Evidence map›Paper›PMID 29881724›Full record

ReviewFrontiers in bioengineering and biotechnology2018

Engineering Breast Cancer Microenvironments and 3D Bioprinting.

Jorge A Belgodere, Connor T King, Jacob B Bursavich, Matthew E Burow, Elizabeth C Martin, Jangwook P Jung

Open access · goldAbstract readReview
In one paragraph

Review in Frontiers in bioengineering and biotechnology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 63 papers.

0numbers the graph read from it
0cells of the map it votes in
63citing papers in PubMed
6.6field-weighted citation impact, top 3% 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

63 citing papers in PubMed, 106 citations in OpenAlex.

  1. Review
  2. Article
  3. 3D bioprinting innovations: a new frontier in breast cancer research.Medical oncology (Northwood, London, England) · 2025
    Review
  4. Article
  5. Review
  6. Article
  7. Targeted Cancer Therapy-on-A-Chip.Advanced healthcare materials · 2024
    Review
  8. Review
  9. Review
  10. Review
  11. Review
  12. Review
  13. Biomaterial-basedCancer pathogenesis and therapy · 2023
    Review
  14. Review
  15. Review
  16. Article
  17. Review
  18. Review
  19. Article
  20. Article

3 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

6 authors at 2 institutions in 1 country.

Jorge A BelgodereDepartment of Biological and Agricultural Engineering, Louisiana State University, Baton Rouge, LA, United States.
Connor T KingDepartment of Biological and Agricultural Engineering, Louisiana State University, Baton Rouge, LA, United States.
Jacob B BursavichDepartment of Biological and Agricultural Engineering, Louisiana State University, Baton Rouge, LA, United States.
Matthew E BurowDepartment of Medicine, Section Hematology/Oncology, Tulane University, New Orleans, LA, United States.
Elizabeth C MartinDepartment of Biological and Agricultural Engineering, Louisiana State University, Baton Rouge, LA, United States.
Jangwook P JungDepartment of Biological and Agricultural Engineering, Louisiana State University, Baton Rouge, LA, United States.
Louisiana State University · USTulane University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The extracellular matrix (ECM) is a critical cue to direct tumorigenesis and metastasis. Although two-dimensional (2D) culture models have been widely employed to understand breast cancer microenvironments over the past several decades, the 2D models still exhibit limited success. Overwhelming evidence supports that three dimensional (3D), physiologically relevant culture models are required to better understand cancer progression and develop more effective treatment. Such platforms should include cancer-specific architectures, relevant physicochemical signals, stromal-cancer cell interactions, immune components, vascular components, and cell-ECM interactions found in patient tumors. This review briefly summarizes how cancer microenvironments (stromal component, cell-ECM interactions, and molecular modulators) are defined and what emerging technologies (perfusable scaffold, tumor stiffness, supporting cells within tumors and complex patterning) can be utilized to better mimic native-like breast cancer microenvironments. Furthermore, this review emphasizes biophysical properties that differ between primary tumor ECM and tissue sites of metastatic lesions with a focus on matrix modulation of cancer stem cells, providing a rationale for investigation of underexplored ECM proteins that could alter patient prognosis. To engineer breast cancer microenvironments, we categorized technologies into two groups: (1) biochemical factors modulating breast cancer cell-ECM interactions and (2) 3D bioprinting methods and its applications to model breast cancer microenvironments. Biochemical factors include matrix-associated proteins, soluble factors, ECMs, and synthetic biomaterials. For the application of 3D bioprinting, we discuss the transition of 2D patterning to 3D scaffolding with various bioprinting technologies to implement biophysical cues to model breast cancer microenvironments.

Indexed as

3D bioprintingbiophysical propertiescancer microenvironmentscell-ECM interactionsextracellular matrixtumor models

Identifiers

PMID29881724
PMCPMC5978274
OpenAlexW2801095534

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.