Evidence map›Paper›PMID 34761350›Full record

ReviewHuman cell2022

3D modeling in cancer studies.

Oula El Atat, Zahra Farzaneh, Mahsa Pourhamzeh, Fatima Taki, Ralph Abi-Habib, Massoud Vosough, Mirvat El-Sibai

Abstract readReview
PubMed Publisher
In one paragraph

Review in Human cell, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 37 papers.

0numbers the graph read from it
0cells of the map it votes in
37citing papers in PubMed
–field-weighted citation impact
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

37 citing papers in PubMed.

  1. Review
  2. Article
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  9. Review
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  14. Active fraction of ground cherry (Biomedical reports · 2024
    Article
  15. Article
  16. Review
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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.

Oula El Atat *Department of Natural Sciences, Lebanese American University, Beirut, Lebanon.
Zahra Farzaneh *Department of Regenerative Medicine, Cell Science Research Center, Royan Institute for Stem Cell Biology and Technology, ACECR, Tehran, Iran.
Mahsa Pourhamzeh *Department of Regenerative Medicine, Cell Science Research Center, Royan Institute for Stem Cell Biology and Technology, ACECR, Tehran, Iran.
Fatima TakiDepartment of Natural Sciences, Lebanese American University, Beirut, Lebanon.
Ralph Abi-HabibDepartment of Natural Sciences, Lebanese American University, Beirut, Lebanon.
Massoud VosoughDepartment of Regenerative Medicine, Cell Science Research Center, Royan Institute for Stem Cell Biology and Technology, ACECR, Tehran, Iran. masvos@Royaninstitute.org.
Mirvat El-SibaiDepartment of Natural Sciences, Lebanese American University, Beirut, Lebanon. mirvat.elsibai@lau.edu.lb.ORCID http://orcid.org/0000-0003-4084-6759

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The tumor microenvironment contributes significantly to tumor initiation, progression, and resistance to chemotherapy. Much of our understanding of the tumor and its microenvironment is developed using various methods of cell culture. Throughout the last two decades, research has increasingly shown that 3D cell culture systems can remarkably recapitulate the complexity of tumor architecture and physiology compared to traditional 2D models. Unlike the flat culture system, these novel models enabled more cell-cell and cell-extracellular matrix interactions. By mimicking in vivo microenvironment, 3D culture systems promise to become accurate tools ready to be used in diagnosis, drug screening, and personalized medicine. In this review, we discussed the importance of 3D culture in simulating the tumor microenvironment and focused on the effects of cancer cell-microenvironment interactions on cancer behavior, resistance, proliferation, and metastasis. Finally, we assessed the role of 3D cell culture systems in the contexts of drug screening. 2D culture system is used to study cancer cell growth, progression, behavior, and drug response. It provides contact between cells and supports paracrine crosstalk between host cells and cancer cells. However, this system fails to simulate the architecture and the physiological aspects of in vivo tumor microenvironment due to the absence of cell-cell/ cell-ECM interactions as well as unlimited access to O

Indexed as

Tumor MicroenvironmentAntineoplastic AgentsCell CommunicationCell Culture Techniques, Three DimensionalCell ProliferationDisease ProgressionDrug Resistance, NeoplasmDrug Screening Assays, AntitumorExtracellular MatrixHumansNeoplasmsTumor Cells, CulturedAntineoplastic Agents3D culture systemCancer cellsCell–cell interactionCell–extracellular matrix interactionModeling cancer organoids

Identifiers

What Socratic holds

Textmetadata
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 Socratic graph.