Evidence map›Paper›PMID 23452816›Full record

ReviewTrends in pharmacological sciences2013

β-Secretase: its biology as a therapeutic target in diseases.

Haibo Wang, Rena Li, Yong Shen

Open access · greenAbstract readReview
In one paragraph

Review in Trends in pharmacological sciences, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
2.9field-weighted citation impact, top 9% 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

29 citing papers in PubMed, 70 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Review
  5. Article
  6. BACE1: More than just a β-secretase.Obesity reviews : an official journal of the International Association for the Study of Obesity · 2022
    Review
  7. Article
  8. Review
  9. Neuroactive venom compounds obtained fromThe journal of venomous animals and toxins including tropical diseases · 2021
    Article
  10. Article
  11. Article
  12. PotentBioMed research international · 2020
    Article
  13. Article
  14. Review
  15. Article
  16. Article
  17. Amyloid precursor protein and endosomal-lysosomal dysfunction in Alzheimer's disease: inseparable partners in a multifactorial disease.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2017
    Review
  18. Review
  19. Review
  20. 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

3 authors at 1 institution in 1 country.

Haibo WangCenter for Advanced Therapeutic Strategies for Brain Disorders, Roskamp Institute, Sarasota, FL 34203, USA.
Rena Li
Yong Shen
Roskamp Institute · US

Funding

Novel roles of TNF death receptor in amyloidosis in vivoR01AG025888 · NIA · ROSKAMP INSTITUTE, INC. · PI SHEN, YONG · 2006 to 2014
$3.2M
Study on Thalidomide as BACE1 inhibitor in Alzhiemer's diseaseR01AG034155 · NIA · BANNER SUN HEALTH RESEARCH INSTITUTE · PI SABBAGH, MARWAN NOEL · 2009 to 2010
$1.7M
The role of estrogen receptors in Alzheimer?s diseaseR01AG032441 · NIA · ROSKAMP INSTITUTE, INC. · PI LI, RENA · 2009 to 2012
$1.3M
NIA NIH HHS R01 AG025888NIA NIH HHS R01AG025888NIA NIH HHS R01 AG032441NIA NIH HHS R01AG032441NIA NIH HHS R01 AG034155
6 · The paper itself

Abstract

β-Secretase (BACE1, β-site APP cleaving enzyme 1) is an aspartic proteinase that has multiple functions in various physiological processes, such as cell differentiation, immunoregulation, and cell death. There is increasing evidence that changes in BACE1 activity are involved in many diseases, such as Alzheimer's disease (AD), schizophrenia, epileptic behavior, and others. However, a deeper understanding of the molecular biology of BACE1 is necessary for further exploration of cell development, immunological regulation, and disease pathogenesis. Here, we review the molecular and cellular biology of BACE1, including its enzymatic properties, structure, biosynthesis, and physiological functions to provide a new perspective and rational assessment of drugability. Lastly, we discuss proposed strategies to control BACE1 activity for possible therapeutic application.

Indexed as

Amino Acid SequenceAmyloid Precursor Protein SecretasesAnimalsAspartic Acid EndopeptidasesHumansModels, MolecularMolecular Sequence DataMolecular Targeted TherapyAmyloid Precursor Protein SecretasesAspartic Acid EndopeptidasesBACE1 protein, human

Identifiers

PMID23452816
PMCPMC3691103
OpenAlexW2087451417

What OpenQuestion holds

Textmetadata
LicenceTDM
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.