Evidence map›Paper›PMID 31873199›Full record

ArticleScientific reports2019

A 3D Printed Hanging Drop Dripper for Tumor Spheroids Analysis Without Recovery.

Liang Zhao, Jidong Xiu, Yang Liu, Tianye Zhang, Wenjie Pan, Xiaonan Zheng, Xueji Zhang

Abstract read
In one paragraph

Article in Scientific reports, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 50 papers.

0numbers the graph read from it
0cells of the map it votes in
50citing 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

50 citing papers in PubMed.

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  11. Principles of Hanging Drop Method (Spheroid Formation) in Cell Culture.Methods in molecular biology (Clifton, N.J.) · 2025
    Article
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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.

Liang ZhaoInstitute of Precision Medicine and Health, University of Science and Technology Beijing, Beijing, 100083, China. zhaoliang2013@ustb.edu.cn.ORCID http://orcid.org/0000-0001-6273-2651
Jidong XiuInstitute of Precision Medicine and Health, University of Science and Technology Beijing, Beijing, 100083, China.
Yang LiuInstitute of Precision Medicine and Health, University of Science and Technology Beijing, Beijing, 100083, China.
Tianye ZhangInstitute of Precision Medicine and Health, University of Science and Technology Beijing, Beijing, 100083, China.
Wenjie PanInstitute of Precision Medicine and Health, University of Science and Technology Beijing, Beijing, 100083, China.
Xiaonan ZhengInstitute of Precision Medicine and Health, University of Science and Technology Beijing, Beijing, 100083, China.
Xueji ZhangInstitute of Precision Medicine and Health, University of Science and Technology Beijing, Beijing, 100083, China. zhangxueji@ustb.edu.cn.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Compared with traditional monolayer cell culture, the three-dimensional tumor spheroid has emerged as an essential in vitro model for cancer research due to the recapitulation of the architecture and physiology of solid human tumors. Herein, by implementing the rapid prototyping of a benchtop 3D printer, we developed a new strategy to generate and analyze tumor spheroids on a commonly used multi-well plate. In this method, the printed artifact can be directly mounted on a 96/384-well plate, enables hanging drop-based spheroid formation, avoiding the tedious fabrication process from micromechanical systems. Besides long-term spheroid culture (20 days), this method supports subsequent analysis of tumor spheroid by seamlessly dripping from the printed array, thereby eliminating the need for spheroids retrieval for downstream characterization. We demonstrated several tumor spheroid-based assays, including tumoroid drug testing, metastasis on or inside extracellular matrix gel, and tumor transendothelial (TEM) assay. Based on quantitative phenotypical and molecular analysis without any precarious retrieval and transfer, we found that the malignant breast cancer (MDA-MB-231) cell aggregate presents a more metastatic morphological phenotype than the non-malignant breast cancer (MCF-7) and colonial cancer (HCT-116) cell spheroid, and shows an up-regulation of epithelial-mesenchymal transition (EMT) relevant genes (fold change > 2). Finally, we validated this tumor malignancy by the TEM assay, which could be easily performed using our approach. This methodology could provide a useful workflow for expediting tumoroid modeled in vitro assay, allowing the "Lab-on-a-Cloud" scenario for routine study.

Indexed as

Printing, Three-DimensionalCell Line, TumorDrug Resistance, NeoplasmHumansNeoplasm InvasivenessNeoplasmsSpheroids, CellularTransendothelial and Transepithelial Migration

Identifiers

PMID31873199
PMCPMC6928160

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.