Evidence map›Paper›PMID 30056557›Full record

ReviewJournal of mammary gland biology and neoplasia2019

In Vitro Models for Studying Invasive Transitions of Ductal Carcinoma In Situ.

Ethan J Brock, Kyungmin Ji, Seema Shah, Raymond R Mattingly, Bonnie F Sloane

Abstract readReview
In one paragraph

Review in Journal of mammary gland biology and neoplasia, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
2.3field-weighted citation impact, top 9% 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

22 citing papers in PubMed, 40 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
  4. Article
  5. Article
  6. Review
  7. Article
  8. Review
  9. Review
  10. Ductal Carcinoma in Situ: Molecular Changes Accompanying Disease Progression.Journal of mammary gland biology and neoplasia · 2022
    Review
  11. Article
  12. Mechanical Studies of the Third Dimension in Cancer: From 2D to 3D Model.International journal of molecular sciences · 2021
    Review
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Modeling chemical effects on breast cancer: the importance of the microenvironment in vitro.Integrative biology : quantitative biosciences from nano to macro · 2020
    Review
  20. 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

5 authors at 1 institution in 1 country.

Ethan J BrockProgram in Cancer Biology, Wayne State University School of Medicine, Detroit, MI, 48201, USA.
Kyungmin JiDepartment of Pharmacology, Wayne State University School of Medicine, Detroit, MI, 48201, USA.
Seema ShahProgram in Cancer Biology, Wayne State University School of Medicine, Detroit, MI, 48201, USA.
Raymond R MattinglyProgram in Cancer Biology, Wayne State University School of Medicine, Detroit, MI, 48201, USA.
Bonnie F SloaneProgram in Cancer Biology, Wayne State University School of Medicine, Detroit, MI, 48201, USA. bsloane@med.wayne.edu.ORCID 0000-0001-6833-9615
Wayne State University · US

Funding

Tumor Biology and Microenvironment (Program 1)P30CA022453 · NCI · WAYNE STATE UNIVERSITY · PI Julie Lynn Boerner · 1985 to 2026
$68.4M
RESEARCH CORE-- SIGNAL TRANSDUCTIONP30ES006639 · NIEHS · WAYNE STATE UNIVERSITY · PI RUNGE-MORRIS, MELISSA A · 1994 to 2008
$13.1M
"Research Supplement to Promote Diversity in Health-Related Research", as part of Moffitt PS-OC, "Cancer as a Complex adaptive System"U54CA193489 · NCI · H. LEE MOFFITT CANCER CTR & RES INST · PI ANDERSON, ALEXANDER ROBERTSON ALLAN, GATENBY, ROBERT A · 2015 to 2020
$12.5M
TRAINING PROGRAM IN THE BIOLOGY OF CANCERT32CA009531 · NCI · WAYNE STATE UNIVERSITY · PI Larry H Matherly · 1985 to 2026
$5.3M
Proteolytic Pathways in Progression of Pre-Malignant Breast DiseaseR01CA131990 · NCI · WAYNE STATE UNIVERSITY · PI MATTINGLY, RAYMOND R, SLOANE, BONNIE F · 2008 to 2013
$1.9M
4D Microfluidic Platforms for Targeting Breast Cancer:Lymphatic InteractionsR21CA175931 · NCI · WAYNE STATE UNIVERSITY · PI SLOANE, BONNIE F · 2013 to 2014
$359k
Sprouty4 is a negative regulator of ERK/MAPK signaling in breast cancer and plays a role in the transition from in situ to invasive diseaseF31CA213807 · NCI · WAYNE STATE UNIVERSITY · PI BROCK, ETHAN J · 2017 to 2019
$123k
NCI NIH HHS F31 CA213807NCI NIH HHS P30 CA022453NCI NIH HHS R01 CA131990NCI NIH HHS R21 CA175931NCI NIH HHS T32 CA009531NCI NIH HHS U54 CA193489NIEHS NIH HHS P30 ES006639NIH HHS F31 CA213807NIH HHS P30 CA22453NIH HHS R01 CA131990NIH HHS R21 CA175931NIH HHS T32 CA009531NIH HHS U54 CA193489
6 · The paper itself

Abstract

About one fourth of all newly identified cases of breast carcinoma are diagnoses of breast ductal carcinoma in situ (DCIS). Since we cannot yet distinguish DCIS cases that would remain indolent from those that may progress to life-threatening invasive ductal carcinoma (IDC), almost all women undergo aggressive treatment. In order to allow for more rational individualized treatment, we and others are developing in vitro models to identify and validate druggable pathways that mediate the transition of DCIS to IDC. These models range from conventional two-dimensional (2D) monolayer cultures on plastic to 3D cultures in natural or synthetic matrices. Some models consist solely of DCIS cells, either cell lines or primary cells. Others are co-cultures that include additional cell types present in the normal or cancerous human breast. The 3D co-culture models more accurately mimic structural and functional changes in breast architecture that accompany the transition of DCIS to IDC. Mechanistic studies of the dynamic and temporal changes associated with this transition are facilitated by adapting the in vitro models to engineered microfluidic platforms. Ultimately, the goal is to create in vitro models that can serve as a reproducible preclinical screen for testing therapeutic strategies that will reduce progression of DCIS to IDC. This review will discuss the in vitro models that are currently available, as well as the progress that has been made using them to understand DCIS pathobiology.

Indexed as

BreastBreast NeoplasmsCarcinoma, Ductal, BreastCarcinoma, Intraductal, NoninfiltratingCell Line, TumorCoculture TechniquesDrug Screening Assays, AntitumorFemaleHumansNeoplasm InvasivenessPrimary Cell Culture2D cultures3D culturesCo-culturesEngineered microfluidic platformsNatural matricesPreclinical screensSynthetic matricesTumor microenvironment

Identifiers

PMID30056557
PMCPMC6641861
OpenAlexW2884516513

What OpenQuestion holds

Textmetadata
LicenceTDM
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.