Evidence map›Paper›PMID 27654896›Full record

ReviewAmerican journal of physiology. Renal physiology2017

Blocking peptides and molecular mimicry as treatment for kidney disease.

Andrea Havasi, Weining Lu, Herbert T Cohen, Laurence Beck, Zhiyong Wang, Chinaemare Igwebuike, Steven C Borkan

Open access · bronzeAbstract readReview
In one paragraph

Review in American journal of physiology. Renal physiology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.2field-weighted citation impact, top 37% 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

4 citing papers in PubMed, 6 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Nucleophosmin Phosphorylation as a Diagnostic and Therapeutic Target for Ischemic AKI.Journal of the American Society of Nephrology : JASN · 2019
    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

7 authors at 2 institutions in 1 country.

Andrea HavasiRenal Section, Boston University Medical Center, Boston, Massachusetts.
Weining LuRenal Section, Boston University Medical Center, Boston, Massachusetts.
Herbert T CohenRenal Section, Boston University Medical Center, Boston, Massachusetts.
Laurence BeckRenal Section, Boston University Medical Center, Boston, Massachusetts.
Zhiyong WangRenal Section, Boston University Medical Center, Boston, Massachusetts.
Chinaemare IgwebuikeRenal Section, Boston University Medical Center, Boston, Massachusetts.
Steven C BorkanRenal Section, Boston University Medical Center, Boston, Massachusetts sborkan@bu.edu.
Boston Medical Center · USUniversity Medical Center · US

Funding

CYTOPROTECTIVE ROLE OF HSP72 IN RENAL CELL INJURYR01DK053387 · NIDDK · BOSTON MEDICAL CENTER · PI BORKAN, STEVEN C. · 1999 to 2016
$5.1M
Molecular Pathogenesis of Vesicoureteral RefluxR01DK078226 · NIDDK · BOSTON MEDICAL CENTER · PI LU, WEINING · 2008 to 2018
$2.5M
Proteinuria causes progressive kidney disease by impairing autophagyK08DK090143 · NIDDK · BOSTON MEDICAL CENTER · PI HAVASI, ANDREA · 2011 to 2015
$746k
Prevention and Treatment of Antibiotic-Induced Acute Kidney Injury Using an Unbiased Gene-Screen StrategyF30DK117612 · NIDDK · BOSTON UNIVERSITY MEDICAL CAMPUS · PI IGWEBUIKE, CHINAEMERE · 2019 to 2021
$152k
NIDDK NIH HHS F30 DK117612NIDDK NIH HHS K08 DK090143NIDDK NIH HHS R01 DK053387NIDDK NIH HHS R01 DK078226
6 · The paper itself

Abstract

Protein mimotopes, or blocking peptides, are small therapeutic peptides that prevent protein-protein interactions by selectively mimicking a native binding domain. Inexpensive technology facilitates straightforward design and production of blocking peptides in sufficient quantities to allow preventive and therapeutic trials in both in vitro and in vivo experimental disease models. The kidney is an ideal peptide target, since small molecules undergo rapid filtration and efficient bulk absorption by tubular epithelial cells. Because the half-life of peptides is markedly prolonged in the kidneys compared with the bloodstream, blocking peptides are an attractive tool for treating diverse renal diseases, including ischemia, proteinuric states, such as membranous nephropathy and focal and segmental glomerulosclerosis, and renal cell carcinoma. Therapeutic peptides represent one of the fastest-growing reagent classes for novel drug development in human disease, partly because of their ease of administration, high binding affinity, and minimal off-target effects. This review introduces the concepts of blocking peptide design, production, and administration and highlights the potential use of therapeutic peptides to prevent or treat specific renal diseases.

Indexed as

Molecular MimicryAnimalsHumansKidneyKidney DiseasesMolecular Targeted TherapyPeptidesProtein BindingProtein Interaction Domains and MotifsSignal TransductionUrological AgentsPeptidesUrological Agentsacute kidney injuryBaxfoot processischemiaJade-1membranous nephropathynucleophosminphospholipase A2 receptorpodocyterenal cell carcinomaslit diaphragm

Identifiers

PMID27654896
PMCPMC5495884
OpenAlexW2522991972

What OpenQuestion holds

Textmetadata
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.