Tumor volume of colon carcinoma is related to the invasive pattern but not to the expression of cell adhesion proteins
- PMID: 19245593
- DOI: 10.1111/j.1600-0463.2008.00011.x
Tumor volume of colon carcinoma is related to the invasive pattern but not to the expression of cell adhesion proteins
Abstract
Tumor volume increases during growth and due to tumor progression various mutations appear that may cause phenotypic changes. The invasive pattern may thus be affected resulting in a more disorganized growth. This phenomenon might be due to mutations in the genome of the adhesion proteins, which are responsible for the structural integrity of epithelial tissue. Tumor volume was assessed in whole mount sections of 33 colon carcinomas using Cavalieri's principle. Images from the entire invasive border were captured and used for calculating the irregularity of the border (Complexity Index). The expression of the adhesion proteins E-cadherin, beta-catenin, Claudin 2 and Occludin was assessed after immunohistochemical staining of two randomly selected areas of the invasive front of the tumor. Statistical significance for differences in volume was obtained for tumor Complexity Index, tumor stage (pT) and lymph node status (pN). Expression of adhesion proteins was significantly perturbed in the tumors compared with normal mucosa but only infrequently correlated to tumor differentiation or invasive pattern. The results show that when tumor volume increases the invasive pattern becomes more irregular which is compatible with tumor progression. A direct contribution of adhesion protein derangement to this process appears to be insignificant.
Similar articles
-
Disturbed expression of E-cadherin, beta-catenin and tight junction proteins in colon carcinoma is unrelated to growth pattern and genetic polymorphisms.APMIS. 2008 Apr;116(4):253-62. doi: 10.1111/j.1600-0463.2008.00894.x. APMIS. 2008. PMID: 18397460
-
Malignant progression of invasive tumour cells seen in hypoxia present an accumulation of beta-catenin in the nucleus at the tumour front.Exp Mol Pathol. 2009 Oct;87(2):109-16. doi: 10.1016/j.yexmp.2009.05.004. Epub 2009 May 28. Exp Mol Pathol. 2009. PMID: 19481539
-
Altered expression of epithelial junctional proteins in atopic asthma: possible role in inflammation.Can J Physiol Pharmacol. 2008 Mar;86(3):105-12. doi: 10.1139/y08-004. Can J Physiol Pharmacol. 2008. PMID: 18418437
-
Molecular aspects of the loss of cell adhesion and gain of invasiveness in carcinomas.Princess Takamatsu Symp. 1994;24:214-32. Princess Takamatsu Symp. 1994. PMID: 8983077 Review.
-
L1 cell adhesion molecule (L1CAM) in invasive tumors.Cancer Lett. 2009 Sep 18;282(2):137-45. doi: 10.1016/j.canlet.2008.12.021. Epub 2009 Jan 13. Cancer Lett. 2009. PMID: 19144458 Review.
Cited by
-
Macrophages induce "budding" in aggressive human colon cancer subtypes by protease-mediated disruption of tight junctions.Oncotarget. 2018 Apr 13;9(28):19490-19507. doi: 10.18632/oncotarget.24626. eCollection 2018 Apr 13. Oncotarget. 2018. PMID: 29731961 Free PMC article.
-
Effects of supplemental calcium and vitamin D on tight-junction proteins and mucin-12 expression in the normal rectal mucosa of colorectal adenoma patients.Mol Carcinog. 2019 Jul;58(7):1279-1290. doi: 10.1002/mc.23010. Epub 2019 Apr 2. Mol Carcinog. 2019. PMID: 30938860 Free PMC article. Clinical Trial.
-
Investigating the association between polymorphisms in connective tissue growth factor and susceptibility to colon carcinoma.Mol Med Rep. 2015 Apr;11(4):2493-503. doi: 10.3892/mmr.2014.3083. Epub 2014 Dec 11. Mol Med Rep. 2015. PMID: 25502877 Free PMC article.
-
Claudin Family Participates in the Pathogenesis of Inflammatory Bowel Diseases and Colitis-Associated Colorectal Cancer.Front Immunol. 2019 Jun 27;10:1441. doi: 10.3389/fimmu.2019.01441. eCollection 2019. Front Immunol. 2019. PMID: 31316506 Free PMC article. Review.
-
Reduced occludin expression is related to unfavorable tumor phenotype and poor prognosis in many different tumor types: A tissue microarray study on 16,870 tumors.PLoS One. 2025 Apr 2;20(4):e0321105. doi: 10.1371/journal.pone.0321105. eCollection 2025. PLoS One. 2025. PMID: 40173205 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Miscellaneous