Evidence map›Paper›PMID 26689099›Full record

ReviewFuture medicinal chemistry2016

Leaving the lysosome behind: novel developments in autophagy inhibition.

Abigail R Solitro, Jeffrey P MacKeigan

Open access · hybridAbstract readReview
In one paragraph

Review in Future medicinal chemistry, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
3.7field-weighted citation impact, top 6% 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

26 citing papers in PubMed, 56 citations in OpenAlex.

  1. Article
  2. Review
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  5. Review
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  8. Lysosomal inhibition sensitizes TMEM16A-expressing cancer cells to chemotherapy.Proceedings of the National Academy of Sciences of the United States of America · 2022
    Article
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  10. Review
  11. Article
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  14. Review
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  18. Review
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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

2 authors at 1 institution in 1 country.

Abigail R SolitroCenter for Cancer & Cell Biology, Van Andel Research Institute, 333 Bostwick Avenue, Grand Rapids, MI 49503, USA.
Jeffrey P MacKeiganCenter for Cancer & Cell Biology, Van Andel Research Institute, 333 Bostwick Avenue, Grand Rapids, MI 49503, USA.
Van Andel Institute · US

Funding

Computational Model of Autophagy-Mediated Survival in Chemoresistant Lung CancerR01CA197398 · NCI · VAN ANDEL RESEARCH INSTITUTE · PI HLAVACEK, WILLIAM S, MACKEIGAN, JEFFREY PAUL · 2015 to 2019
$2.5M
NCI NIH HHS R01 CA197398NCI NIH HHS R01CA197398
6 · The paper itself

Abstract

The search for a single silver bullet for the treatment of cancer has now been overshadowed by the identification of multiple therapeutic targets unique to each malignancy and even to each patient. In recent years, autophagy has emerged as one such therapeutic target. In response to both therapeutic and oncogenic stress, cancer cells upregulate and demonstrate an increased dependence upon this intracellular recycling process. Particularly in malignancies that currently lack targeted therapeutic options, autophagy inhibitors are the next hopeful prospects for the treatment of this disease. In this review, we discuss the rapid evolution of autophagy inhibitors from early lysosomotropic agents to next-generation lysosome-targeted drugs and beyond.

Indexed as

AnimalsAntimalarialsAntineoplastic AgentsAutophagyHumansLysosomesNeoplasmsStructure-Activity RelationshipAntimalarialsAntineoplastic Agents

Identifiers

PMID26689099
PMCPMC4886745
OpenAlexW2238831297

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.