Evidence map›Paper›PMID 31135523›Full record

ReviewCancer journal (Sudbury, Mass.)

Inhibiting Autophagy in Renal Cell Cancer and the Associated Tumor Endothelium.

Kira L Russell, Carolina Mendonça Gorgulho, Abigail Allen, Marianna Vakaki, Yue Wang, Andrea Facciabene, Daniel Lee, Partha Roy, William J Buchser, Leonard J Appleman and 3 more

Open access · greenAbstract readReview
In one paragraph

Review in Cancer journal (Sudbury, Mass.). The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.8field-weighted citation impact, top 27% 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

5 citing papers in PubMed, 7 citations in OpenAlex.

  1. Article
  2. Article
  3. An actin-WHAMM interaction linking SETD2 and autophagy.Biochemical and biophysical research communications · 2021
    Article
  4. Article
  5. 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

13 authors at 3 institutions in 1 country.

Kira L Russell
Carolina Mendonça Gorgulho
Abigail AllenBioengineering, University of Pittsburgh, Pittsburgh, PA.
Marianna VakakiDepartment of Genetics, Washington University, St Louis, MO.
Yue Wang
Andrea FacciabeneDepartment of Radiation Oncology, University of Pennsylvania, Philadelphia, PA.
Daniel LeeDepartments of Medicine.
Partha RoyBioengineering, University of Pittsburgh, Pittsburgh, PA.
William J BuchserDepartment of Genetics, Washington University, St Louis, MO.
Leonard J ApplemanDepartments of Medicine.
Jodi MaranchieUrology.
Walter J StorkusDermatology, University of Pittsburgh, Pittsburgh, PA.
Michael T Lotze
University of Pittsburgh · USWashington University in St. Louis · USUniversity of Pennsylvania · US

Funding

Profilin as a target to suppress Invasive breast cancerR01CA108607 · NCI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI ROY, PARTHA · 2006 to 2017
$2.6M
(PQ5) Mitochondria are endocellular symbionts that serve as targets for immune recognitionR01CA206012 · NCI · UNIVERSITY OF PENNSYLVANIA · PI FACCIABENE, ANDREA · 2016 to 2020
$2.0M
Profilin-1's Role in AtherosclerosisF31HL160118 · NHLBI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI GONDRINGER, ABIGAIL ELIZABETH ALLEN · 2021 to 2023
$103k
NCI NIH HHS R01 CA108607NCI NIH HHS R01 CA206012NHLBI NIH HHS F31 HL160118
6 · The paper itself

Abstract

The clear cell subtype of kidney cancer encompasses most renal cell carcinoma cases and is associated with the loss of von Hippel-Lindau gene function or expression. Subsequent loss or mutation of the other allele influences cellular stress responses involving nutrient and hypoxia sensing. Autophagy is an important regulatory process promoting the disposal of unnecessary or degraded cellular components, tightly linked to almost all cellular processes. Organelles and proteins that become damaged or that are no longer needed in the cell are sequestered and digested in autophagosomes upon fusing with lysosomes, or alternatively, released via vesicular exocytosis. Tumor development tends to disrupt the regulation of the balance between this process and apoptosis, permitting prolonged cell survival and increased replication. Completed trials of autophagic inhibitors using hydroxychloroquine in combination with other anticancer agents including rapalogues and high-dose interleukin 2 have now been reported. The complex nature of autophagy and the unique biology of clear cell renal cell carcinoma warrant further understanding to better develop the next generation of relevant anticancer agents.

Indexed as

AutophagyAnimalsAntineoplastic AgentsBiomarkersCarcinoma, Renal CellClinical Trials as TopicCytoskeletonDisease SusceptibilityDrug DiscoveryDrug Screening Assays, AntitumorEndotheliumHigh-Throughput Nucleotide SequencingHumansKidney NeoplasmsMitochondriaMitophagyAntineoplastic AgentsBiomarkersVon Hippel-Lindau Tumor Suppressor Protein

Identifiers

PMID31135523
PMCPMC10395074
OpenAlexW2946692098

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.