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Visinin‐like 1, a novel target gene of the Wnt/β‐catenin signaling pathway, is involved in apoptosis resistance in colorectal cancer

BACKGROUND: Abnormal activation of Wnt/β‐catenin signaling is associated with various aspects of cancer development. This study explored the roles of novel target genes of the Wnt/β‐catenin signaling pathway in cancer cells. METHODS: Using the haploid chronic myelogenous leukemia cell line HAP1, RNA...

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Autores principales: Tage, Hiroki, Yamaguchi, Kiyoshi, Nakagawa, Saya, Kasuga, So, Takane, Kiyoko, Furukawa, Yoichi, Ikenoue, Tsuneo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10315817/
https://www.ncbi.nlm.nih.gov/pubmed/37096864
http://dx.doi.org/10.1002/cam4.5970
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author Tage, Hiroki
Yamaguchi, Kiyoshi
Nakagawa, Saya
Kasuga, So
Takane, Kiyoko
Furukawa, Yoichi
Ikenoue, Tsuneo
author_facet Tage, Hiroki
Yamaguchi, Kiyoshi
Nakagawa, Saya
Kasuga, So
Takane, Kiyoko
Furukawa, Yoichi
Ikenoue, Tsuneo
author_sort Tage, Hiroki
collection PubMed
description BACKGROUND: Abnormal activation of Wnt/β‐catenin signaling is associated with various aspects of cancer development. This study explored the roles of novel target genes of the Wnt/β‐catenin signaling pathway in cancer cells. METHODS: Using the haploid chronic myelogenous leukemia cell line HAP1, RNA sequencing (RNA‐seq) was performed to identify genes whose expression was increased by APC disruption and reversed by β‐catenin knockdown (KD). The regulatory mechanism and function of one of the candidate genes was investigated in colorectal cancer (CRC) cells. RESULTS: In total, 64 candidate genes whose expression was regulated by Wnt/β‐catenin signaling were identified. Of these candidate genes, the expression levels of six were reduced by β‐catenin KD in HCT116 CRC cells in our previous microarray. One of these genes was Visinin‐like 1 (VSNL1), which belongs to the neuronal calcium‐sensor gene family. The expression of VSNL1 was regulated by the β‐catenin/TCF7L2 complex via two TCF7L2‐binding elements in intron 1. VSNL1 KD‐induced apoptosis in VSNL1‐positive CRC cells. Additionally, forced expression of wild‐type VSNL1, but not a myristoylation, Ca(2+)‐binding, or dimerization‐defective mutant, suppressed the apoptosis induced by camptothecin and doxorubicin in VSNL1‐negative CRC cells. CONCLUSION: Our findings suggest that VSNL1, a novel target gene of the Wnt/β‐catenin signaling pathway, is associated with apoptosis resistance in CRC cells.
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spelling pubmed-103158172023-07-04 Visinin‐like 1, a novel target gene of the Wnt/β‐catenin signaling pathway, is involved in apoptosis resistance in colorectal cancer Tage, Hiroki Yamaguchi, Kiyoshi Nakagawa, Saya Kasuga, So Takane, Kiyoko Furukawa, Yoichi Ikenoue, Tsuneo Cancer Med RESEARCH ARTICLES BACKGROUND: Abnormal activation of Wnt/β‐catenin signaling is associated with various aspects of cancer development. This study explored the roles of novel target genes of the Wnt/β‐catenin signaling pathway in cancer cells. METHODS: Using the haploid chronic myelogenous leukemia cell line HAP1, RNA sequencing (RNA‐seq) was performed to identify genes whose expression was increased by APC disruption and reversed by β‐catenin knockdown (KD). The regulatory mechanism and function of one of the candidate genes was investigated in colorectal cancer (CRC) cells. RESULTS: In total, 64 candidate genes whose expression was regulated by Wnt/β‐catenin signaling were identified. Of these candidate genes, the expression levels of six were reduced by β‐catenin KD in HCT116 CRC cells in our previous microarray. One of these genes was Visinin‐like 1 (VSNL1), which belongs to the neuronal calcium‐sensor gene family. The expression of VSNL1 was regulated by the β‐catenin/TCF7L2 complex via two TCF7L2‐binding elements in intron 1. VSNL1 KD‐induced apoptosis in VSNL1‐positive CRC cells. Additionally, forced expression of wild‐type VSNL1, but not a myristoylation, Ca(2+)‐binding, or dimerization‐defective mutant, suppressed the apoptosis induced by camptothecin and doxorubicin in VSNL1‐negative CRC cells. CONCLUSION: Our findings suggest that VSNL1, a novel target gene of the Wnt/β‐catenin signaling pathway, is associated with apoptosis resistance in CRC cells. John Wiley and Sons Inc. 2023-04-25 /pmc/articles/PMC10315817/ /pubmed/37096864 http://dx.doi.org/10.1002/cam4.5970 Text en © 2023 The Authors. Cancer Medicine published by John Wiley & Sons Ltd. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle RESEARCH ARTICLES
Tage, Hiroki
Yamaguchi, Kiyoshi
Nakagawa, Saya
Kasuga, So
Takane, Kiyoko
Furukawa, Yoichi
Ikenoue, Tsuneo
Visinin‐like 1, a novel target gene of the Wnt/β‐catenin signaling pathway, is involved in apoptosis resistance in colorectal cancer
title Visinin‐like 1, a novel target gene of the Wnt/β‐catenin signaling pathway, is involved in apoptosis resistance in colorectal cancer
title_full Visinin‐like 1, a novel target gene of the Wnt/β‐catenin signaling pathway, is involved in apoptosis resistance in colorectal cancer
title_fullStr Visinin‐like 1, a novel target gene of the Wnt/β‐catenin signaling pathway, is involved in apoptosis resistance in colorectal cancer
title_full_unstemmed Visinin‐like 1, a novel target gene of the Wnt/β‐catenin signaling pathway, is involved in apoptosis resistance in colorectal cancer
title_short Visinin‐like 1, a novel target gene of the Wnt/β‐catenin signaling pathway, is involved in apoptosis resistance in colorectal cancer
title_sort visinin‐like 1, a novel target gene of the wnt/β‐catenin signaling pathway, is involved in apoptosis resistance in colorectal cancer
topic RESEARCH ARTICLES
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10315817/
https://www.ncbi.nlm.nih.gov/pubmed/37096864
http://dx.doi.org/10.1002/cam4.5970
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