Cargando…

Inhibitor for protein disulfide-isomerase family A member 3 enhances the antiproliferative effect of inhibitor for mechanistic target of rapamycin in liver cancer: An in vitro study on combination treatment with everolimus and 16F16

mTOR is involved in the proliferation of liver cancer. However, the clinical benefit of treatment with mTOR inhibitors for liver cancer is controversial. Protein disulfide isomerase A member 3 (PDIA3) is a chaperone protein, and it supports the assembly of mTOR complex 1 (mTORC1) and stabilizes sign...

Descripción completa

Detalles Bibliográficos
Autores principales: Kaneya, Yohei, Takata, Hideyuki, Wada, Ryuichi, Kure, Shoko, Ishino, Kousuke, Kudo, Mitsuhiro, Kondo, Ryota, Taniai, Nobuhiko, Ohashi, Ryuji, Yoshida, Hiroshi, Naito, Zenya
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7681208/
https://www.ncbi.nlm.nih.gov/pubmed/33240434
http://dx.doi.org/10.3892/ol.2020.12289
_version_ 1783612592134029312
author Kaneya, Yohei
Takata, Hideyuki
Wada, Ryuichi
Kure, Shoko
Ishino, Kousuke
Kudo, Mitsuhiro
Kondo, Ryota
Taniai, Nobuhiko
Ohashi, Ryuji
Yoshida, Hiroshi
Naito, Zenya
author_facet Kaneya, Yohei
Takata, Hideyuki
Wada, Ryuichi
Kure, Shoko
Ishino, Kousuke
Kudo, Mitsuhiro
Kondo, Ryota
Taniai, Nobuhiko
Ohashi, Ryuji
Yoshida, Hiroshi
Naito, Zenya
author_sort Kaneya, Yohei
collection PubMed
description mTOR is involved in the proliferation of liver cancer. However, the clinical benefit of treatment with mTOR inhibitors for liver cancer is controversial. Protein disulfide isomerase A member 3 (PDIA3) is a chaperone protein, and it supports the assembly of mTOR complex 1 (mTORC1) and stabilizes signaling. Inhibition of PDIA3 function by a small molecule known as 16F16 may destabilize mTORC1 and enhance the effect of the mTOR inhibitor everolimus (Ev). The aim of the present study was to elucidate the usefulness of combination treatment with Ev and 16F16 in liver cancer using cultured Li-7 and HuH-6 cells. The proliferation of cultured cells was examined following treatment with 0.01 µM Ev, 2 µM 16F16 or both. The expression levels and phosphorylation of S6 kinase (S6K) and 4E-binding protein 1 (4E-BP1) were examined by western blotting. Li-7 was susceptible to Ev, and proliferation was reduced to 69.5±7.2% by Ev compared with that of untreated cells. Proliferation was reduced to 90.2±10.8% by 16F16 but to 62.3±12.2% by combination treatment with Ev and 16F16. HuH-6 cells were resistant to Ev, and proliferation was reduced to 86.7±6.1% by Ev and 86.6±4.8% by 16F16. However, combination treatment suppressed proliferation to 57.7±4.0%. Phosphorylation of S6K was reduced by Ev in both Li-7 and HuH-6 cells. Phosphorylation of 4E-BP1 was reduced by combination treatment in both Li-7 and HuH-6 cells. Immunoprecipitation assays demonstrated that PDIA3 formed a complex with 4E-BP1 but not with S6K. The small molecule 16F16 increased susceptibility to Ev in cultured liver cancer cells, which are resistant to Ev. The inhibition was associated with reduction of 4E-BP1 phosphorylation, which formed a complex with PDIA3. Combination treatment with Ev and 16F16 could be a novel therapeutic strategy for liver cancer.
format Online
Article
Text
id pubmed-7681208
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher D.A. Spandidos
record_format MEDLINE/PubMed
spelling pubmed-76812082020-11-24 Inhibitor for protein disulfide-isomerase family A member 3 enhances the antiproliferative effect of inhibitor for mechanistic target of rapamycin in liver cancer: An in vitro study on combination treatment with everolimus and 16F16 Kaneya, Yohei Takata, Hideyuki Wada, Ryuichi Kure, Shoko Ishino, Kousuke Kudo, Mitsuhiro Kondo, Ryota Taniai, Nobuhiko Ohashi, Ryuji Yoshida, Hiroshi Naito, Zenya Oncol Lett Articles mTOR is involved in the proliferation of liver cancer. However, the clinical benefit of treatment with mTOR inhibitors for liver cancer is controversial. Protein disulfide isomerase A member 3 (PDIA3) is a chaperone protein, and it supports the assembly of mTOR complex 1 (mTORC1) and stabilizes signaling. Inhibition of PDIA3 function by a small molecule known as 16F16 may destabilize mTORC1 and enhance the effect of the mTOR inhibitor everolimus (Ev). The aim of the present study was to elucidate the usefulness of combination treatment with Ev and 16F16 in liver cancer using cultured Li-7 and HuH-6 cells. The proliferation of cultured cells was examined following treatment with 0.01 µM Ev, 2 µM 16F16 or both. The expression levels and phosphorylation of S6 kinase (S6K) and 4E-binding protein 1 (4E-BP1) were examined by western blotting. Li-7 was susceptible to Ev, and proliferation was reduced to 69.5±7.2% by Ev compared with that of untreated cells. Proliferation was reduced to 90.2±10.8% by 16F16 but to 62.3±12.2% by combination treatment with Ev and 16F16. HuH-6 cells were resistant to Ev, and proliferation was reduced to 86.7±6.1% by Ev and 86.6±4.8% by 16F16. However, combination treatment suppressed proliferation to 57.7±4.0%. Phosphorylation of S6K was reduced by Ev in both Li-7 and HuH-6 cells. Phosphorylation of 4E-BP1 was reduced by combination treatment in both Li-7 and HuH-6 cells. Immunoprecipitation assays demonstrated that PDIA3 formed a complex with 4E-BP1 but not with S6K. The small molecule 16F16 increased susceptibility to Ev in cultured liver cancer cells, which are resistant to Ev. The inhibition was associated with reduction of 4E-BP1 phosphorylation, which formed a complex with PDIA3. Combination treatment with Ev and 16F16 could be a novel therapeutic strategy for liver cancer. D.A. Spandidos 2021-01 2020-11-11 /pmc/articles/PMC7681208/ /pubmed/33240434 http://dx.doi.org/10.3892/ol.2020.12289 Text en Copyright: © Kaneya et al. This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , 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 Articles
