Evidence map›Paper›PMID 35908685›Full record

ReviewDrug discovery today2022

How to build a tumor: An industry perspective.

Julia Schueler, Jeffrey Borenstein, Ludoviko Buti, Meng Dong, Fatma Masmoudi, Kolin Hribar, Elizabeth Anderson, Wolfgang Sommergruber

Abstract readReview
In one paragraph

Review in Drug discovery today, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 citing papers in PubMed.

  1. Review
  2. Review
  3. Breaking the mold: 3D cell cultures reshaping the future of cancer research.Frontiers in cell and developmental biology · 2024
    Review
  4. Review
  5. Review
  6. 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

8 authors.

Julia SchuelerCharles River Discovery Research Services Germany GmbH, Freiburg, Germany. Electronic address: julia.schueler@crl.com.
Jeffrey BorensteinBioengineering Division, Draper, Cambridge, MA, USA.
Ludoviko ButiCharles River Discovery, Leiden, the Netherlands.
Meng DongDr Margarete Fischer-Bosch Institute of Clinical Pharmacology and University of Tuebingen, Stuttgart, Germany.
Fatma MasmoudiCharles River Discovery, Leiden, the Netherlands.
Kolin HribarCypre, South San Francisco, CA, USA.
Elizabeth AndersonCharles River, Saffron Walden, UK.
Wolfgang SommergruberUniversity of Applied Sciences, Department of Biotechnology, Vienna, Austria.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

During the past 15 years, a plethora of innovative 3D in vitro systems has been developed. They offer the possibility of identifying crucial cellular and molecular contributors to the disease by permitting manipulation of each in isolation. However, improvements are needed particularly with respect to the predictivity and validity of those models. The major challenge now is to identify which assay and readout combination(s) best suits the current scientific question(s). A deep understanding of the different platforms along with their pros and cons is a prerequisite to make this decision. This review aims to give an overview of the most prominent systems with a focus on applications, translational relevance and adoption drivers from an industry perspective.

Indexed as

NeoplasmsHumans3D in vitro modelsOncology drug developmentTechnology landscape

Identifiers

PMID35908685
PMCPMC9585375

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
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.