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Radiosensitization by a novel Bcl-2 and Bcl-XL inhibitor S44563 in small-cell lung cancer

Radiotherapy has a critical role in the treatment of small-cell lung cancer (SCLC). The effectiveness of radiation in SCLC remains limited as resistance results from defects in apoptosis. In the current study, we investigated whether using the Bcl-2/Bcl-X L inhibitor S44563 can enhance radiosensitiv...

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Published in:Cell death & disease 2014-09, Vol.5 (9), p.e1423-e1423
Main Authors: Loriot, Y, Mordant, P, Dugue, D, Geneste, O, Gombos, A, Opolon, P, Guegan, J, Perfettini, J-L, Pierre, A, Berthier, L K, Kroemer, G, Soria, J C, Depil, S, Deutsch, E
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cited_by cdi_FETCH-LOGICAL-c4075-d24835c53f7b552eb96b51c1d91197a1e8037f5ac5e4d6a2f20e042bbac501f83
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creator Loriot, Y
Mordant, P
Dugue, D
Geneste, O
Gombos, A
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Pierre, A
Berthier, L K
Kroemer, G
Soria, J C
Depil, S
Deutsch, E
description Radiotherapy has a critical role in the treatment of small-cell lung cancer (SCLC). The effectiveness of radiation in SCLC remains limited as resistance results from defects in apoptosis. In the current study, we investigated whether using the Bcl-2/Bcl-X L inhibitor S44563 can enhance radiosensitivity of SCLC cells in vitro and in vivo . In vitro studies confirmed that S44563 caused SCLC cells to acquire hallmarks of apoptosis. S44563 markedly enhanced the sensitivity of SCLC cells to radiation, as determined by a clonogenic assay. The combination of S44563 and cisplatin-based chemo-radiation showed a significant tumor growth delay and increased overall survival in mouse xenograft models. This positive interaction was greater when S44563 was given after the completion of the radiation, which might be explained by the radiation-induced overexpression of anti-apoptotic proteins secondary to activation of the NF- κ B pathway. These data underline the possibility of combining IR and Bcl-2/Bcl-X L inhibition in the treatment of SCLC as they underscore the importance of administering conventional and targeted therapies in an optimal sequence.
doi_str_mv 10.1038/cddis.2014.365
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subjects 631/67/1059/485
631/67/1059/99
631/67/1612/2143
631/80/82/23
Animals
Antibodies
Apoptosis - drug effects
Apoptosis - radiation effects
bcl-X Protein - antagonists & inhibitors
bcl-X Protein - genetics
bcl-X Protein - metabolism
Biochemistry
Biomedical and Life Sciences
Cell Biology
Cell Culture
Cell Proliferation - drug effects
Cell Proliferation - radiation effects
Cisplatin - administration & dosage
Combined Modality Therapy
Female
Heterocyclic Compounds, 3-Ring - administration & dosage
Humans
Immunology
Life Sciences
Lung cancer
Lung Neoplasms - drug therapy
Lung Neoplasms - genetics
Lung Neoplasms - metabolism
Lung Neoplasms - radiotherapy
Mice
Mice, Nude
NF-kappa B - genetics
NF-kappa B - metabolism
Original
original-article
Proto-Oncogene Proteins c-bcl-2 - antagonists & inhibitors
Proto-Oncogene Proteins c-bcl-2 - genetics
Proto-Oncogene Proteins c-bcl-2 - metabolism
Radiation Tolerance
Radiation-Sensitizing Agents - administration & dosage
Small Cell Lung Carcinoma - drug therapy
Small Cell Lung Carcinoma - genetics
Small Cell Lung Carcinoma - metabolism
Small Cell Lung Carcinoma - radiotherapy
Sulfonamides - administration & dosage
Xenograft Model Antitumor Assays
title Radiosensitization by a novel Bcl-2 and Bcl-XL inhibitor S44563 in small-cell lung cancer
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