A novel chemical inhibitor suppresses breast cancer cell growth and metastasis through inhibiting HPIP oncoprotein

Abstract Increasing evidence suggests the pivotal role of hematopoietic pre-B-cell leukemia transcription factor (PBX)-interacting protein (HPIP/PBXIP1) in cancer development and progression, indicating that HPIP inhibition may be a promising target for cancer therapy. Here, we screened compounds in...

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Main Authors: Pengyun Li, Shengjie Cao, Yubing Huang, Yanan Zhang, Jie Liu, Xu Cai, Lulu Zhou, Jianbin Li, Zefei Jiang, Lihua Ding, Zhibing Zheng, Song Li, Qinong Ye
Format: Article
Language:English
Published: Nature Publishing Group 2021-07-01
Series:Cell Death Discovery
Online Access:https://doi.org/10.1038/s41420-021-00580-3
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spelling doaj-7915f9e9a46e40ef86dc654dbe8d6fce2021-08-01T11:11:55ZengNature Publishing GroupCell Death Discovery2058-77162021-07-017111210.1038/s41420-021-00580-3A novel chemical inhibitor suppresses breast cancer cell growth and metastasis through inhibiting HPIP oncoproteinPengyun Li0Shengjie Cao1Yubing Huang2Yanan Zhang3Jie Liu4Xu Cai5Lulu Zhou6Jianbin Li7Zefei Jiang8Lihua Ding9Zhibing Zheng10Song Li11Qinong Ye12Department of Medical Molecular Biology, Beijing Institute of BiotechnologyLaboratory of Computer-Aided Drug Design & Discovery, Beijing Institute of Pharmacology and ToxicologyDepartment of Medical Molecular Biology, Beijing Institute of BiotechnologyDepartment of Medical Molecular Biology, Beijing Institute of BiotechnologyDepartment of Medical Molecular Biology, Beijing Institute of BiotechnologyLaboratory of Computer-Aided Drug Design & Discovery, Beijing Institute of Pharmacology and ToxicologyLaboratory of Computer-Aided Drug Design & Discovery, Beijing Institute of Pharmacology and ToxicologyDepartment of Medical Molecular Biology, Beijing Institute of BiotechnologyFifth Medical Center of PLA General HospitalDepartment of Medical Molecular Biology, Beijing Institute of BiotechnologyLaboratory of Computer-Aided Drug Design & Discovery, Beijing Institute of Pharmacology and ToxicologyLaboratory of Computer-Aided Drug Design & Discovery, Beijing Institute of Pharmacology and ToxicologyDepartment of Medical Molecular Biology, Beijing Institute of BiotechnologyAbstract Increasing evidence suggests the pivotal role of hematopoietic pre-B-cell leukemia transcription factor (PBX)-interacting protein (HPIP/PBXIP1) in cancer development and progression, indicating that HPIP inhibition may be a promising target for cancer therapy. Here, we screened compounds inhibiting breast cancer cell proliferation with HPIP fused with green fluorescent protein as a reporter. A novel agent named TXX-1-10 derived from rimonabant, an antagonist of cannabinoid receptor 1 with anticancer effects, has been discovered to reduce HPIP expression and has greater inhibitory effects on breast cancer cell growth and metastasis in vitro and in vivo than rimonabant. TXX-1-10 regulates HPIP downstream targets, including several important kinases involved in cancer development and progression (e.g., AKT, ERK1/2, and FAK) as well as cell cycle-, apoptosis-, migration-, and epithelial-to-mesenchymal transition (EMT)-related genes. Consistent with the results of anticancer effects, genome-wide RNA sequencing indicated that TXX-1-10 has more significant effects on regulation of the expression of genes related to DNA replication, cell cycle, apoptosis, cell adhesion, cell migration, and invasion than rimonabant. In addition, TXX-1-10 significantly regulated genes associated with the cell growth and extracellular matrix organization, many of which were shown to be regulated by HPIP. Moreover, compared with rimonabant, TXX-1-10 greatly reduces blood-brain barrier penetrability to avoid adverse central depressive effects. These findings suggest that HPIP inhibition may be a useful strategy for cancer treatment and TXX-1-10 is a promising candidate drug for cancer therapy.https://doi.org/10.1038/s41420-021-00580-3
