Farnesyltransferase inhibitors as radiation sensitizers.

Activation of Ras, by mutation, overexpression, or by signaling through tyrosine kinase receptors, is associated with radioresistance. Thus, therapies that inhibit Ras function could be an effective means to radiosensitize selected types of solid tumors. Inhibition of Ras prenylation using a variety...

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Bibliografski detalji
Glavni autori: Mckenna, W, Muschel, R, Gupta, A, Hahn, S, Bernhard, E
Format: Journal article
Jezik:English
Izdano: 2002
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author Mckenna, W
Muschel, R
Gupta, A
Hahn, S
Bernhard, E
author_facet Mckenna, W
Muschel, R
Gupta, A
Hahn, S
Bernhard, E
author_sort Mckenna, W
collection OXFORD
description Activation of Ras, by mutation, overexpression, or by signaling through tyrosine kinase receptors, is associated with radioresistance. Thus, therapies that inhibit Ras function could be an effective means to radiosensitize selected types of solid tumors. Inhibition of Ras prenylation using a variety of farnesyltransferase inhibitors resulted in radiosensitization of tumor cells that expressed activated Ras, both in vitro and in xenograft models. Farnesyltransferase inhibitor treatment could also inhibit tumor regrowth following irradiation of mice bearing T24 tumor xenografts that express activated Ras. In a phase I trial of the farnesyltransferase inhibitor L-778-123 and radiotherapy in patients with locally advanced head and neck cancer and non-small cell lung cancer, a high response rate was observed coupled with a mild toxicity profile. Additional clinical trials should shed light on the potential of this and other farnesyltransferase inhibitors to serve as radiosensitizers and may identify molecular markers that could predict a response to these agents.
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spelling oxford-uuid:fc95a2a8-f402-4f3d-9d9b-b57aa0aae0352022-03-27T13:21:56ZFarnesyltransferase inhibitors as radiation sensitizers.Journal articlehttp://purl.org/coar/resource_type/c_dcae04bcuuid:fc95a2a8-f402-4f3d-9d9b-b57aa0aae035EnglishSymplectic Elements at Oxford2002Mckenna, WMuschel, RGupta, AHahn, SBernhard, EActivation of Ras, by mutation, overexpression, or by signaling through tyrosine kinase receptors, is associated with radioresistance. Thus, therapies that inhibit Ras function could be an effective means to radiosensitize selected types of solid tumors. Inhibition of Ras prenylation using a variety of farnesyltransferase inhibitors resulted in radiosensitization of tumor cells that expressed activated Ras, both in vitro and in xenograft models. Farnesyltransferase inhibitor treatment could also inhibit tumor regrowth following irradiation of mice bearing T24 tumor xenografts that express activated Ras. In a phase I trial of the farnesyltransferase inhibitor L-778-123 and radiotherapy in patients with locally advanced head and neck cancer and non-small cell lung cancer, a high response rate was observed coupled with a mild toxicity profile. Additional clinical trials should shed light on the potential of this and other farnesyltransferase inhibitors to serve as radiosensitizers and may identify molecular markers that could predict a response to these agents.
spellingShingle Mckenna, W
Muschel, R
Gupta, A
Hahn, S
Bernhard, E
Farnesyltransferase inhibitors as radiation sensitizers.
title Farnesyltransferase inhibitors as radiation sensitizers.
title_full Farnesyltransferase inhibitors as radiation sensitizers.
title_fullStr Farnesyltransferase inhibitors as radiation sensitizers.
title_full_unstemmed Farnesyltransferase inhibitors as radiation sensitizers.
title_short Farnesyltransferase inhibitors as radiation sensitizers.
title_sort farnesyltransferase inhibitors as radiation sensitizers
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AT hahns farnesyltransferaseinhibitorsasradiationsensitizers
AT bernharde farnesyltransferaseinhibitorsasradiationsensitizers