Kaneya, Yohei
Takata, Hideyuki
Wada, Ryuichi
Kure, Shoko
Ishino, Kousuke
Kudo, Mitsuhiro
Kondo, Ryota
Taniai, Nobuhiko
Ohashi, Ryuji
Yoshida, Hiroshi
Naito, Zenya
Inhibitor for protein disulfide-isomerase family A member 3 enhances the antiproliferative effect of inhibitor for mechanistic target of rapamycin in liver cancer: An in vitro study on combination treatment with everolimus and 16F16
title Inhibitor for protein disulfide-isomerase family A member 3 enhances the antiproliferative effect of inhibitor for mechanistic target of rapamycin in liver cancer: An in vitro study on combination treatment with everolimus and 16F16
title_full Inhibitor for protein disulfide-isomerase family A member 3 enhances the antiproliferative effect of inhibitor for mechanistic target of rapamycin in liver cancer: An in vitro study on combination treatment with everolimus and 16F16
title_fullStr Inhibitor for protein disulfide-isomerase family A member 3 enhances the antiproliferative effect of inhibitor for mechanistic target of rapamycin in liver cancer: An in vitro study on combination treatment with everolimus and 16F16
title_full_unstemmed Inhibitor for protein disulfide-isomerase family A member 3 enhances the antiproliferative effect of inhibitor for mechanistic target of rapamycin in liver cancer: An in vitro study on combination treatment with everolimus and 16F16
title_short Inhibitor for protein disulfide-isomerase family A member 3 enhances the antiproliferative effect of inhibitor for mechanistic target of rapamycin in liver cancer: An in vitro study on combination treatment with everolimus and 16F16
title_sort inhibitor for protein disulfide-isomerase family a member 3 enhances the antiproliferative effect of inhibitor for mechanistic target of rapamycin in liver cancer: an in vitro study on combination treatment with everolimus and 16f16
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7681208/
https://www.ncbi.nlm.nih.gov/pubmed/33240434
http://dx.doi.org/10.3892/ol.2020.12289
work_keys_str_mv AT kaneyayohei inhibitorforproteindisulfideisomerasefamilyamember3enhancestheantiproliferativeeffectofinhibitorformechanistictargetofrapamycininlivercanceraninvitrostudyoncombinationtreatmentwitheverolimusand16f16
AT takatahideyuki inhibitorforproteindisulfideisomerasefamilyamember3enhancestheantiproliferativeeffectofinhibitorformechanistictargetofrapamycininlivercanceraninvitrostudyoncombinationtreatmentwitheverolimusand16f16
AT wadaryuichi inhibitorforproteindisulfideisomerasefamilyamember3enhancestheantiproliferativeeffectofinhibitorformechanistictargetofrapamycininlivercanceraninvitrostudyoncombinationtreatmentwitheverolimusand16f16
AT kureshoko inhibitorforproteindisulfideisomerasefamilyamember3enhancestheantiproliferativeeffectofinhibitorformechanistictargetofrapamycininlivercanceraninvitrostudyoncombinationtreatmentwitheverolimusand16f16
AT ishinokousuke inhibitorforproteindisulfideisomerasefamilyamember3enhancestheantiproliferativeeffectofinhibitorformechanistictargetofrapamycininlivercanceraninvitrostudyoncombinationtreatmentwitheverolimusand16f16
AT kudomitsuhiro inhibitorforproteindisulfideisomerasefamilyamember3enhancestheantiproliferativeeffectofinhibitorformechanistictargetofrapamycininlivercanceraninvitrostudyoncombinationtreatmentwitheverolimusand16f16
AT kondoryota inhibitorforproteindisulfideisomerasefamilyamember3enhancestheantiproliferativeeffectofinhibitorformechanistictargetofrapamycininlivercanceraninvitrostudyoncombinationtreatmentwitheverolimusand16f16
AT taniainobuhiko inhibitorforproteindisulfideisomerasefamilyamember3enhancestheantiproliferativeeffectofinhibitorformechanistictargetofrapamycininlivercanceraninvitrostudyoncombinationtreatmentwitheverolimusand16f16
AT ohashiryuji inhibitorforproteindisulfideisomerasefamilyamember3enhancestheantiproliferativeeffectofinhibitorformechanistictargetofrapamycininlivercanceraninvitrostudyoncombinationtreatmentwitheverolimusand16f16
AT yoshidahiroshi inhibitorforproteindisulfideisomerasefamilyamember3enhancestheantiproliferativeeffectofinhibitorformechanistictargetofrapamycininlivercanceraninvitrostudyoncombinationtreatmentwitheverolimusand16f16
AT naitozenya inhibitorforproteindisulfideisomerasefamilyamember3enhancestheantiproliferativeeffectofinhibitorformechanistictargetofrapamycininlivercanceraninvitrostudyoncombinationtreatmentwitheverolimusand16f16