collection DOAJ
language English
format Article
sources DOAJ
author Pengyun Li
Shengjie Cao
Yubing Huang
Yanan Zhang
Jie Liu
Xu Cai
Lulu Zhou
Jianbin Li
Zefei Jiang
Lihua Ding
Zhibing Zheng
Song Li
Qinong Ye
spellingShingle Pengyun Li
Shengjie Cao
Yubing Huang
Yanan Zhang
Jie Liu
Xu Cai
Lulu Zhou
Jianbin Li
Zefei Jiang
Lihua Ding
Zhibing Zheng
Song Li
Qinong Ye
A novel chemical inhibitor suppresses breast cancer cell growth and metastasis through inhibiting HPIP oncoprotein
Cell Death Discovery
author_facet Pengyun Li
Shengjie Cao
Yubing Huang
Yanan Zhang
Jie Liu
Xu Cai
Lulu Zhou
Jianbin Li
Zefei Jiang
Lihua Ding
Zhibing Zheng
Song Li
Qinong Ye
author_sort Pengyun Li
title A novel chemical inhibitor suppresses breast cancer cell growth and metastasis through inhibiting HPIP oncoprotein
title_short A novel chemical inhibitor suppresses breast cancer cell growth and metastasis through inhibiting HPIP oncoprotein
title_full A novel chemical inhibitor suppresses breast cancer cell growth and metastasis through inhibiting HPIP oncoprotein
title_fullStr A novel chemical inhibitor suppresses breast cancer cell growth and metastasis through inhibiting HPIP oncoprotein
title_full_unstemmed A novel chemical inhibitor suppresses breast cancer cell growth and metastasis through inhibiting HPIP oncoprotein
title_sort novel chemical inhibitor suppresses breast cancer cell growth and metastasis through inhibiting hpip oncoprotein
publisher Nature Publishing Group
series Cell Death Discovery
issn 2058-7716
publishDate 2021-07-01
description Abstract Increasing evidence suggests the pivotal role of hematopoietic pre-B-cell leukemia transcription factor (PBX)-interacting protein (HPIP/PBXIP1) in cancer development and progression, indicating that HPIP inhibition may be a promising target for cancer therapy. Here, we screened compounds inhibiting breast cancer cell proliferation with HPIP fused with green fluorescent protein as a reporter. A novel agent named TXX-1-10 derived from rimonabant, an antagonist of cannabinoid receptor 1 with anticancer effects, has been discovered to reduce HPIP expression and has greater inhibitory effects on breast cancer cell growth and metastasis in vitro and in vivo than rimonabant. TXX-1-10 regulates HPIP downstream targets, including several important kinases involved in cancer development and progression (e.g., AKT, ERK1/2, and FAK) as well as cell cycle-, apoptosis-, migration-, and epithelial-to-mesenchymal transition (EMT)-related genes. Consistent with the results of anticancer effects, genome-wide RNA sequencing indicated that TXX-1-10 has more significant effects on regulation of the expression of genes related to DNA replication, cell cycle, apoptosis, cell adhesion, cell migration, and invasion than rimonabant. In addition, TXX-1-10 significantly regulated genes associated with the cell growth and extracellular matrix organization, many of which were shown to be regulated by HPIP. Moreover, compared with rimonabant, TXX-1-10 greatly reduces blood-brain barrier penetrability to avoid adverse central depressive effects. These findings suggest that HPIP inhibition may be a useful strategy for cancer treatment and TXX-1-10 is a promising candidate drug for cancer therapy.
url https://doi.org/10.1038/s41420-021-00580-3
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