Evidence map›Paper›PMID 28369883›Full record

ArticleJournal of cellular physiology2017

Individual-specific variation in the respiratory activities of HMECs and their bioenergetic response to IGF1 and TNFα.

Sallie S Schneider, Elizabeth M Henchey, Nazneen Sultana, Stephanie M Morin, D Joseph Jerry, Grace Makari-Judson, Giovanna M Crisi, Richard B Arenas, Melissa Johnson, Holly S Mason and 1 more

Open access · hybridAbstract readComparative Study
In one paragraph

Article in Journal of cellular physiology, 2017. 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
0.1field-weighted citation impact, top 51% 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, 3 citations in OpenAlex.

  1. Article
  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

11 authors at 3 institutions in 1 country.

Sallie S SchneiderPioneer Valley Life Sciences Institute (PVLSI), Springfield, Massachusetts.
Elizabeth M HencheyPioneer Valley Life Sciences Institute (PVLSI), Springfield, Massachusetts.
Nazneen SultanaPioneer Valley Life Sciences Institute (PVLSI), Springfield, Massachusetts.
Stephanie M MorinPioneer Valley Life Sciences Institute (PVLSI), Springfield, Massachusetts.
D Joseph JerryPioneer Valley Life Sciences Institute (PVLSI), Springfield, Massachusetts.
Grace Makari-JudsonDivision of Hematology Oncology, Department of Medicine at Baystate Medical Center/Tufts University School of Medicine, Springfield, Massachusetts.
Giovanna M CrisiDivision of Anatomic and Clinical Pathology, Department of Pathology at University of Massachusetts Medical School (UMMS)-Baystate Regional Campus, Springfield, Massachusetts.
Richard B ArenasDivision of Surgical Oncology, Department of Surgery at University of Massachusetts Medical School (UMMS)-Baystate Regional Campus, Springfield, Massachusetts.
Melissa JohnsonPioneer Valley Plastic Surgery, Springfield, Massachusetts.
Holly S MasonDivision of Surgical Oncology, Department of Surgery at University of Massachusetts Medical School (UMMS)-Baystate Regional Campus, Springfield, Massachusetts.
Nagendra YadavaPioneer Valley Life Sciences Institute (PVLSI), Springfield, Massachusetts.ORCID http://orcid.org/0000-0002-6202-2673
Pioneer (United States) · USUniversity of Massachusetts Chan Medical School · USTufts University · US

Funding

Metabolomics Administrative Supplement: Disruption of parity-induced tumor suppressor pathways by xenoestrogen exposures during pregnancyU01ES026140 · NIEHS · UNIVERSITY OF MASSACHUSETTS AMHERST · PI JERRY, D. JOSEPH, SCHNEIDER, SALLIE SMITH · 2015 to 2019
$3.7M
NIEHS NIH HHS U01 ES026140
6 · The paper itself

Abstract

Metabolic reprograming is a hallmark of cancer cells. However, the roles of pre-existing differences in normal cells metabolism toward cancer risk is not known. In order to assess pre-existing variations in normal cell metabolism, we have quantified the inter-individual variation in oxidative metabolism of normal primary human mammary epithelial cells (HMECs). We then assessed their response to selected cytokines such as insulin growth factor 1 (IGF1) and tumor necrosis factor alpha (TNFα), which are associated with breast cancer risk. Specifically, we compared the oxidative metabolism of HMECs obtained from women with breast cancer and without cancer. Our data show considerable inter-individual variation in respiratory activities of HMECs from different women. A bioenergetic parameter called pyruvate-stimulated respiration (PySR) was identified as a key distinguishing feature of HMECs from women with breast cancer and without cancer. Samples showing PySR over 20% of basal respiration rate were considered PySR

Indexed as

AdultAgedBreast NeoplasmsCell RespirationEnergy MetabolismEpithelial CellsFemaleHumansInsulin-Like Growth Factor IMammary Glands, HumanMetabolomicsMiddle AgedOxidation-ReductionPhenotypePyruvic AcidTime FactorsInsulin-Like Growth Factor IPyruvic AcidTumor Necrosis Factor-alphabioenergeticshuman mammary epithelial cells (HMECs)IGF1oxidative phosphorylationrespirationrespiratory chainTNFα

Identifiers

PMID28369883
PMCPMC5518214
OpenAlexW2598362916

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.