Cargando…
High Expression of RARβ Is a Favorable Factor in Colorectal Cancer
RARβ plays a critical role in cancer progression and is associated with several types of human cancer. It remains unclear, however, whether it is linked to the clinicopathological parameters of colorectal cancer (CRC). We therefore determined the expression of RARβ protein in patients with primary C...
Autores principales: | , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi
2019
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6421793/ https://www.ncbi.nlm.nih.gov/pubmed/30944670 http://dx.doi.org/10.1155/2019/7138754 |
_version_ | 1783404299650334720 |
---|---|
author | Wang, Wei Liu, Shuang Jiang, Chunyi Wang, Yan Zhu, Huijun Wang, XuDong |
author_facet | Wang, Wei Liu, Shuang Jiang, Chunyi Wang, Yan Zhu, Huijun Wang, XuDong |
author_sort | Wang, Wei |
collection | PubMed |
description | RARβ plays a critical role in cancer progression and is associated with several types of human cancer. It remains unclear, however, whether it is linked to the clinicopathological parameters of colorectal cancer (CRC). We therefore determined the expression of RARβ protein in patients with primary CRC and examined its relationship with clinical outcomes. RARβ expression in 234 samples of CRC patients and matched benign noncancerous tumors was detected by immunohistochemistry. RARβ mRNA expression was confirmed using the TCGA and Oncomine databases. COX regression analysis and Kaplan–Meier survival analysis were performed to determine the relationship between RARβ expression and CRC prognosis. Our results show that high expression of RARβ correlated with better prognosis in CRC patients. RARβ expression in CRC specimens was clearly lower than in peritumoral specimens (30.8% vs 58.8%, p < 0.001) and significantly correlated with gender (χ(2) = 3.926, p = 0.048), tumor differentiation (χ(2) = 5.978, p = 0.014), and tumor stage (χ(2) = 6.642, p = 0.036). Multivariate analyses further revealed that low RARβ expression (p = 0.001), distant metastasis (p = 0.001), tissue differentiation (p = 0.006), and tumor stage (p = 0.002) were associated with overall survival in CRC patients. In addition, Kaplan–Meier analysis indicated that increased RARβ expression in cytoplasm (p = 0.001) and early tumor TNM stage (p = 0.030) was associated with a more favorable outcome in patients with CRC. In conclusion, RARβ expression was strongly correlated with several clinicopathological factors of CRC and may represent a favorable prognostic marker in patients with CRC. |
format | Online Article Text |
id | pubmed-6421793 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Hindawi |
record_format | MEDLINE/PubMed |
spelling | pubmed-64217932019-04-03 High Expression of RARβ Is a Favorable Factor in Colorectal Cancer Wang, Wei Liu, Shuang Jiang, Chunyi Wang, Yan Zhu, Huijun Wang, XuDong Dis Markers Research Article RARβ plays a critical role in cancer progression and is associated with several types of human cancer. It remains unclear, however, whether it is linked to the clinicopathological parameters of colorectal cancer (CRC). We therefore determined the expression of RARβ protein in patients with primary CRC and examined its relationship with clinical outcomes. RARβ expression in 234 samples of CRC patients and matched benign noncancerous tumors was detected by immunohistochemistry. RARβ mRNA expression was confirmed using the TCGA and Oncomine databases. COX regression analysis and Kaplan–Meier survival analysis were performed to determine the relationship between RARβ expression and CRC prognosis. Our results show that high expression of RARβ correlated with better prognosis in CRC patients. RARβ expression in CRC specimens was clearly lower than in peritumoral specimens (30.8% vs 58.8%, p < 0.001) and significantly correlated with gender (χ(2) = 3.926, p = 0.048), tumor differentiation (χ(2) = 5.978, p = 0.014), and tumor stage (χ(2) = 6.642, p = 0.036). Multivariate analyses further revealed that low RARβ expression (p = 0.001), distant metastasis (p = 0.001), tissue differentiation (p = 0.006), and tumor stage (p = 0.002) were associated with overall survival in CRC patients. In addition, Kaplan–Meier analysis indicated that increased RARβ expression in cytoplasm (p = 0.001) and early tumor TNM stage (p = 0.030) was associated with a more favorable outcome in patients with CRC. In conclusion, RARβ expression was strongly correlated with several clinicopathological factors of CRC and may represent a favorable prognostic marker in patients with CRC. Hindawi 2019-03-03 /pmc/articles/PMC6421793/ /pubmed/30944670 http://dx.doi.org/10.1155/2019/7138754 Text en Copyright © 2019 Wei Wang et al. http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Wang, Wei Liu, Shuang Jiang, Chunyi Wang, Yan Zhu, Huijun Wang, XuDong High Expression of RARβ Is a Favorable Factor in Colorectal Cancer |
title | High Expression of RARβ Is a Favorable Factor in Colorectal Cancer |
title_full | High Expression of RARβ Is a Favorable Factor in Colorectal Cancer |
title_fullStr | High Expression of RARβ Is a Favorable Factor in Colorectal Cancer |
title_full_unstemmed | High Expression of RARβ Is a Favorable Factor in Colorectal Cancer |
title_short | High Expression of RARβ Is a Favorable Factor in Colorectal Cancer |
title_sort | high expression of rarβ is a favorable factor in colorectal cancer |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6421793/ https://www.ncbi.nlm.nih.gov/pubmed/30944670 http://dx.doi.org/10.1155/2019/7138754 |
work_keys_str_mv | AT wangwei highexpressionofrarbisafavorablefactorincolorectalcancer AT liushuang highexpressionofrarbisafavorablefactorincolorectalcancer AT jiangchunyi highexpressionofrarbisafavorablefactorincolorectalcancer AT wangyan highexpressionofrarbisafavorablefactorincolorectalcancer AT zhuhuijun highexpressionofrarbisafavorablefactorincolorectalcancer AT wangxudong highexpressionofrarbisafavorablefactorincolorectalcancer |