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Identification of proteasomal catalytic subunit PSMA6 as a therapeutic target for lung cancer

To identify potential therapeutic targets for lung cancer, we performed semi‐genome‐wide shRNA screening combined with the utilization of genome‐wide expression and copy number data. shRNA screening targeting 5043 genes in NCI‐H460 identified 51 genes as candidates. Pathway analysis revealed that th...

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Autores principales: Kakumu, Tomohiko, Sato, Mitsuo, Goto, Daiki, Kato, Toshio, Yogo, Naoyuki, Hase, Tetsunari, Morise, Masahiro, Fukui, Takayuki, Yokoi, Kohei, Sekido, Yoshitaka, Girard, Luc, Minna, John D., Byers, Lauren A., Heymach, John V., Coombes, Kevin R., Kondo, Masashi, Hasegawa, Yoshinori
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5406588/
https://www.ncbi.nlm.nih.gov/pubmed/28165654
http://dx.doi.org/10.1111/cas.13185
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author Kakumu, Tomohiko
Sato, Mitsuo
Goto, Daiki
Kato, Toshio
Yogo, Naoyuki
Hase, Tetsunari
Morise, Masahiro
Fukui, Takayuki
Yokoi, Kohei
Sekido, Yoshitaka
Girard, Luc
Minna, John D.
Byers, Lauren A.
Heymach, John V.
Coombes, Kevin R.
Kondo, Masashi
Hasegawa, Yoshinori
author_facet Kakumu, Tomohiko
Sato, Mitsuo
Goto, Daiki
Kato, Toshio
Yogo, Naoyuki
Hase, Tetsunari
Morise, Masahiro
Fukui, Takayuki
Yokoi, Kohei
Sekido, Yoshitaka
Girard, Luc
Minna, John D.
Byers, Lauren A.
Heymach, John V.
Coombes, Kevin R.
Kondo, Masashi
Hasegawa, Yoshinori
author_sort Kakumu, Tomohiko
collection PubMed
description To identify potential therapeutic targets for lung cancer, we performed semi‐genome‐wide shRNA screening combined with the utilization of genome‐wide expression and copy number data. shRNA screening targeting 5043 genes in NCI‐H460 identified 51 genes as candidates. Pathway analysis revealed that the 51 genes were enriched for the five pathways, including ribosome, proteasome, RNA polymerase, pyrimidine metabolism and spliceosome pathways. We focused on the proteasome pathway that involved six candidate genes because its activation has been demonstrated in diverse human malignancies, including lung cancer. Microarray expression and array CGH data showed that PSMA6, a proteasomal subunit of a 20S catalytic core complex, was highly expressed in lung cancer cell lines, with recurrent gene amplifications in some cases. Therefore, we further examined the roles of PSMA6 in lung cancer. Silencing of PSMA6 induced apoptosis or G2/M cell cycle arrest in cancer cell lines but not in an immortalized normal lung cell line. These results suggested that PSMA6 serves as an attractive target with a high therapeutic index for lung cancer.
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spelling pubmed-54065882017-05-01 Identification of proteasomal catalytic subunit PSMA6 as a therapeutic target for lung cancer Kakumu, Tomohiko Sato, Mitsuo Goto, Daiki Kato, Toshio Yogo, Naoyuki Hase, Tetsunari Morise, Masahiro Fukui, Takayuki Yokoi, Kohei Sekido, Yoshitaka Girard, Luc Minna, John D. Byers, Lauren A. Heymach, John V. Coombes, Kevin R. Kondo, Masashi Hasegawa, Yoshinori Cancer Sci Original Articles To identify potential therapeutic targets for lung cancer, we performed semi‐genome‐wide shRNA screening combined with the utilization of genome‐wide expression and copy number data. shRNA screening targeting 5043 genes in NCI‐H460 identified 51 genes as candidates. Pathway analysis revealed that the 51 genes were enriched for the five pathways, including ribosome, proteasome, RNA polymerase, pyrimidine metabolism and spliceosome pathways. We focused on the proteasome pathway that involved six candidate genes because its activation has been demonstrated in diverse human malignancies, including lung cancer. Microarray expression and array CGH data showed that PSMA6, a proteasomal subunit of a 20S catalytic core complex, was highly expressed in lung cancer cell lines, with recurrent gene amplifications in some cases. Therefore, we further examined the roles of PSMA6 in lung cancer. Silencing of PSMA6 induced apoptosis or G2/M cell cycle arrest in cancer cell lines but not in an immortalized normal lung cell line. These results suggested that PSMA6 serves as an attractive target with a high therapeutic index for lung cancer. John Wiley and Sons Inc. 2017-04-25 2017-04 /pmc/articles/PMC5406588/ /pubmed/28165654 http://dx.doi.org/10.1111/cas.13185 Text en © 2017 The Authors. Cancer Science published by John Wiley & Sons Australia, Ltd on behalf of Japanese Cancer Association. This is an open access article under the terms of the Creative Commons Attribution‐NonCommercial‐NoDerivs (http://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Original Articles
Kakumu, Tomohiko
Sato, Mitsuo
Goto, Daiki
Kato, Toshio
Yogo, Naoyuki
Hase, Tetsunari
Morise, Masahiro
Fukui, Takayuki
Yokoi, Kohei
Sekido, Yoshitaka
Girard, Luc
Minna, John D.
Byers, Lauren A.
Heymach, John V.
Coombes, Kevin R.
Kondo, Masashi
Hasegawa, Yoshinori
Identification of proteasomal catalytic subunit PSMA6 as a therapeutic target for lung cancer
title Identification of proteasomal catalytic subunit PSMA6 as a therapeutic target for lung cancer
title_full Identification of proteasomal catalytic subunit PSMA6 as a therapeutic target for lung cancer
title_fullStr Identification of proteasomal catalytic subunit PSMA6 as a therapeutic target for lung cancer
title_full_unstemmed Identification of proteasomal catalytic subunit PSMA6 as a therapeutic target for lung cancer
title_short Identification of proteasomal catalytic subunit PSMA6 as a therapeutic target for lung cancer
title_sort identification of proteasomal catalytic subunit psma6 as a therapeutic target for lung cancer
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5406588/
https://www.ncbi.nlm.nih.gov/pubmed/28165654
http://dx.doi.org/10.1111/cas.13185
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