Tumour relapse is believed to be caused by rare cancer-cells with stem-cell properties (cancer stem cells) that are intrinsically resistant to available treatments. The identification of novel strategies to increase their sensitivity has major clinical implications. Latest clinical trials have shown a positive antitumoral effect of hyperthermia in combination with chemotherapy or radiotherapy. In a recent paper, the combination of increased temperature at the tumour site, generated by laser treatment of intravenously-injected gold nanoshells, and ionizing radiations enhances radiosensitivity of cancer stem cells and tumor response. At the root of the success of hyperthermia in enhancing radio-sensitization of cancer stem cells is the inhibition of their capacity to repair DNA damage, affecting the survival rate of these cells.

Heating cancer stem cells to reduce tumor relapse / PG. Pelicci, P. Dalton, R. Orecchia. - In: BREAST CANCER RESEARCH. - ISSN 1465-5411. - 13:3(2011 May 06), p. 305.

Heating cancer stem cells to reduce tumor relapse

PG. Pelicci
Primo
;
R. Orecchia
Ultimo
2011

Abstract

Tumour relapse is believed to be caused by rare cancer-cells with stem-cell properties (cancer stem cells) that are intrinsically resistant to available treatments. The identification of novel strategies to increase their sensitivity has major clinical implications. Latest clinical trials have shown a positive antitumoral effect of hyperthermia in combination with chemotherapy or radiotherapy. In a recent paper, the combination of increased temperature at the tumour site, generated by laser treatment of intravenously-injected gold nanoshells, and ionizing radiations enhances radiosensitivity of cancer stem cells and tumor response. At the root of the success of hyperthermia in enhancing radio-sensitization of cancer stem cells is the inhibition of their capacity to repair DNA damage, affecting the survival rate of these cells.
Settore MED/04 - Patologia Generale
Settore MED/36 - Diagnostica per Immagini e Radioterapia
6-mag-2011
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2434/164805
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