Evidence map›Paper›PMID 35807522›Full record

ArticleMolecules (Basel, Switzerland)2022

Chemometric Analysis of Urinary Volatile Organic Compounds to Monitor the Efficacy of Pitavastatin Treatments on Mammary Tumor Progression over Time.

Paul Grocki, Mark Woollam, Luqi Wang, Shengzhi Liu, Maitri Kalra, Amanda P Siegel, Bai-Yan Li, Hiroki Yokota, Mangilal Agarwal

Open access · goldAbstract read
In one paragraph

Article in Molecules (Basel, Switzerland), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.5field-weighted citation impact, top 43% 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

2 citing papers in PubMed, 6 citations in OpenAlex.

  1. Review
  2. 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

9 authors at 3 institutions in 2 countries.

Paul GrockiDepartment of Chemistry and Chemical Biology, Indiana University-Purdue University, Indianapolis, IN 46202, USA.
Mark WoollamDepartment of Chemistry and Chemical Biology, Indiana University-Purdue University, Indianapolis, IN 46202, USA.
Luqi WangDepartment of Pharmacology, School of Pharmacy, Harbin Medical University, Harbin 150081, China.
Shengzhi LiuDepartment of Pharmacology, School of Pharmacy, Harbin Medical University, Harbin 150081, China.
Maitri KalraHematology and Oncology, Ball Memorial Hospital, Indiana University Health, Muncie, IN 47303, USA.
Amanda P SiegelDepartment of Chemistry and Chemical Biology, Indiana University-Purdue University, Indianapolis, IN 46202, USA.ORCID 0000-0003-4112-0212
Bai-Yan LiDepartment of Pharmacology, School of Pharmacy, Harbin Medical University, Harbin 150081, China.ORCID 0000-0002-1853-0216
Hiroki YokotaIntegrated Nanosystems Development Institute, Indiana University-Purdue University, Indianapolis, IN 46202, USA.ORCID 0000-0002-7881-8959
Mangilal AgarwalDepartment of Chemistry and Chemical Biology, Indiana University-Purdue University, Indianapolis, IN 46202, USA.
Indiana University – Purdue University Indianapolis · USHarbin Medical University · CNIndiana University Health · US

Funding

MECHANICAL LOADING AND BONER01AR052144 · NIAMS · INDIANA UNIV-PURDUE UNIV AT INDIANAPOLIS · PI YOKOTA, HIROKI · 2006 to 2018
$4.2M
National Institute of Health (NIH)/National Institute of Arthritis and Musculoskeletal and Skin Diseases R01AR052144National Science Foundation 1502310National Science Foundation 1852105NIAMS NIH HHS R01 AR052144
6 · The paper itself

Abstract

Volatile organic compounds (VOCs) in urine are potential biomarkers of breast cancer. Previously, our group has investigated breast cancer through analysis of VOCs in mouse urine and identified a panel of VOCs with the ability to monitor tumor progression. However, an unanswered question is whether VOCs can be exploited similarly to monitor the efficacy of antitumor treatments over time. Herein, subsets of tumor-bearing mice were treated with pitavastatin at high (8 mg/kg) and low (4 mg/kg) concentrations, and urine was analyzed through solid-phase microextraction (SPME) coupled with gas chromatography-mass spectrometry (GC-MS). Previous investigations using X-ray and micro-CT analysis indicated pitavastatin administered at 8 mg/kg had a protective effect against mammary tumors, whereas 4 mg/kg treatments did not inhibit tumor-induced damage. VOCs from mice treated with pitavastatin were compared to the previously analyzed healthy controls and tumor-bearing mice using chemometric analyses, which revealed that mice treated with pitavastatin at high concentrations were significantly different than tumor-bearing untreated mice in the direction of healthy controls. Mice treated with low concentrations demonstrated significant differences relative to healthy controls and were reflective of tumor-bearing untreated mice. These results show that urinary VOCs can accurately and noninvasively predict the efficacy of pitavastatin treatments over time.

Indexed as

Mammary Neoplasms, AnimalVolatile Organic CompoundsAnimalsChemometricsGas Chromatography-Mass SpectrometryMiceQuinolinesSolid Phase MicroextractionpitavastatinQuinolinesVolatile Organic Compoundsbreast cancer biomarkersgas chromatography (GC)linear discriminant analysis (LDA)mass spectrometry (MS)pitavastatinprincipal component analysis (PCA)solid-phase microextraction (SPME)volatile organic compounds (VOCs)

Identifiers

PMID35807522
PMCPMC9268606
OpenAlexW4283813706

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.