Tumor cell invasion into Matrigel: optimized protocol for RNA extraction

Author:

Ferretti Roberta1,Baldassarre Antonella2,Billy Emmanuel de1,M Carcaboso Angel3,Moore Andrew45,Carai Andrea6,Mastronuzzi Angela7,Masotti Andrea2ORCID,Vinci Maria1ORCID

Affiliation:

1. Department of Onco-haematology, Gene & Cell Therapy, Bambino Gesù Children’s Hospital-IRCCS, Rome, 00146, Italy

2. Multifactorial & Complex Phenotypes Research Area, Bambino Gesù Children’s Hospital-IRCCS, Rome, 00146, Italy

3. Developmental Tumor Biology Laboratory, Hospital Sant Joan de Déu, Barcelona, 08004, Spain

4. Oncology Service, Queensland Children’s Hospital, Brisbane, 4101, Australia

5. Child Health Research Centre, The University of Queensland, Brisbane, 4101, Australia

6. Oncological Neurosurgery Unit, Department of Neuroscience & Neurorehabilitation, Bambino Gesù Children’s Hospital-IRCCS, Rome, 00165, Italy

7. Neuro-oncology Unit, Department of Onco-hematology, Gene & Cell Therapy, Bambino Gesù Children’s Hospital-IRCCS, Rome, 00165, Italy

Abstract

3D models are increasingly used to study mechanisms driving tumor progression and mimicking in vitro processes such as invasion and migration. However, there is a need to establish more protocols based on 3D culture systems that allow for downstream molecular biology investigations. Materials & methods: Here we present a method for optimal RNA extraction from highly aggressive primary glioma cells invading into Matrigel. The method has been established by comparing previously reported protocols, available commercial kits and optimizing specific steps for matrix dissociation, RNA separation and purification. Results and conclusion: The protocol allows RNA extraction from cells embedded into Matrigel, with optimal yield, purity and integrity suitable for subsequent sequencing analysis of both high and low molecular weight RNA.

Funder

CHILDREN with CANCER UK

Publisher

Future Science Ltd

Subject

General Biochemistry, Genetics and Molecular Biology,Biotechnology

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