Evidence map›Paper›PMID 25856378›Full record

ArticlePloS one2015

In vitro microtumors provide a physiologically predictive tool for breast cancer therapeutic screening.

Gabriel Benton, Gerald DeGray, Hynda K Kleinman, Jay George, Irina Arnaoutova

Abstract read
In one paragraph

Article in PloS one, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing 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

32 citing papers in PubMed.

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  9. Matrigel: history/background, uses, and future applications.Journal of cell communication and signaling · 2022
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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

5 authors.

Gabriel BentonTrevigen Inc., Gaithersburg, MD, United States of America.
Gerald DeGrayTrevigen Inc., Gaithersburg, MD, United States of America.
Hynda K KleinmanTrevigen Inc., Gaithersburg, MD, United States of America.
Jay GeorgeTrevigen Inc., Gaithersburg, MD, United States of America.
Irina ArnaoutovaTrevigen Inc., Gaithersburg, MD, United States of America.

Funding

NCI NIH HHS HHSN261201300042CPHS HHS HHSN261201300042C
6 · The paper itself

Abstract

Many anti-cancer drugs fail in human trials despite showing efficacy in preclinical models. It is clear that the in vitro assays involving 2D monoculture do not reflect the complex extracellular matrix, chemical, and cellular microenvironment of the tumor tissue, and this may explain the failure of 2D models to predict clinical efficacy. We first optimized an in vitro microtumor model using a tumor-aligned ECM, a tumor-aligned medium, MCF-7 and MDA-MB-231 breast cancer spheroids, human umbilical vein endothelial cells, and human stromal cells to recapitulate the tissue architecture, chemical environment, and cellular organization of a growing and invading tumor. We assayed the microtumor for cell proliferation and invasion in a tumor-aligned extracellular matrix, exhibiting collagen deposition, acidity, glucose deprivation, and hypoxia. We found maximal proliferation and invasion when the multicellular spheroids were cultured in a tumor-aligned medium, having low pH and low glucose, with 10% fetal bovine serum under hypoxic conditions. In a 7-day assay, varying doses of fluorouracil or paclitaxel had differential effects on proliferation for MCF-7 and MDA-MB-231 tumor spheroids in microtumor compared to 2D and 3D monoculture. The microtumors exhibited a tumor morphology and drug response similar to published xenograft data, thus demonstrating a more physiologically predictive in vitro model.

Indexed as

In Vitro TechniquesBreast NeoplasmsCell HypoxiaCell ProliferationExtracellular MatrixFemaleHumansHuman Umbilical Vein Endothelial CellsMCF-7 CellsNeoplasm InvasivenessSpheroids, CellularTumor Microenvironment

Identifiers

PMID25856378
PMCPMC4391795

What OpenQuestion holds

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Registered trials

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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.