Transmembrane protein TMEM119 facilitates the stemness of breast cancer cells by activating Wnt/β-catenin pathway

The effects of transmembrane protein 119 (TMEM119) on breast cancer progression have not been elucidated. This study aims to investigate the roles of TMEM119 in breast cancer progression. Clinical samples and online datasets were used to determine TMEM119 expression and its correlation between patie...

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Main Authors: Ben Yang, Fengling Wang, Gang Zheng
Format: Article
Language:English
Published: Taylor & Francis Group 2021-01-01
Series:Bioengineered
Subjects:
Online Access:http://dx.doi.org/10.1080/21655979.2021.1960464
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spelling doaj-83225cf228c74fbbab1e3e9aa3a7e3632021-08-09T18:41:15ZengTaylor & Francis GroupBioengineered2165-59792165-59872021-01-011214856486710.1080/21655979.2021.19604641960464Transmembrane protein TMEM119 facilitates the stemness of breast cancer cells by activating Wnt/β-catenin pathwayBen Yang0Fengling Wang1Gang Zheng2Shandong Cancer Hospital, the Cancer Hospital Affiliated to Shandong First Medical UniversityShandong Cancer Hospital, the Cancer Hospital Affiliated to Shandong First Medical UniversityShandong Cancer Hospital, the Cancer Hospital Affiliated to Shandong First Medical UniversityThe effects of transmembrane protein 119 (TMEM119) on breast cancer progression have not been elucidated. This study aims to investigate the roles of TMEM119 in breast cancer progression. Clinical samples and online datasets were used to determine TMEM119 expression and its correlation between patients’ survival. Wound healing, transwell invasion, mammary spheroid formation, and ALDH activity were performed to detect the effects of TMEM119. RNA-sequencing, Luciferase report analysis, Co-IP, and ChIP analysis were constructed to reveal the underlying mechanisms. We found that TMEM119 was highly expressed in breast cancer tissues and cells compared to that in normal tissues and cells. Additionally, TMEM119 expression was negatively correlated with the survival of breast cancer patients. TMEM119 knockdown reduced the expression of stemness markers, mammary spheroid-formation ability and ALDH activity. RNA-sequencing analysis indicated that Wnt/β-catenin signaling was enriched in cells with TMEM119 overexpression. Further co-IP experiments indicated that TMEM119 interacted with β-catenin and maintained its protein stability. Conversely, β-catenin directly bound to TMEM119 gene promoter and thus increased TMEM119 transcriptional activity and its expression. Finally, we demonstrated that TMEM119-mediated effects depended on Wnt/β-catenin signaling. Thus, this work reveals a novel TMEM119-β-catenin positive feedback loop essential for breast cancer cell stemness.http://dx.doi.org/10.1080/21655979.2021.1960464tmem119breast cancerstemnesswnt/β-cateninfeedback loop
collection DOAJ
language English
format Article
sources DOAJ
author Ben Yang
Fengling Wang
Gang Zheng
spellingShingle Ben Yang
Fengling Wang
Gang Zheng
Transmembrane protein TMEM119 facilitates the stemness of breast cancer cells by activating Wnt/β-catenin pathway
Bioengineered
tmem119
breast cancer
stemness
wnt/β-catenin
feedback loop
author_facet Ben Yang
Fengling Wang
Gang Zheng
author_sort Ben Yang
title Transmembrane protein TMEM119 facilitates the stemness of breast cancer cells by activating Wnt/β-catenin pathway
title_short Transmembrane protein TMEM119 facilitates the stemness of breast cancer cells by activating Wnt/β-catenin pathway
title_full Transmembrane protein TMEM119 facilitates the stemness of breast cancer cells by activating Wnt/β-catenin pathway
title_fullStr Transmembrane protein TMEM119 facilitates the stemness of breast cancer cells by activating Wnt/β-catenin pathway
title_full_unstemmed Transmembrane protein TMEM119 facilitates the stemness of breast cancer cells by activating Wnt/β-catenin pathway
title_sort transmembrane protein tmem119 facilitates the stemness of breast cancer cells by activating wnt/β-catenin pathway
publisher Taylor & Francis Group
series Bioengineered
issn 2165-5979
2165-5987
publishDate 2021-01-01
description The effects of transmembrane protein 119 (TMEM119) on breast cancer progression have not been elucidated. This study aims to investigate the roles of TMEM119 in breast cancer progression. Clinical samples and online datasets were used to determine TMEM119 expression and its correlation between patients’ survival. Wound healing, transwell invasion, mammary spheroid formation, and ALDH activity were performed to detect the effects of TMEM119. RNA-sequencing, Luciferase report analysis, Co-IP, and ChIP analysis were constructed to reveal the underlying mechanisms. We found that TMEM119 was highly expressed in breast cancer tissues and cells compared to that in normal tissues and cells. Additionally, TMEM119 expression was negatively correlated with the survival of breast cancer patients. TMEM119 knockdown reduced the expression of stemness markers, mammary spheroid-formation ability and ALDH activity. RNA-sequencing analysis indicated that Wnt/β-catenin signaling was enriched in cells with TMEM119 overexpression. Further co-IP experiments indicated that TMEM119 interacted with β-catenin and maintained its protein stability. Conversely, β-catenin directly bound to TMEM119 gene promoter and thus increased TMEM119 transcriptional activity and its expression. Finally, we demonstrated that TMEM119-mediated effects depended on Wnt/β-catenin signaling. Thus, this work reveals a novel TMEM119-β-catenin positive feedback loop essential for breast cancer cell stemness.
topic tmem119
breast cancer
stemness
wnt/β-catenin
feedback loop
url http://dx.doi.org/10.1080/21655979.2021.1960464
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AT fenglingwang transmembraneproteintmem119facilitatesthestemnessofbreastcancercellsbyactivatingwntbcateninpathway
AT gangzheng transmembraneproteintmem119facilitatesthestemnessofbreastcancercellsbyactivatingwntbcateninpathway
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