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High cytoplasmic YAP1 expression predicts a poor prognosis in patients with colorectal cancer

PURPOSE: Yes associated protein 1 (YAP1), which is a standout amongst the most essential effectors of the Hippo pathway, assumes a vital part in a few kinds of cancer. However, whether YAP1 is an oncogene in CRC (colorectal cancer) remains controversial, and the association between the subcellular l...

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Autores principales: Dong, Tianqi, Yuan, Yuncang, Xiang, Xudong, Sang, Shuping, Shen, Hao, Wang, Lei, Yang, Chunyan, Li, Fangfang, Li, Hongliang, Zheng, Shangyong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: PeerJ Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7680625/
https://www.ncbi.nlm.nih.gov/pubmed/33240680
http://dx.doi.org/10.7717/peerj.10397
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author Dong, Tianqi
Yuan, Yuncang
Xiang, Xudong
Sang, Shuping
Shen, Hao
Wang, Lei
Yang, Chunyan
Li, Fangfang
Li, Hongliang
Zheng, Shangyong
author_facet Dong, Tianqi
Yuan, Yuncang
Xiang, Xudong
Sang, Shuping
Shen, Hao
Wang, Lei
Yang, Chunyan
Li, Fangfang
Li, Hongliang
Zheng, Shangyong
author_sort Dong, Tianqi
collection PubMed
description PURPOSE: Yes associated protein 1 (YAP1), which is a standout amongst the most essential effectors of the Hippo pathway, assumes a vital part in a few kinds of cancer. However, whether YAP1 is an oncogene in CRC (colorectal cancer) remains controversial, and the association between the subcellular localization of YAP1 and clinical implications in CRC remains unknown. PATIENTS AND METHODS: In this study, we investigated the subcellular localization of YAP1 in CRC cells by immunohistochemistry and then associate these findings with clinical information in a large CRC cohort with 919 CRC patients. RESULTS: The results show that CRC tissues has a significant higher expression of cytoplasmic YAP1 compared to adjacent normal tissues (all P < 0.001). Cytoplasmic YAP1 expression was significantly associated with the number of lymph nodes removed and differentiation grade (all P < 0.001). Furthermore, after correcting confounding variables, for example, TNM stage and differentiation grade, the multivariate Cox analysis confirmed cytoplasmic YAP1-high subgroup had a significant shorter DFS (HR = 3.255; 95% CI [2.290–4.627]; P < 0.001) and DSS (HR = 4.049; 95% CI [2.400–6.830]; P < 0.001) than cytoplasmic YAP1-low subgroup. High cytoplasmic YAP1 expression is associated with a worse survival in stage III CRC patients who received chemotherapy. CONCLUSION: Cytoplasmic YAP1 could be could be utilized as a prognosis factor in CRC patients, and may be an indicator of whether certain patients population could benefit from postoperative chemotherapy.
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spelling pubmed-76806252020-11-24 High cytoplasmic YAP1 expression predicts a poor prognosis in patients with colorectal cancer Dong, Tianqi Yuan, Yuncang Xiang, Xudong Sang, Shuping Shen, Hao Wang, Lei Yang, Chunyan Li, Fangfang Li, Hongliang Zheng, Shangyong PeerJ Biochemistry PURPOSE: Yes associated protein 1 (YAP1), which is a standout amongst the most essential effectors of the Hippo pathway, assumes a vital part in a few kinds of cancer. However, whether YAP1 is an oncogene in CRC (colorectal cancer) remains controversial, and the association between the subcellular localization of YAP1 and clinical implications in CRC remains unknown. PATIENTS AND METHODS: In this study, we investigated the subcellular localization of YAP1 in CRC cells by immunohistochemistry and then associate these findings with clinical information in a large CRC cohort with 919 CRC patients. RESULTS: The results show that CRC tissues has a significant higher expression of cytoplasmic YAP1 compared to adjacent normal tissues (all P < 0.001). Cytoplasmic YAP1 expression was significantly associated with the number of lymph nodes removed and differentiation grade (all P < 0.001). Furthermore, after correcting confounding variables, for example, TNM stage and differentiation grade, the multivariate Cox analysis confirmed cytoplasmic YAP1-high subgroup had a significant shorter DFS (HR = 3.255; 95% CI [2.290–4.627]; P < 0.001) and DSS (HR = 4.049; 95% CI [2.400–6.830]; P < 0.001) than cytoplasmic YAP1-low subgroup. High cytoplasmic YAP1 expression is associated with a worse survival in stage III CRC patients who received chemotherapy. CONCLUSION: Cytoplasmic YAP1 could be could be utilized as a prognosis factor in CRC patients, and may be an indicator of whether certain patients population could benefit from postoperative chemotherapy. PeerJ Inc. 2020-11-19 /pmc/articles/PMC7680625/ /pubmed/33240680 http://dx.doi.org/10.7717/peerj.10397 Text en ©2020 Dong et al. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, reproduction and adaptation in any medium and for any purpose provided that it is properly attributed. For attribution, the original author(s), title, publication source (PeerJ) and either DOI or URL of the article must be cited.
spellingShingle Biochemistry
Dong, Tianqi
Yuan, Yuncang
Xiang, Xudong
Sang, Shuping
Shen, Hao
Wang, Lei
Yang, Chunyan
Li, Fangfang
Li, Hongliang
Zheng, Shangyong
High cytoplasmic YAP1 expression predicts a poor prognosis in patients with colorectal cancer
title High cytoplasmic YAP1 expression predicts a poor prognosis in patients with colorectal cancer
title_full High cytoplasmic YAP1 expression predicts a poor prognosis in patients with colorectal cancer
title_fullStr High cytoplasmic YAP1 expression predicts a poor prognosis in patients with colorectal cancer
title_full_unstemmed High cytoplasmic YAP1 expression predicts a poor prognosis in patients with colorectal cancer
title_short High cytoplasmic YAP1 expression predicts a poor prognosis in patients with colorectal cancer
title_sort high cytoplasmic yap1 expression predicts a poor prognosis in patients with colorectal cancer
topic Biochemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7680625/
https://www.ncbi.nlm.nih.gov/pubmed/33240680
http://dx.doi.org/10.7717/peerj.10397
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