Evidence map›Paper›PMID 26040322›Full record

ArticleBreast cancer research : BCR2015

High mammographic density is associated with an increase in stromal collagen and immune cells within the mammary epithelium.

Cecilia W Huo, Grace Chew, Prue Hill, Dexing Huang, Wendy Ingman, Leigh Hodson, Kristy A Brown, Astrid Magenau, Amr H Allam, Ewan McGhee and 4 more

Open access · goldAbstract read
In one paragraph

Article in Breast cancer research : BCR, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 110 papers.

0numbers the graph read from it
0cells of the map it votes in
110citing papers in PubMed
13.5field-weighted citation impact, top 1% 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

110 citing papers in PubMed, 173 citations in OpenAlex.

  1. Trial
  2. Trial
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Review
  11. Article
  12. Review
  13. Article
  14. Review
  15. Observational
  16. Article
  17. Review
  18. Article
  19. SubvertingBiology · 2024
    Review
  20. Review

50 more citing papers are in PubMed but not listed here.

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

14 authors at 10 institutions in 2 countries.

Cecilia W HuoUniversity of Melbourne Department of Surgery, St. Vincent's Hospital, Level 2, Clinical Sciences Building, 29 Regent Street, Fitzroy, VIC, 3065, Australia. wanchen.huo@gmail.com.
Grace ChewUniversity of Melbourne Department of Surgery, St. Vincent's Hospital, Level 2, Clinical Sciences Building, 29 Regent Street, Fitzroy, VIC, 3065, Australia. gracelchew@gmail.com.
Prue HillDepartment of Pathology, St. Vincent's Hospital, 41 Victoria Parade, Fitzroy, VIC, 3065, Australia. prue.hill@svha.org.au.
Dexing HuangSt. Vincent's Institute, 9 Princes Street, Fitzroy, VIC, 3065, Australia. dhuang@svi.edu.au.
Wendy IngmanDiscipline of Surgery, Faculty of Health Sciences, School of Medicine, The Queen Elizabeth Hospital, University of Adelaide, Adelaide, Australia. wendy.ingman@adelaide.edu.au.
Leigh HodsonDiscipline of Surgery, Faculty of Health Sciences, School of Medicine, The Queen Elizabeth Hospital, University of Adelaide, Adelaide, Australia. leigh.hodson@adelaide.edu.au.
Kristy A BrownHudson Institute of Medical Research, 27-31 Wright Street, Clayton, VIC, 3168, Australia. kristy.brown@mimr-phi.org.
Astrid MagenauGarvan Institute of Medical Research, 384 Victoria Street, Darlinghurst, Australia. a.magenau@garvan.org.au.
Amr H AllamGarvan Institute of Medical Research, 384 Victoria Street, Darlinghurst, Australia. a.allam@garvan.org.au.
Ewan McGheeSt Vincent's Clinical School, Faculty of Medicine, University of NSW, Sydney, Australia. e.mcghee@beatson.gla.ac.uk.
Paul TimpsonGarvan Institute of Medical Research, 384 Victoria Street, Darlinghurst, Australia. p.timpson@garvan.org.au.
Michael A HendersonUniversity of Melbourne Department of Surgery, St. Vincent's Hospital, Level 2, Clinical Sciences Building, 29 Regent Street, Fitzroy, VIC, 3065, Australia. michael.henderson@petermac.org.
Erik W ThompsonUniversity of Melbourne Department of Surgery, St. Vincent's Hospital, Level 2, Clinical Sciences Building, 29 Regent Street, Fitzroy, VIC, 3065, Australia. e2.thompson@qut.edu.au.
Kara BrittThe Beatson Institute for Cancer Research, Switchback Road, Bearsden Glasgow, G61 1BD, UK. kara.britt@petermac.org.
Garvan Institute of Medical Research · AUSt Vincents Institute of Medical Research · AUUniversity of Melbourne · AUCancer Research UK Scotland Institute · GBHudson Institute of Medical Research · AUPeter MacCallum Cancer Centre · AUQueen Elizabeth Hospital · AUSt Vincent's Clinic · AUSt Vincent's Hospital · AUUniversity of Adelaide · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionMammographic density (MD), after adjustment for a women's age and body mass index, is a strong and independent risk factor for breast cancer (BC). Although the BC risk attributable to increased MD is significant in healthy women, the biological basis of high mammographic density (HMD) causation and how it raises BC risk remain elusive. We assessed the histological and immunohistochemical differences between matched HMD and low mammographic density (LMD) breast tissues from healthy women to define which cell features may mediate the increased MD and MD-associated BC risk.

methodsTissues were obtained between 2008 and 2013 from 41 women undergoing prophylactic mastectomy because of their high BC risk profile. Tissue slices resected from the mastectomy specimens were X-rayed, then HMD and LMD regions were dissected based on radiological appearance. The histological composition, aromatase immunoreactivity, hormone receptor status and proliferation status were assessed, as were collagen amount and orientation, epithelial subsets and immune cell status.

resultsHMD tissue had a significantly greater proportion of stroma, collagen and epithelium, as well as less fat, than LMD tissue did. Second harmonic generation imaging demonstrated more organised stromal collagen in HMD tissues than in LMD tissues. There was significantly more aromatase immunoreactivity in both the stromal and glandular regions of HMD tissues than in those regions of LMD tissues, although no significant differences in levels of oestrogen receptor, progesterone receptor or Ki-67 expression were detected. The number of macrophages within the epithelium or stroma did not change; however, HMD stroma exhibited less CD206(+) alternatively activated macrophages. Epithelial cell maturation was not altered in HMD samples, and no evidence of epithelial-mesenchymal transition was seen; however, there was a significant increase in vimentin(+)/CD45(+) immune cells within the epithelial layer in HMD tissues.

conclusionsWe confirmed increased proportions of stroma and epithelium, increased aromatase activity and no changes in hormone receptor or Ki-67 marker status in HMD tissue. The HMD region showed increased collagen deposition and organisation as well as decreased alternatively activated macrophages in the stroma. The HMD epithelium may be a site for local inflammation, as we observed a significant increase in CD45(+)/vimentin(+) immune cells in this area.

Indexed as

AdultBiomarkers, TumorBreastBreast DensityBreast NeoplasmsCollagenEpithelial-Mesenchymal TransitionEpitheliumFemaleHumansImmunohistochemistryImmunophenotypingMacrophagesMammary Glands, HumanMammographyMiddle AgedBiomarkers, TumorCollagen

Identifiers

PMID26040322
PMCPMC4485361
OpenAlexW2119063676

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.