» Articles » PMID: 32276468

Time- and Dose-Dependent Effects of Ionizing Irradiation on the Membrane Expression of Hsp70 on Glioma Cells

Overview
Journal Cells
Publisher MDPI
Date 2020 Apr 12
PMID 32276468
Citations 7
Authors
Affiliations
Soon will be listed here.
Abstract

The major stress-inducible protein Hsp70 (HSPA1A) is overexpressed in the cytosol of many highly aggressive tumor cells including glioblastoma multiforme and presented on their plasma membrane. Depending on its intracellular or membrane localization, Hsp70 either promotes tumor growth or serves as a target for natural killer (NK) cells. The kinetics of the membrane Hsp70 (mHsp70) density on human glioma cells (U87) was studied after different irradiation doses to define the optimal therapeutic window for Hsp70-targeting NK cells. To maintain the cells in the exponential growth phase during a cultivation period of 7 days, different initial cell counts were seeded. Although cytosolic Hsp70 levels remained unchanged on days 4 and 7 after a sublethal irradiation with 2, 4 and 6 Gy, a dose of 2 Gy resulted in an upregulated mHsp70 density in U87 cells which peaked on day 4 and started to decline on day 7. Higher radiation doses (4 Gy, 6 Gy) resulted in an earlier and more rapid onset of the mHsp70 expression on days 2 and 1, respectively, followed by a decline on day 5. Membrane Hsp70 levels were higher on cells in G2/M than in G1; however, an irradiation-induced cell cycle arrest on days 4 and 7 was not associated with an increase in the mHsp70 density. Extracellular Hsp70 concentrations in the supernatant of irradiated cells were significantly higher than sham (0 Gy) irradiated cells on days 4 and 7, but not on day 1. Functionally, elevated mHsp70 densities were associated with a significantly better lysis by Hsp70-targeting NK cells. In summary, the kinetics of changes in the mHsp70 density upon irradiation on tumor cells is time- and dose-dependent.

Citing Articles

Membrane-bound Heat Shock Protein mHsp70 Is Required for Migration and Invasion of Brain Tumors.

Shevtsov M, Bobkov D, Yudintceva N, Likhomanova R, Kim A, Fedorov E Cancer Res Commun. 2024; 4(8):2025-2044.

PMID: 39015084 PMC: 11317918. DOI: 10.1158/2767-9764.CRC-24-0094.


The radiation- and chemo-sensitizing capacity of diclofenac can be predicted by a decreased lactate metabolism and stress response.

Schwab M, Bashiri Dezfouli A, Khosravi M, Alkotub B, Bauer L, Birgani M Radiat Oncol. 2024; 19(1):7.

PMID: 38229111 PMC: 10790495. DOI: 10.1186/s13014-024-02399-5.


Anti-GD2 Antibody Dinutuximab Beta and Low-Dose Interleukin 2 After Haploidentical Stem-Cell Transplantation in Patients With Relapsed Neuroblastoma: A Multicenter, Phase I/II Trial.

Flaadt T, Ladenstein R, Ebinger M, Lode H, Arnardottir H, Poetschger U J Clin Oncol. 2023; 41(17):3135-3148.

PMID: 36854071 PMC: 10256422. DOI: 10.1200/JCO.22.01630.


Combined Cytotoxic Effect of Inhibitors of Proteostasis on Human Colon Cancer Cells.

Nikotina A, Vladimirova S, Kokoreva N, Komarova E, Aksenov N, Efremov S Pharmaceuticals (Basel). 2022; 15(8).

PMID: 35893747 PMC: 9331496. DOI: 10.3390/ph15080923.


Phosphatidylinositol Monophosphates Regulate the Membrane Localization of HSPA1A, a Stress-Inducible 70-kDa Heat Shock Protein.

Smulders L, Altman R, Briseno C, Saatchi A, Wallace L, AlSebaye M Biomolecules. 2022; 12(6).

PMID: 35740982 PMC: 9221345. DOI: 10.3390/biom12060856.


References
1.
Thorsteinsdottir J, Stangl S, Fu P, Guo K, Albrecht V, Eigenbrod S . Overexpression of cytosolic, plasma membrane bound and extracellular heat shock protein 70 (Hsp70) in primary glioblastomas. J Neurooncol. 2017; 135(3):443-452. DOI: 10.1007/s11060-017-2600-z. View

2.
Kokowski K, Stangl S, Seier S, Hildebrandt M, Vaupel P, Multhoff G . Radiochemotherapy combined with NK cell transfer followed by second-line PD-1 inhibition in a patient with NSCLC stage IIIb inducing long-term tumor control: a case study. Strahlenther Onkol. 2019; 195(4):352-361. PMC: 6433810. DOI: 10.1007/s00066-019-01434-9. View

3.
Pasi F, Paolini A, Nano R, Liberto R, Capelli E . Effects of single or combined treatments with radiation and chemotherapy on survival and danger signals expression in glioblastoma cell lines. Biomed Res Int. 2014; 2014:453497. PMC: 4100347. DOI: 10.1155/2014/453497. View

4.
Gehrmann M, Liebisch G, Schmitz G, Anderson R, Steinem C, De Maio A . Tumor-specific Hsp70 plasma membrane localization is enabled by the glycosphingolipid Gb3. PLoS One. 2008; 3(4):e1925. PMC: 2271151. DOI: 10.1371/journal.pone.0001925. View

5.
Gross C, Koelch W, DeMaio A, Arispe N, Multhoff G . Cell surface-bound heat shock protein 70 (Hsp70) mediates perforin-independent apoptosis by specific binding and uptake of granzyme B. J Biol Chem. 2003; 278(42):41173-81. DOI: 10.1074/jbc.M302644200. View