Cargando…

Recurrences in stage II rectal carcinoma after curative resection alone: from the viewpoint of angiogenesis

BACKGROUND: Angiogenesis plays a pivotal role in malignant tumor progression. The count of blood microvessels of the tumor has been recognized as an indicator of malignant potential of the tumors and provides the ability to predict tumors recurrence. The role endoglin in the Dukes B rectal cancer is...

Descripción completa

Detalles Bibliográficos
Autores principales: Martinović, Željko, Kovač, Dražen, Martinović, Cvita
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4840965/
https://www.ncbi.nlm.nih.gov/pubmed/27102733
http://dx.doi.org/10.1186/s12957-016-0877-6
_version_ 1782428327473053696
author Martinović, Željko
Kovač, Dražen
Martinović, Cvita
author_facet Martinović, Željko
Kovač, Dražen
Martinović, Cvita
author_sort Martinović, Željko
collection PubMed
description BACKGROUND: Angiogenesis plays a pivotal role in malignant tumor progression. The count of blood microvessels of the tumor has been recognized as an indicator of malignant potential of the tumors and provides the ability to predict tumors recurrence. The role endoglin in the Dukes B rectal cancer is still unexplored. The aims of this study were to examine immunohistochemical expression of endoglin in resected rectal cancer and investigate the relationship of tumor recurrence and other clinicopathological variables to the endoglin-assessed microvessel density of the tumor tissue and distal resection margins. METHODS: The study included 95 primary rectal adenocarcinomas, corresponding to 95 distal and 95 proximal resection margin specimens from surgical resection samples. Tumor specimens were paraffin embedded, and immunohistochemical staining for the CD105 endothelial antigen was performed to count CD105-MVD. For exact measurement of the CD105-MVD used, a computer-integrated system Alphelys Spot Browser 2 was used. RESULTS: The MVD was significantly higher in the tumor samples compared with the distal resection margins (p < 0.0001) and the proximal resection margins (p < 0.0001). There was no significant difference in the MVD between distal and proximal resection margins (p = 0.147). The type of surgical resection was a significant factor for determining the recurrence of tumors (p = 0.0104). There was no significant effect of patients’ age, gender, tumor location, grade of differentiation, histological tumor type, and the size and depth of tumor invasion on the recurrence of the tumor. The recurrence rate was significantly higher in the low CD105-MVD group of patients than in the high CD105-MVD group of patients (log rank test, p = 0.0406). Result of the multivariate analysis showed that the type of surgery (p = 0.0086), MVD tumors (p = 0.0385), and MVD of proximal resection margin (p = 0.0218) were the independent prognostic factors for the recurrent tumors. CONCLUSIONS: CD105-assessed MVD could help to identify patients with more aggressive disease and increased risk of developing tumor recurrence after surgical treatment in stage II rectal cancer (RC).
format Online
Article
Text
id pubmed-4840965
institution National Center for Biotechnology Information
language English
publishDate 2016
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-48409652016-04-23 Recurrences in stage II rectal carcinoma after curative resection alone: from the viewpoint of angiogenesis Martinović, Željko Kovač, Dražen Martinović, Cvita World J Surg Oncol Research BACKGROUND: Angiogenesis plays a pivotal role in malignant tumor progression. The count of blood microvessels of the tumor has been recognized as an indicator of malignant potential of the tumors and provides the ability to predict tumors recurrence. The role endoglin in the Dukes B rectal cancer is still unexplored. The aims of this study were to examine immunohistochemical expression of endoglin in resected rectal cancer and investigate the relationship of tumor recurrence and other clinicopathological variables to the endoglin-assessed microvessel density of the tumor tissue and distal resection margins. METHODS: The study included 95 primary rectal adenocarcinomas, corresponding to 95 distal and 95 proximal resection margin specimens from surgical resection samples. Tumor specimens were paraffin embedded, and immunohistochemical staining for the CD105 endothelial antigen was performed to count CD105-MVD. For exact measurement of the CD105-MVD used, a computer-integrated system Alphelys Spot Browser 2 was used. RESULTS: The MVD was significantly higher in the tumor samples compared with the distal resection margins (p < 0.0001) and the proximal resection margins (p < 0.0001). There was no significant difference in the MVD between distal and proximal resection margins (p = 0.147). The type of surgical resection was a significant factor for determining the recurrence of tumors (p = 0.0104). There was no significant effect of patients’ age, gender, tumor location, grade of differentiation, histological tumor type, and the size and depth of tumor invasion on the recurrence of the tumor. The recurrence rate was significantly higher in the low CD105-MVD group of patients than in the high CD105-MVD group of patients (log rank test, p = 0.0406). Result of the multivariate analysis showed that the type of surgery (p = 0.0086), MVD tumors (p = 0.0385), and MVD of proximal resection margin (p = 0.0218) were the independent prognostic factors for the recurrent tumors. CONCLUSIONS: CD105-assessed MVD could help to identify patients with more aggressive disease and increased risk of developing tumor recurrence after surgical treatment in stage II rectal cancer (RC). BioMed Central 2016-04-22 /pmc/articles/PMC4840965/ /pubmed/27102733 http://dx.doi.org/10.1186/s12957-016-0877-6 Text en © Martinović et al. 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Martinović, Željko
Kovač, Dražen
Martinović, Cvita
Recurrences in stage II rectal carcinoma after curative resection alone: from the viewpoint of angiogenesis
title Recurrences in stage II rectal carcinoma after curative resection alone: from the viewpoint of angiogenesis
title_full Recurrences in stage II rectal carcinoma after curative resection alone: from the viewpoint of angiogenesis
title_fullStr Recurrences in stage II rectal carcinoma after curative resection alone: from the viewpoint of angiogenesis
title_full_unstemmed Recurrences in stage II rectal carcinoma after curative resection alone: from the viewpoint of angiogenesis
title_short Recurrences in stage II rectal carcinoma after curative resection alone: from the viewpoint of angiogenesis
title_sort recurrences in stage ii rectal carcinoma after curative resection alone: from the viewpoint of angiogenesis
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4840965/
https://www.ncbi.nlm.nih.gov/pubmed/27102733
http://dx.doi.org/10.1186/s12957-016-0877-6
work_keys_str_mv AT martinoviczeljko recurrencesinstageiirectalcarcinomaaftercurativeresectionalonefromtheviewpointofangiogenesis
AT kovacdrazen recurrencesinstageiirectalcarcinomaaftercurativeresectionalonefromtheviewpointofangiogenesis
AT martinoviccvita recurrencesinstageiirectalcarcinomaaftercurativeresectionalonefromtheviewpointofangiogenesis