Evidence map›Paper›PMID 24107651›Full record

ArticleCancer biology & therapy2014

Infrared microspectroscopy identifies biomolecular changes associated with chronic oxidative stress in mammary epithelium and stroma of breast tissues from healthy young women: implications for latent stages of breast carcinogenesis.

Imran I Patel, Debra A Shearer, Simon W Fogarty, Nigel J Fullwood, Luca Quaroni, Francis L Martin, Judith Weisz

Open access · bronzeAbstract read
In one paragraph

Article in Cancer biology & therapy, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
1.3field-weighted citation impact, top 19% 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

4 citing papers in PubMed, 21 citations in OpenAlex.

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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

7 authors at 4 institutions in 3 countries.

Imran I PatelCenter for Biophotonics; Lancaster Environment Centre; Lancaster University; Lancaster, UK.
Debra A ShearerDepartment of Obstetrics and Gynecology; College of Medicine; Pennsylvania State University; Hershey, PA USA.
Simon W FogartyDivision of Biomedical and Life Sciences; Faculty of Health and Medicine; Lancaster University; Lancaster, UK.
Nigel J FullwoodDivision of Biomedical and Life Sciences; Faculty of Health and Medicine; Lancaster University; Lancaster, UK.
Luca QuaroniPaul Scherrer Institut; Villigen, Switzerland.
Francis L MartinCenter for Biophotonics; Lancaster Environment Centre; Lancaster University; Lancaster, UK.
Judith WeiszDepartment of Obstetrics and Gynecology; College of Medicine; Pennsylvania State University; Hershey, PA USA; Department of Pathology; College of Medicine; Pennsylvania State University; Hershey, PA USA.
Lancaster University · GBHershey (United States) · USPaul Scherrer Institute · CHPennsylvania State University · US

Funding

Biotechnology and Biological Sciences Research Council
6 · The paper itself

Abstract

Studies of the decades-long latent stages of breast carcinogenesis have been limited to when hyperplastic lesions are already present. Investigations of earlier stages of breast cancer (BC) latency have been stymied by the lack of fiducial biomarkers needed to identify where in histologically normal tissues progression toward a BC might be taking place. Recent evidence suggests that a marker of chronic oxidative stress (OxS), protein adducts of 4-hydroxy-2-nonenal (4HNE), can meet this need. Specifically: (1) 4HNE immunopositive (4HNE+) mammary epithelial (ME) cells were found to be prevalent in normal (reduction mammoplasty) tissues of most women (including many teenagers) studied, representative of those living in the United States' high risk-posing environment and: (2) marked (> 1.5-fold) differences were identified between tissues of healthy young women with many vs. few 4HNE+ ME cells in the relative levels of transcripts for 42 of the 84 OxS-associated genes represented in SABioscience Oxidative-Stress/Oxidative-Defense PCR array. Herein we used synchrotron radiation-based Fourier-transform infrared (SR-FTIR) microspectroscopy to identify molecular changes associated with 4HNE adducts in basal and luminal ME cells in terminal ductal units (TDLU), which are the cells of origin of BC, and associated intralobular and interlobular stroma, known contributors to carcinogenesis. Multivariate analysis-derived wavenumbers differentiated 4HNE+ and 4HNE- cells in each of the anatomical compartments. Specifically, principal component and linear discriminant analyses of mid-infrared spectra obtained from these cells revealed unambiguous, statistically highly significant differences in the "biochemical fingerprint" of 4HNE+ vs. 4HNE- luminal and basal ME cells, as well as between associated intralobular and interlobular stroma. These findings demonstrate further SR-FTIR microspectroscopy's ability to identify molecular changes associated with altered physiological and/or pathophysiological states, in this case with a state of chronic OxS that provides a pro-carcinogenic microenvironment.

Indexed as

Oxidative StressAdultAldehydesBiomarkersBreastBreast NeoplasmsCell Transformation, NeoplasticEpithelial CellsFemaleHumansIn Vitro TechniquesReference ValuesSpectroscopy, Fourier Transform InfraredStromal CellsYoung Adult4-hydroxy-2-nonenalAldehydesBiomarkersadaptation to chronic oxidative stressbiochemical-cell fingerprintbreast carcinogenesischronic oxidative stressevolutionary model of carcinogenesisFourier-transform infrared microspectroscopysynchrotron radiation

Identifiers

PMID24107651
PMCPMC3928139
OpenAlexW2316370248

What OpenQuestion holds

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Registered trials

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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.