β‐asarone inhibits the migration, invasion, and EMT of bladder cancer through activating ER stress

Abstract Background β‐asarone (β‐as), a compound extracted from Acorus calamus, has been found to have anticancer effects on a variety of human cancers. However, the potential effect of β‐as on bladder cancer (BCa) remains unknown. Methods After exposure to β‐as, migration, invasion, and epithelial‐...

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Main Authors: Bo Liu, Weichao Dan, Yi Wei, Yan Zhang, Chi Wang, Yuzeshi Lei, Tao Hou, Yong Zhang, Ye Gao
Format: Article
Language:English
Published: Wiley 2023-06-01
Series:Cancer Medicine
Subjects:
Online Access:https://doi.org/10.1002/cam4.6059
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author Bo Liu
Weichao Dan
Yi Wei
Yan Zhang
Chi Wang
Yuzeshi Lei
Tao Hou
Yong Zhang
Ye Gao
author_facet Bo Liu
Weichao Dan
Yi Wei
Yan Zhang
Chi Wang
Yuzeshi Lei
Tao Hou
Yong Zhang
Ye Gao
author_sort Bo Liu
collection DOAJ
description Abstract Background β‐asarone (β‐as), a compound extracted from Acorus calamus, has been found to have anticancer effects on a variety of human cancers. However, the potential effect of β‐as on bladder cancer (BCa) remains unknown. Methods After exposure to β‐as, migration, invasion, and epithelial‐mesenchymal transition (EMT) of BCa were determined by wound healing, transwell, and Western blot assays. Expression of proteins involved in the EMT and ER stress were explored by Western blot assays. Nude mouse xenograft model was served as the model system in vivo. Results The migration, invasion, and EMT of BCa were significantly inhibited after β‐as treatment. Further experiments revealed that endoplasmic reticulum (ER) stress is involved in β‐as‐mediated metastasis inhibition. In addition, β‐as significantly up‐regulated activating transcription factor 6 (ATF6), a branch of ER stress, and promoted its Golgi cleavage and nuclear localization. ATF6 silencing attenuated β‐as‐mediated metastasis and EMT inhibition in BCa cells. Conclusion Our data suggests that β‐as inhibits migration, invasion, and EMT of BCa by activating the ATF6 branch of ER stress. Thus, β‐as represents a potential candidate for BCa treatment.
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spelling doaj.art-63bd67a6081a447b84c21d7783d58c3e2023-07-21T11:20:58ZengWileyCancer Medicine2045-76342023-06-011212136101362210.1002/cam4.6059β‐asarone inhibits the migration, invasion, and EMT of bladder cancer through activating ER stressBo Liu0Weichao Dan1Yi Wei2Yan Zhang3Chi Wang4Yuzeshi Lei5Tao Hou6Yong Zhang7Ye Gao8Department of Surgical Oncology The First Affiliated Hospital of Xi'an Jiaotong University Xi'an P. R. ChinaDepartment of Urology The First Affiliated Hospital of Xi'an Jiaotong University Xi'an P. R. ChinaDepartment of Urology The First Affiliated Hospital of Xi'an Jiaotong University Xi'an P. R. ChinaDepartment of Surgical Oncology The First Affiliated Hospital of Xi'an Jiaotong University Xi'an P. R. ChinaDepartment of Urology The First Affiliated Hospital of Xi'an Jiaotong University Xi'an P. R. ChinaDepartment of Urology The First Affiliated Hospital of Xi'an Jiaotong University Xi'an P. R. ChinaDepartment of Urology The First Affiliated Hospital of Xi'an Jiaotong University Xi'an P. R. ChinaDepartment of Surgical Oncology The First Affiliated Hospital of Xi'an Jiaotong University Xi'an P. R. ChinaDepartment of Emergency The First Affiliated Hospital of Xi'an Jiaotong University Xi'an P. R. ChinaAbstract Background β‐asarone (β‐as), a compound extracted from Acorus calamus, has been found to have anticancer effects on a variety of human cancers. However, the potential effect of β‐as on bladder cancer (BCa) remains unknown. Methods After exposure to β‐as, migration, invasion, and epithelial‐mesenchymal transition (EMT) of BCa were determined by wound healing, transwell, and Western blot assays. Expression of proteins involved in the EMT and ER stress were explored by Western blot assays. Nude mouse xenograft model was served as the model system in vivo. Results The migration, invasion, and EMT of BCa were significantly inhibited after β‐as treatment. Further experiments revealed that endoplasmic reticulum (ER) stress is involved in β‐as‐mediated metastasis inhibition. In addition, β‐as significantly up‐regulated activating transcription factor 6 (ATF6), a branch of ER stress, and promoted its Golgi cleavage and nuclear localization. ATF6 silencing attenuated β‐as‐mediated metastasis and EMT inhibition in BCa cells. Conclusion Our data suggests that β‐as inhibits migration, invasion, and EMT of BCa by activating the ATF6 branch of ER stress. Thus, β‐as represents a potential candidate for BCa treatment.https://doi.org/10.1002/cam4.6059ATF6EMTER stressinvasionmigrationβ‐asarone
spellingShingle Bo Liu
Weichao Dan
Yi Wei
Yan Zhang
Chi Wang
Yuzeshi Lei
Tao Hou
Yong Zhang
Ye Gao
β‐asarone inhibits the migration, invasion, and EMT of bladder cancer through activating ER stress
Cancer Medicine
ATF6
EMT
ER stress
invasion
migration
β‐asarone
title β‐asarone inhibits the migration, invasion, and EMT of bladder cancer through activating ER stress
title_full β‐asarone inhibits the migration, invasion, and EMT of bladder cancer through activating ER stress
title_fullStr β‐asarone inhibits the migration, invasion, and EMT of bladder cancer through activating ER stress
title_full_unstemmed β‐asarone inhibits the migration, invasion, and EMT of bladder cancer through activating ER stress
title_short β‐asarone inhibits the migration, invasion, and EMT of bladder cancer through activating ER stress
title_sort β asarone inhibits the migration invasion and emt of bladder cancer through activating er stress
topic ATF6
EMT
ER stress
invasion
migration
β‐asarone
url https://doi.org/10.1002/cam4.6059
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