Evidence map›Paper›PMID 30790141›Full record

ArticleJournal of cardiovascular translational research2019

KC21 Peptide Inhibits Angiogenesis and Attenuates Hypoxia-Induced Retinopathy.

Chi-Sheng Lu, Yi-Nan Lee, Shin-Wei Wang, Yih-Jer Wu, Cheng-Huang Su, Chin-Ling Hsieh, Ting Yi Tien, Bo-Jeng Wang, Min-Che Chen, Chun-Wei Chen and 1 more

Open access · hybridAbstract readComparative Study
In one paragraph

Article in Journal of cardiovascular translational research, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.2field-weighted citation impact, top 49% 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

3 citing papers in PubMed, 3 citations in OpenAlex.

  1. Review
  2. Article
  3. 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

11 authors at 2 institutions in 1 country.

Chi-Sheng LuDepartments of Medical Research, Mackay Memorial Hospital, Taipei, 10449, Taiwan.
Yi-Nan LeeDepartments of Medical Research, Mackay Memorial Hospital, Taipei, 10449, Taiwan.
Shin-Wei WangDepartment of Medicine, Mackay Medical College, New Taipei City, 25245, Taiwan.
Yih-Jer WuDepartments of Medical Research, Mackay Memorial Hospital, Taipei, 10449, Taiwan.
Cheng-Huang SuDepartments of Medical Research, Mackay Memorial Hospital, Taipei, 10449, Taiwan.
Chin-Ling HsiehDepartments of Medical Research, Mackay Memorial Hospital, Taipei, 10449, Taiwan.
Ting Yi TienDepartments of Medical Research, Mackay Memorial Hospital, Taipei, 10449, Taiwan.
Bo-Jeng WangDepartment of Medicine, Mackay Medical College, New Taipei City, 25245, Taiwan.
Min-Che ChenAsclepiumm Taiwan Co., Ltd, New Taipei City, 25160, Taiwan.
Chun-Wei ChenAsclepiumm Taiwan Co., Ltd, New Taipei City, 25160, Taiwan.
Hung-I YehDepartments of Medical Research, Mackay Memorial Hospital, Taipei, 10449, Taiwan. hiyeh@mmh.org.tw.ORCID 0000-0003-3206-0908
Mackay Memorial Hospital · TWMackay Medical University · TW

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Desmogleins (Dsg2) are the major components of desmosomes. Dsg2 has five extracellular tandem cadherin domains (EC1-EC5) for cell-cell interaction. We had previously confirmed the Dsg2 antibody and its epitope (named KC21) derived from EC2 domain suppressing epithelial-mesenchymal transition and invasion in human cancer cell lines. Here, we screened six peptide fragments derived from EC2 domain and found that KR20, the parental peptide of KC21, was the most potent one on suppressing endothelial colony-forming cell (ECFC) tube-like structure formation. KC21 peptide also attenuated migration but did not disrupt viability and proliferation of ECFCs, consistent with the function to inhibit VEGF-mediated activation of p38 MAPK but not AKT and ERK. Animal studies showed that KC21 peptides suppressed capillary growth in Matrigel implant assay and inhibited oxygen-induced retinal neovascularization. The effects were comparable to bevacizumab (Bev). In conclusion, KC21 peptide is an angiogenic inhibitor potentially useful for treating angiogenesis-related diseases.

Indexed as

Angiogenesis InhibitorsAnimalsBevacizumabCell MovementCell ProliferationCells, CulturedDesmoglein 2Disease Models, AnimalEndothelial Progenitor CellsHumansHypoxiaMatrix Metalloproteinase 9Mice, Inbred C57BLNeovascularization, Physiologicp38 Mitogen-Activated Protein KinasesPeptide FragmentsAngiogenesis InhibitorsBevacizumabDesmoglein 2Matrix Metalloproteinase 9MMP9 protein, humanp38 Mitogen-Activated Protein KinasesPeptide FragmentsAngiogenesisDesmoglein-2Endothelial colony-forming cellsNeovascularizationTherapeutic peptide

Identifiers

PMID30790141
PMCPMC6707963
OpenAlexW2916901429

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.