Research in Chinese Medicines , Macau University of Science and Technology , Macau , PR China.
Jinhuan Jianga State Key Laboratory of Quality Research in Chinese Medicines , Macau University of Science and Technology , Macau , PR China.
Huaihong Caic Department of Chemistry , Jinan University , Guangzhou , PR China.
Fen Yanga State Key Laboratory of Quality Research in Chinese Medicines , Macau University of Science and Technology , Macau , PR China.
Hua Jina State Key Laboratory of Quality Research in Chinese Medicines , Macau University of Science and Technology , Macau , PR China.
Peihui Yangc Department of Chemistry , Jinan University , Guangzhou , PR China.
Jiye Caia State Key Laboratory of Quality Research in Chinese Medicines , Macau University of Science and Technology , Macau , PR China.
Zheng W Chenb Department of Microbiology and Immunology , University of Illinois at Chicago , Chicago , IL , USA.
Macau University of Science and Technology · MOJinan University · CNUniversity of Illinois Chicago · US

Funding

MODEL OF AIDS VIRUS-RELATED PULMONARY TUBERCULOSISR01HL064560 · NHLBI · UNIVERSITY OF ILLINOIS AT CHICAGO · PI CHEN, ZHENG W · 1999 to 2014
$9.5M
Ag-specific gamma delta T cells and immunity to TB/AIDS-related TBR01OD015092 · OD · UNIVERSITY OF ILLINOIS AT CHICAGO · PI CHEN, ZHENG W · 2013 to 2017
$3.0M
Anti-TB sterilizing immunity in immune and HIV+ individualsR01HL129887 · NHLBI · UNIVERSITY OF ILLINOIS AT CHICAGO · PI CHEN, ZHENG W · 2015 to 2018
$2.1M
Immune function and mechanism of Tim3 expression and Tim3+ T cells in TB & HIV+TBR01AI106590 · NIAID · UNIVERSITY OF ILLINOIS AT CHICAGO · PI CHEN, ZHENG W · 2013 to 2015
$600k
NHLBI NIH HHS R01 HL064560NHLBI NIH HHS R01 HL129887NIAID NIH HHS R01 AI106590NIH HHS R01 OD015092
6 · The paper itself

Abstract

Selenium nanoparticles (Se NPs) have attracted increasing interest in recent decades because of their anticancer, immunoregulation, and drug carrier functions. In this study, GE11 peptide-conjugated Se NPs (GE11-Se NPs), a nanosystem targeting EGFR over-expressed cancer cells, were synthesized for oridonin delivery to achieve enhanced anticancer efficacy. Oridonin loaded and GE11 peptide conjugated Se NPs (GE11-Ori-Se NPs) were found to show enhanced cellular uptake in cancer cells, which resulted in enhanced cancer inhibition against cancer cells and reduced toxicity against normal cells. After accumulation into the lysosomes of cancer cells and increase of oridonin release under acid condition, GE11-Ori-Se NPs were further transported into cytoplasm after the damage of lysosomal membrane integrity. GE11-Ori-Se NPs were found to induce cancer cell apoptosis by inducting reactive oxygen species (ROS) production, activating mitochondria-dependent pathway, inhibiting EGFR-mediated PI3K/AKT and inhibiting Ras/Raf/MEK/ERK pathways. GE11-Se NPs were also found to show active targeting effects against the tumor tissue in esophageal cancer bearing mice. And in nude mice xenograft model, GE11-Ori-Se NPs significantly inhibited the tumor growth via inhibition of tumor angiogenesis by reducing the angiogenesis-marker CD31 and activation of the immune system by enhancing IL-2 and TNF-α production. The selenium contents in mice were found to accumulate into liver, tumor, and kidney, but showed no significant toxicity against liver and kidney. This cancer-targeted design of Se NPs provides a new strategy for synergistic treating of cancer with higher efficacy and reduced side effects, introducing GE11-Ori-Se NPs as a candidate for further evaluation as a chemotherapeutic agent for EGFR over-expressed esophageal cancers.

Indexed as

AnimalsAntineoplastic AgentsApoptosisCell Line, TumorDiterpenes, KauraneDrug CarriersDrug LiberationErbB ReceptorsHumansInterleukin-2MAP Kinase Signaling SystemMiceNanoparticlesPeptidesPlatelet Endothelial Cell Adhesion Molecule-1Reactive Oxygen SpeciesAntineoplastic AgentsDiterpenes, KauraneDrug CarriersErbB ReceptorsGE11 peptideInterleukin-2oridoninPeptidesPlatelet Endothelial Cell Adhesion Molecule-1Reactive Oxygen SpeciesSeleniumTumor Necrosis Factor-alphadeliveryEGFR targetingGE11 peptideoridoninSelenium nanoparticles

Identifiers

PMID29019267
PMCPMC6920706
OpenAlexW2761074492

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.