Evidence map›Paper›PMID 27081693›Full record

ArticleOncotarget2016

Efficient therapeutic delivery by a novel cell-permeant peptide derived from KDM4A protein for antitumor and antifibrosis.

Hu Wang, Jie-Lan Ma, Ying-Gui Yang, Yang Song, Jiao Wu, Yan-Yan Qin, Xue-Li Zhao, Jun Wang, Li-Li Zou, Jiang-Feng Wu and 2 more

Abstract read
In one paragraph

Article in Oncotarget, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing 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

17 citing papers in PubMed.

  1. Recombinant RGD-Apoptins Decrease Human Melanoma Cell Viability.International journal of molecular sciences · 2025
    Article
  2. Review
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  4. Review
  5. Article
  6. Review
  7. Article
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  10. Drug delivery · 2021
    Article
  11. Article
  12. Article
  13. Article
  14. Review
  15. Review
  16. AMolecules (Basel, Switzerland) · 2018
    Article
  17. Article
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.

Hu WangThe Institute of Cell Therapy, China Three Gorges University, Yichang 443002, China.
Jie-Lan MaMedical School, China Three Gorges University, Yichang 443002, China.
Ying-Gui YangThe Institute of Cell Therapy, China Three Gorges University, Yichang 443002, China.
Yang SongThe Institute of Cell Therapy, China Three Gorges University, Yichang 443002, China.
Jiao WuThe Institute of Cell Therapy, China Three Gorges University, Yichang 443002, China.
Yan-Yan QinMedical School, China Three Gorges University, Yichang 443002, China.
Xue-Li ZhaoMedical School, China Three Gorges University, Yichang 443002, China.
Jun WangThe Institute of Cell Therapy, China Three Gorges University, Yichang 443002, China.
Li-Li ZouThe Institute of Cell Therapy, China Three Gorges University, Yichang 443002, China.
Jiang-Feng WuThe Institute of Cell Therapy, China Three Gorges University, Yichang 443002, China.
Jun-Ming LiThe Institute of Cell Therapy, China Three Gorges University, Yichang 443002, China.
Chang-Bai LiuThe Institute of Cell Therapy, China Three Gorges University, Yichang 443002, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cell-penetrating peptide (CPP) based delivery have provided immense potential for the therapeutic applications, however, most of nonhuman originated CPPs carry the risk of possible cytotoxicity and immunogenicity, thus may restricting to be used. Here, we describe a novel human-derived CPP, denoted hPP10, and hPP10 has cell-penetrating properties evaluated by CellPPD web server, as well as In-Vitro and In-Vivo analysis. In vitro studies showed that hPP10-FITC was able to penetrate into various cells including primary cultured cells, likely through an endocytosis pathway. And functionalized macromolecules, such as green fluorescent protein (GFP), tumor-specific apoptosis inducer Apoptin as well as biological active enzyme GCLC (Glutamate-cysteine ligase, catalytic subunit) can be delivered by hPP10 in vitro and in vivo. Collectively, our results suggest that hPP10 provide a novel and versatile tool to deliver exogenous proteins or drugs for clinical applications as well as reprogrammed cell-based therapy.

Indexed as

A549 CellsAnimalsAntineoplastic AgentsApoptosisCell Line, TumorCell MembraneCell-Penetrating PeptidesDrug Delivery SystemsEndocytosisFibrosisGreen Fluorescent ProteinsHeLa CellsHep G2 CellsHumansJumonji Domain-Containing Histone DemethylasesMacromolecular SubstancesAntineoplastic AgentsCell-Penetrating PeptidesGreen Fluorescent ProteinsJumonji Domain-Containing Histone DemethylasesKDM4A protein, humanMacromolecular SubstancesPeptidesanti-tumorcell-penetrating peptides (CPPs)GFPinternalizationmelanoma

Identifiers

PMID27081693
PMCPMC5226491

What OpenQuestion holds

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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.