Alantolactone inhibits proliferation, metastasis and promotes apoptosis of human osteosarcoma cells by suppressing Wnt/β-catenin and MAPKs signaling pathways
返回论文页
Full-length article|更新时间:2022-06-24
|
Alantolactone inhibits proliferation, metastasis and promotes apoptosis of human osteosarcoma cells by suppressing Wnt/β-catenin and MAPKs signaling pathways
Alantolactone inhibits proliferation, metastasis and promotes apoptosis of human osteosarcoma cells by suppressing Wnt/β-catenin and MAPKs signaling pathways
Genes & Diseases2022年9卷第2期
作者机构:
1. School of Laboratory Medicine, Chongqing Medical University,Chongqing,PR China,400016
2. Department of Orthopedics, The First Affiliated Hospital of Chongqing Medical University,Chongqing,PR China,400042
Chunmei Yang, Lulu Zhang, Huakun Huang, 等. Alantolactone inhibits proliferation, metastasis and promotes apoptosis of human osteosarcoma cells by suppressing Wnt/β-catenin and MAPKs signaling pathways[J]. Genes & Diseases, 2022,9(2).
Chunmei Yang, Lulu Zhang, Huakun Huang, et al. Alantolactone inhibits proliferation, metastasis and promotes apoptosis of human osteosarcoma cells by suppressing Wnt/β-catenin and MAPKs signaling pathways[J]. Genes & Diseases, 2022,9(2).
Chunmei Yang, Lulu Zhang, Huakun Huang, 等. Alantolactone inhibits proliferation, metastasis and promotes apoptosis of human osteosarcoma cells by suppressing Wnt/β-catenin and MAPKs signaling pathways[J]. Genes & Diseases, 2022,9(2). DOI: 10.1016/j.gendis.2020.07.014.
Chunmei Yang, Lulu Zhang, Huakun Huang, et al. Alantolactone inhibits proliferation, metastasis and promotes apoptosis of human osteosarcoma cells by suppressing Wnt/β-catenin and MAPKs signaling pathways[J]. Genes & Diseases, 2022,9(2). DOI: 10.1016/j.gendis.2020.07.014.
Alantolactone inhibits proliferation, metastasis and promotes apoptosis of human osteosarcoma cells by suppressing Wnt/β-catenin and MAPKs signaling pathways
摘要
Abstract
lthough there are many therapeutic strategies such as surgery and chemotherapy
the prognosis of osteosarcoma (OS) is still far from being satisfactory. It is urgent to develop more effective
tolerable and safe drugs for the treatment of OS. In the present study
we investigated the anti-OS activity of Alantolactone (ALT)
a natural eucalyptone sesquiterpene lactone mainly exists in Inula helenium
and probed the possible mechanism involved. We demonstrated that ALT significantly inhibited cell proliferation of various human OS cell lines while had relative lower cytotoxicity against normal cells. Then
we validated that ALT reduced migration
decreased invasion possibly through reversing epithelial mesenchymal transition (EMT) process and suppressing Matrix metalloproteinases (MMPs). Moreover
we confirmed that ALT promoted apoptosis and arrested cell cycle at G2/M phase of human OS cells
in vitro
. In addition
we confirmed that ALT restrained tumor growth and metastasis of OS 143 cells in a xenograft model
in vivo
. Mechanistically
ALT inhibited the activity of Wnt/β-catenin and p38
ERK1/2 and JNK Mitogen Activated Protein Kinases (MAPKs) signal pathway. Notably
the combination of ALT and Wnt/β-catenin inhibitor
as well as the combination of ALT and MAPKs inhibitors resulted in a synergistically effect on inhibiting the proliferation
migration and invasion of OS cells. Collectively
our results validate the ALT may inhibit proliferation
metastasis and promotes apoptosis of human OS cells possibly through suppressing Wnt/β-Catenin and MAPKs signaling pathways.
关键词
Keywords
AlantolactoneERK1/2JNKMitogen activated protein kinasesOsteosarcomap38Wnt/β-catenin
Echinatin inhibits tumor growth and synergizes with chemotherapeutic agents against human bladder cancer cells by activating p38 and suppressing Wnt/β-catenin pathways
The generation and use of animal models of osteosarcoma in cancer research
Integrative transcriptome analysis identifies MYBL2 as a poor prognosis marker for osteosarcoma and a pan-cancer marker of immune infiltration
Aberrant LETM1 elevation dysregulates mitochondrial functions and energy metabolism and promotes lung metastasis in osteosarcoma
Cellular senescence-driven transcriptional reprogramming of the MAFB/NOTCH3 axis activates the PI3K/AKT pathway and promotes osteosarcoma progression
相关作者
Xiaoxuan Wang
Lijuan Luo
Jingtao Xu
Qiuping Lu
Haichao Xia
Yanran Huang
Lulu Zhang
Liping Xie
相关机构
Key Laboratory of Diagnostic Medicine Designated By the Chinese Ministry of Education, School of Laboratory Medicine, Chongqing Medical University
Department of Orthopedics, The First Affiliated Hospital of Chongqing Medical University
Department of Orthopedics, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology
Department of Radiation and Medical Oncology, Zhongnan Hospital, Wuhan University
Department of Orthopedics, Wuhan Hospital of Traditional Chinese and Western Medicine (Wuhan No.1 Hospital), Tongji Medical College, Huazhong University of Science and Technology