Role of HSP70 in response to (thermo)radiotherapy: analysis of gene expression in canine osteosarcoma cells by RNA-seq

Autor: Mathias S. Weyland, Carla Rohrer Bley, Pauline Thumser-Henner, Giancarlo Russo, Katarzyna J. Nytko
Přispěvatelé: University of Zurich, Nytko, Katarzyna J
Jazyk: angličtina
Rok vydání: 2020
Předmět:
Disease model
animal

10253 Department of Small Animals
Vesicular Transport Proteins
lcsh:Medicine
Bone neoplasm
615: Pharmakologie und Therapeutik
Membrane glycoprotein
Gene expression
Dog
Vesicular transport protein
Bone cancer
Cluster Analysis
RNA-Seq
11434 Center for Clinical Studies
RNA
Small Interfering

lcsh:Science
Cancer
Regulation of gene expression
Gene knockdown
Osteosarcoma
Principal Component Analysis
Multidisciplinary
Membrane Glycoproteins
HSP70 heat-shock protein
Transfection
Photon
Gene Expression Regulation
Neoplastic

Matrix Metalloproteinase 1
Hyperthermia
610 Medicine & health
Bone Neoplasms
Biology
Canine Osteosarcoma
Article
Dogs
medicine
Animals
HSP70 Heat-Shock Proteins
RNA
Messenger

Cell Proliferation
1000 Multidisciplinary
Photons
11077 Center for Applied Biotechnology and Molecular Medicine
Radiotherapy
Animal
572: Biochemie
Cell growth
lcsh:R
Hyperthermia
Induced

medicine.disease
Disease Models
Animal

Cancer research
lcsh:Q
Zdroj: Scientific Reports
Scientific Reports, 10 (1)
Scientific Reports, Vol 10, Iss 1, Pp 1-9 (2020)
ISSN: 2045-2322
Popis: Pre-treatment of tumors with hyperthermia is often used to increase the efficacy of radiotherapy. One of the main proteins induced in response to hyperthermia is heat shock protein 70 (HSP70). The aim of our study was to investigate up- and down-regulated genes in response to (thermo)radiotherapy in HSP70 proficient and deficient canine osteosarcoma cell line (Abrams), and functional role of HSP70 in the mechanism of thermoradiosensitization. Cells were transfected with negative control siRNA or siRNA targeting HSP70 and treated with hyperthermia (HT), radiotherapy (RT), and thermoradiotherapy (HTRT). RNA sequencing was used to analyze gene expression. Hyperthermia and thermoradiotherapy, but not radiotherapy alone, induced differential gene expression. We identified genes differentially expressed only in HSP70 knockdown (thus HSP70-dependent) cells in response to hyperthermia and thermoradiotherapy. Interestingly, cell proliferation but not clonogenicity and apoptosis/necrosis was affected by the HSP70 knockdown in response to thermoradiotherapy. The results suggest that HSP70 regulates expression of specific genes in response to hyperthermia and thermoradiotherapy. Further investigations into the role of specific genes regulated in a HSP70-dependent manner in response to thermoradiotherapy could pave a way into new, combinatorial treatment options for (canine) osteosarcoma and other cancer types.
Scientific Reports, 10 (1)
ISSN:2045-2322
Databáze: OpenAIRE