Evidence map›Paper›PMID 32178458›Full record

ArticleInternational journal of molecular sciences2020

Humanization of Tumor Stroma by Tissue Engineering as a Tool to Improve Squamous Cell Carcinoma Xenograft.

Sara Guerrero-Aspizua, Andrea González-Masa, Claudio J Conti, Marta García, Esteban Chacón-Solano, Fernando Larcher, Marcela Del Río

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2020. 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
0.8field-weighted citation impact, top 28% 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

6 citing papers in PubMed, 7 citations in OpenAlex.

  1. Collagen remodeling in breast cancer progression: from molecular mechanisms to diagnostic and therapeutic opportunities.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2026
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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 at 3 institutions in 1 country.

Sara Guerrero-AspizuaDepartment of Bioengineering, Universidad Carlos III de Madrid, 28911 Leganés, Spain.
Andrea González-MasaDepartment of Bioengineering, Universidad Carlos III de Madrid, 28911 Leganés, Spain.
Claudio J ContiDepartment of Bioengineering, Universidad Carlos III de Madrid, 28911 Leganés, Spain.
Marta GarcíaDepartment of Bioengineering, Universidad Carlos III de Madrid, 28911 Leganés, Spain.
Esteban Chacón-SolanoDepartment of Bioengineering, Universidad Carlos III de Madrid, 28911 Leganés, Spain.
Fernando LarcherDepartment of Bioengineering, Universidad Carlos III de Madrid, 28911 Leganés, Spain.
Marcela Del RíoDepartment of Bioengineering, Universidad Carlos III de Madrid, 28911 Leganés, Spain.
Centre for Biomedical Network Research on Rare Diseases · ESHospital Universitario Fundación Jiménez Díaz · ESUniversidad Carlos III de Madrid · ES

Funding

Comunidad de Madrid B2017/BMD-3692DEBRA International HEALTH-F2-2011-261392Instituto de Salud Carlos III PI17/01747Ministerio de Ciencia e Innovación SAF2017-86810-R
6 · The paper itself

Abstract

The role of stroma is fundamental in the development and behavior of epithelial tumors. In this regard, limited growth of squamous cell carcinomas (SCC) or cell-lines derived from them has been achieved in immunodeficient mice. Moreover, lack of faithful recapitulation of the original human neoplasia complexity is often observed in xenografted tumors. Here, we used tissue engineering techniques to recreate a humanized tumor stroma for SCCs grafted in host mice, by combining CAF (cancer associated fibroblasts)-like cells with a biocompatible scaffold. The stroma was either co-injected with epithelial cell lines derived from aggressive SCC or implanted 15 days before the injection of the tumoral cells, to allow its vascularization and maturation. None of the mice injected with the cell lines without stroma were able to develop a SCC. In contrast, tumors were able to grow when SCC cells were injected into previously established humanized stroma. Histologically, all of the regenerated tumors were moderately differentiated SCC with a well-developed stroma, resembling that found in the original human neoplasm. Persistence of human stromal cells was also confirmed by immunohistochemistry. In summary, we provide a proof of concept that humanized tumor stroma, generated by tissue engineering, can facilitate the development of epithelial tumors in immunodeficient mice.

Indexed as

AnimalsCancer-Associated FibroblastsCarcinoma, Squamous CellCell LineCell Line, TumorEpithelial CellsFemaleFibroblastsHeterograftsHumansMiceNeoplasm TransplantationNeovascularization, PathologicStromal CellsTissue EngineeringTransplantation, HeterologousCAFSCCstromatissue engineeringtumorxenografts

Identifiers

PMID32178458
PMCPMC7139348
OpenAlexW3012034805

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.