Evidence map›Paper›PMID 30279592›Full record

ArticleScientific reports2018

Effect of Differences in Metabolic Activity of Melanoma Models on Response to Lonidamine plus Doxorubicin.

Kavindra Nath, Jeffrey Roman, David S Nelson, Lili Guo, Seung-Cheol Lee, Stepan Orlovskiy, Kevin Muriuki, Daniel F Heitjan, Stephen Pickup, Dennis B Leeper and 3 more

Open access · goldAbstract readComparative Study
In one paragraph

Article in Scientific reports, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
0.3field-weighted citation impact, top 42% 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

9 citing papers in PubMed, 12 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Review
  9. 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

13 authors at 4 institutions in 1 country.

Kavindra NathDepartment of Radiology, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA. kavindra.nath@uphs.upenn.edu.
Jeffrey RomanDepartment of Radiology, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA.
David S NelsonDepartment of Radiology, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA.
Lili GuoCenter of Excellence in Environmental Toxicology and Department of Systems Pharmacology and Translational Therapeutics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA.
Seung-Cheol LeeDepartment of Radiology, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA.
Stepan OrlovskiyDepartment of Radiology, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA.
Kevin MuriukiDepartment of Radiology, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA.
Daniel F HeitjanDepartment of Statistical Science, Southern Methodist University, Dallas, TX, USA.
Stephen PickupDepartment of Radiology, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA.
Dennis B LeeperDepartment of Radiation Oncology, Thomas Jefferson University, Philadelphia, PA, USA.
Ian A BlairCenter of Excellence in Environmental Toxicology and Department of Systems Pharmacology and Translational Therapeutics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA.
Mary E PuttBiostatistics & Epidemiology, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA.
Jerry D GlicksonDepartment of Radiology, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA.
University of Pennsylvania · USSouthwestern Medical CenterThomas Jefferson University · USTranslational Therapeutics (United States) · US

Funding

UNIVERSITY OF PENNSYLVANIA CAN CTR SUPPORT GRANTP30CA016520 · NCI · UNIVERSITY OF PENNSYLVANIA · PI SHELLEY L BERGER · 1985 to 2026
$222.3M
Systemic Chemotherapy of Melanoma: NMR Studies of Lonidamine & N-Mustard ActivityR01CA129544 · NCI · UNIVERSITY OF PENNSYLVANIA · PI GLICKSON, JERRY D · 2009 to 2016
$3.2M
Mechanism of Activity of LonidamineR01CA172820 · NCI · UNIVERSITY OF PENNSYLVANIA · PI GLICKSON, JERRY D · 2013 to 2017
$2.8M
NCI NIH HHS P30 CA016520NCI NIH HHS R01 CA129544NCI NIH HHS R01 CA172820U.S. Department of Health & Human Services | NIH | National Cancer Institute (NCI) R01-CA172544U.S. Department of Health & Human Services | NIH | National Cancer Institute (NCI) R01-CA172820
6 · The paper itself

Abstract

Lonidamine (LND), a metabolic modulator, sensitizes DB-1 human melanoma to doxorubicin (DOX) chemotherapy by acidifying and de-energizing the tumor. This report compares the effects of LND on two human melanoma lines, DB-1 and WM983B, which exhibit different metabolic properties. Using liquid chromatography mass spectrometry and Seahorse analysis, we show that DB-1 was more glycolytic than WM983B in vitro.

Indexed as

AnimalsAntineoplastic Combined Chemotherapy ProtocolsCell Line, TumorDoxorubicinDrug SynergismEnergy MetabolismGlucoseGlycolysisHumansHydrogen-Ion ConcentrationIndazolesLactic AcidMagnetic Resonance SpectroscopyMaleMelanomaMiceDoxorubicinGlucoseIndazolesLactic AcidlonidamineOxygen

Identifiers

PMID30279592
PMCPMC6168452
OpenAlexW2893074769

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.