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The predictive value of galectin-1 and vascular mimicry in the prognostic evaluation of patients with rectal cancer
BACKGROUND: This study aims to investigate the expression of galectin-1 and vascular mimicry (VM) in rectal cancer tissues, and to assess their predictive value in the prognostic evaluation of patients with rectal cancer. METHODS: Immunohistochemistry (IHC) and CD34-periodic acid solution (PAS) doub...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
AME Publishing Company
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8798531/ https://www.ncbi.nlm.nih.gov/pubmed/35116475 http://dx.doi.org/10.21037/tcr-21-121 |
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author | Zhou, Haihua Zhang, Degeng Yang, Minyan You, Xiaolan Zhang, Qi Fu, Xiaoyang Wang, Daorong |
author_facet | Zhou, Haihua Zhang, Degeng Yang, Minyan You, Xiaolan Zhang, Qi Fu, Xiaoyang Wang, Daorong |
author_sort | Zhou, Haihua |
collection | PubMed |
description | BACKGROUND: This study aims to investigate the expression of galectin-1 and vascular mimicry (VM) in rectal cancer tissues, and to assess their predictive value in the prognostic evaluation of patients with rectal cancer. METHODS: Immunohistochemistry (IHC) and CD34-periodic acid solution (PAS) double staining were used to detect galectin-1 expression and the formation of VM in rectal cancer tissues from 94 patients with stage I–III rectal cancer and their corresponding paracancerous tissues. We also analyzed the relationship between the expression of galectin-1, VM, various clinicopathological parameters, and the prognosis of rectal cancer patients, as well as their influence on the overall survival (OS) of rectal cancer patients. RESULTS: Among the 94 tissue specimens from rectal cancer patients, 43 had positive expression of galectin-1 and 19 had positive expression of VM. There was a positive correlation between VM and galectin-1 expression in rectal cancer tissue. Galectin-1 expression in rectal cancer tissue and the formation of VM were related to tumor differentiation, staging, lymph node metastasis, and intravascular tumor thrombus (P<0.05). Kaplan-Meier analysis showed that the OS time of rectal cancer patients in the galectin-1 positive expression group was shorter than the galectin-1 negative expression patients, and the difference between the 2 groups was statistically significant (P=0.003). The OS time of patients with rectal cancer in the VM positive expression group was shorter than the VM negative expression group, and the difference between the two groups was statistically significant (P<0.001). The OS time of the galectin-1 and VM negative expression group was 57.33±1.13 months, and the OS time of the galectin-1 and VM positive expression group was 43.21±3.97 months, while the OS time of the galectin-1 positive expression and VM negative expression group was 55.42±2.23 months, and the difference between the three groups was statistically significant (P<0.001). Multi-factor analysis results indicated that invasion depth and VM expression were independent risk factors that affected the OS of patients with rectal cancer. CONCLUSIONS: Galectin-1 and VM expression in rectal cancer tissues may predict poor prognosis in patients after radical surgery. Galectin-1 and VM may therefore become potential new targets for rectal cancer treatment. |
format | Online Article Text |
id | pubmed-8798531 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | AME Publishing Company |
record_format | MEDLINE/PubMed |
spelling | pubmed-87985312022-02-02 The predictive value of galectin-1 and vascular mimicry in the prognostic evaluation of patients with rectal cancer Zhou, Haihua Zhang, Degeng Yang, Minyan You, Xiaolan Zhang, Qi Fu, Xiaoyang Wang, Daorong Transl Cancer Res Original Article BACKGROUND: This study aims to investigate the expression of galectin-1 and vascular mimicry (VM) in rectal cancer tissues, and to assess their predictive value in the prognostic evaluation of patients with rectal cancer. METHODS: Immunohistochemistry (IHC) and CD34-periodic acid solution (PAS) double staining were used to detect galectin-1 expression and the formation of VM in rectal cancer tissues from 94 patients with stage I–III rectal cancer and their corresponding paracancerous tissues. We also analyzed the relationship between the expression of galectin-1, VM, various clinicopathological parameters, and the prognosis of rectal cancer patients, as well as their influence on the overall survival (OS) of rectal cancer patients. RESULTS: Among the 94 tissue specimens from rectal cancer patients, 43 had positive expression of galectin-1 and 19 had positive expression of VM. There was a positive correlation between VM and galectin-1 expression in rectal cancer tissue. Galectin-1 expression in rectal cancer tissue and the formation of VM were related to tumor differentiation, staging, lymph node metastasis, and intravascular tumor thrombus (P<0.05). Kaplan-Meier analysis showed that the OS time of rectal cancer patients in the galectin-1 positive expression group was shorter than the galectin-1 negative expression patients, and the difference between the 2 groups was statistically significant (P=0.003). The OS time of patients with rectal cancer in the VM positive expression group was shorter than the VM negative expression group, and the difference between the two groups was statistically significant (P<0.001). The OS time of the galectin-1 and VM negative expression group was 57.33±1.13 months, and the OS time of the galectin-1 and VM positive expression group was 43.21±3.97 months, while the OS time of the galectin-1 positive expression and VM negative expression group was 55.42±2.23 months, and the difference between the three groups was statistically significant (P<0.001). Multi-factor analysis results indicated that invasion depth and VM expression were independent risk factors that affected the OS of patients with rectal cancer. CONCLUSIONS: Galectin-1 and VM expression in rectal cancer tissues may predict poor prognosis in patients after radical surgery. Galectin-1 and VM may therefore become potential new targets for rectal cancer treatment. AME Publishing Company 2021-03 /pmc/articles/PMC8798531/ /pubmed/35116475 http://dx.doi.org/10.21037/tcr-21-121 Text en 2021 Translational Cancer Research. All rights reserved. https://creativecommons.org/licenses/by-nc-nd/4.0/Open Access Statement: This is an Open Access article distributed in accordance with the Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International License (CC BY-NC-ND 4.0), which permits the non-commercial replication and distribution of the article with the strict proviso that no changes or edits are made and the original work is properly cited (including links to both the formal publication through the relevant DOI and the license). See: https://creativecommons.org/licenses/by-nc-nd/4.0/. |
spellingShingle | Original Article Zhou, Haihua Zhang, Degeng Yang, Minyan You, Xiaolan Zhang, Qi Fu, Xiaoyang Wang, Daorong The predictive value of galectin-1 and vascular mimicry in the prognostic evaluation of patients with rectal cancer |
title | The predictive value of galectin-1 and vascular mimicry in the prognostic evaluation of patients with rectal cancer |
title_full | The predictive value of galectin-1 and vascular mimicry in the prognostic evaluation of patients with rectal cancer |
title_fullStr | The predictive value of galectin-1 and vascular mimicry in the prognostic evaluation of patients with rectal cancer |
title_full_unstemmed | The predictive value of galectin-1 and vascular mimicry in the prognostic evaluation of patients with rectal cancer |
title_short | The predictive value of galectin-1 and vascular mimicry in the prognostic evaluation of patients with rectal cancer |
title_sort | predictive value of galectin-1 and vascular mimicry in the prognostic evaluation of patients with rectal cancer |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8798531/ https://www.ncbi.nlm.nih.gov/pubmed/35116475 http://dx.doi.org/10.21037/tcr-21-121 |
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