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SPR965, a Dual PI3K/mTOR Inhibitor, as a Targeted Therapy in Ovarian Cancer

SPR965 is an inhibitor of PI3K and mTOR C1/C2 and has demonstrated anti-tumorigenic activity in a variety of solid tumors. We sought to determine the effects of SPR965 on cell proliferation and tumor growth in human serous ovarian cancer cell lines and a transgenic mouse model of high grade serous o...

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Autores principales: Tran, Arthur-Quan, Sullivan, Stephanie A., Chan, Leo Li-Ying, Yin, Yajie, Sun, Wenchuan, Fang, Ziwei, Dugar, Sundeep, Zhou, Chunxiao, Bae-Jump, Victoria
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7919852/
https://www.ncbi.nlm.nih.gov/pubmed/33659215
http://dx.doi.org/10.3389/fonc.2020.624498
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author Tran, Arthur-Quan
Sullivan, Stephanie A.
Chan, Leo Li-Ying
Yin, Yajie
Sun, Wenchuan
Fang, Ziwei
Dugar, Sundeep
Zhou, Chunxiao
Bae-Jump, Victoria
author_facet Tran, Arthur-Quan
Sullivan, Stephanie A.
Chan, Leo Li-Ying
Yin, Yajie
Sun, Wenchuan
Fang, Ziwei
Dugar, Sundeep
Zhou, Chunxiao
Bae-Jump, Victoria
author_sort Tran, Arthur-Quan
collection PubMed
description SPR965 is an inhibitor of PI3K and mTOR C1/C2 and has demonstrated anti-tumorigenic activity in a variety of solid tumors. We sought to determine the effects of SPR965 on cell proliferation and tumor growth in human serous ovarian cancer cell lines and a transgenic mouse model of high grade serous ovarian cancer (KpB model) and identify the underlying mechanisms by which SPR965 inhibits cell and tumor growth. SPR965 showed marked anti-proliferative activity by causing cell cycle arrest and inducing cellular stress in ovarian cancer cells. Treatment with SPR965 significantly inhibited tumor growth in KpB mice, accompanied by downregulation of Ki67 and VEGF and upregulation of Bip expression in ovarian tumors. SPR965 also inhibited adhesion and invasion through induction of the epithelial–mesenchymal transition process. As expected, downregulation of phosphorylation of AKT and S6 was observed in SPR965-treated ovarian cancer cells and tumors. Our results suggest that SPR965 has significant anti-tumorigenic effects in serous ovarian cancer in vitro and in vivo. Thus, SPR965 should be evaluated as a promising targeted agent in future clinical trials of ovarian cancer.
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spelling pubmed-79198522021-03-02 SPR965, a Dual PI3K/mTOR Inhibitor, as a Targeted Therapy in Ovarian Cancer Tran, Arthur-Quan Sullivan, Stephanie A. Chan, Leo Li-Ying Yin, Yajie Sun, Wenchuan Fang, Ziwei Dugar, Sundeep Zhou, Chunxiao Bae-Jump, Victoria Front Oncol Oncology SPR965 is an inhibitor of PI3K and mTOR C1/C2 and has demonstrated anti-tumorigenic activity in a variety of solid tumors. We sought to determine the effects of SPR965 on cell proliferation and tumor growth in human serous ovarian cancer cell lines and a transgenic mouse model of high grade serous ovarian cancer (KpB model) and identify the underlying mechanisms by which SPR965 inhibits cell and tumor growth. SPR965 showed marked anti-proliferative activity by causing cell cycle arrest and inducing cellular stress in ovarian cancer cells. Treatment with SPR965 significantly inhibited tumor growth in KpB mice, accompanied by downregulation of Ki67 and VEGF and upregulation of Bip expression in ovarian tumors. SPR965 also inhibited adhesion and invasion through induction of the epithelial–mesenchymal transition process. As expected, downregulation of phosphorylation of AKT and S6 was observed in SPR965-treated ovarian cancer cells and tumors. Our results suggest that SPR965 has significant anti-tumorigenic effects in serous ovarian cancer in vitro and in vivo. Thus, SPR965 should be evaluated as a promising targeted agent in future clinical trials of ovarian cancer. Frontiers Media S.A. 2021-02-15 /pmc/articles/PMC7919852/ /pubmed/33659215 http://dx.doi.org/10.3389/fonc.2020.624498 Text en Copyright © 2021 Tran, Sullivan, Chan, Yin, Sun, Fang, Dugar, Zhou and Bae-Jump http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Oncology
Tran, Arthur-Quan
Sullivan, Stephanie A.
Chan, Leo Li-Ying
Yin, Yajie
Sun, Wenchuan
Fang, Ziwei
Dugar, Sundeep
Zhou, Chunxiao
Bae-Jump, Victoria
SPR965, a Dual PI3K/mTOR Inhibitor, as a Targeted Therapy in Ovarian Cancer
title SPR965, a Dual PI3K/mTOR Inhibitor, as a Targeted Therapy in Ovarian Cancer
title_full SPR965, a Dual PI3K/mTOR Inhibitor, as a Targeted Therapy in Ovarian Cancer
title_fullStr SPR965, a Dual PI3K/mTOR Inhibitor, as a Targeted Therapy in Ovarian Cancer
title_full_unstemmed SPR965, a Dual PI3K/mTOR Inhibitor, as a Targeted Therapy in Ovarian Cancer
title_short SPR965, a Dual PI3K/mTOR Inhibitor, as a Targeted Therapy in Ovarian Cancer
title_sort spr965, a dual pi3k/mtor inhibitor, as a targeted therapy in ovarian cancer
topic Oncology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7919852/
https://www.ncbi.nlm.nih.gov/pubmed/33659215
http://dx.doi.org/10.3389/fonc.2020.624498
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