Publication: Inter- and intra-tumoral relationships between vasculature characteristics, GLUT1 and budding in colorectal carcinoma
Authors
Mezheyeuski, Artur ; Nerovnya, Alexander ; Bich, Tatjana ; Tur, Gennadiy ; Ostman, Arne ; Portyanko, Anna
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Publisher
F. Hernández y Juan F. Madrid. Universidad de Murcia: Departamento de Biología Celular e Histología
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DOI
10.14670/HH-11-613
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info:eu-repo/semantics/article
Description
Abstract
Vascular characteristics, hypoxia and tumor
budding are features that have been implied in the
biology and prognosis of colorectal cancer. Internal
relationships and the inter- and intra-tumoral variation of
these tumor properties remain to be determined. In the
current study we have characterized blood vessel status
in different areas of CRC and in the peritumoral
fibroblastic stroma. Analyses of these characteristics
have been supplemented by characterization of budding
and hypoxia.
Analyses revealed significantly lower values of
vessel perimeter (VP) and vessel lumen area (VL) at the
invasive front and surrounding stroma as compared to
the tumor center. Also, the number of vessels (VN) in
the peritumoral stroma was higher than in the center.
Thus, tumor center displays larger and fewer vessels as
compared to the tumor periphery.
GLUT1 expression was correlated directly with VN
(r=0.351, p=0.028) and inversely with VL and VP (r=-
0.432, p=0.006 and r=-0.484, p=0.002) at the invasive
front. Moreover, GLUT1 expression, VP at the invasive
front, and VN in the surrounding peritumoral stroma,
were associated with budding score (r=0.574, p<0.000,
r=-0.340, p=0,034 and r=-0,389, p=0.025 respectively).
Furthermore, GLUT1, budding score, vessel number
in peritumoral stroma, and vessel size in the invasive
front, were significantly different in tumors with or
without lymph node metastasis.
This study reports previously unrecognized
relationships between localization-specific vascular
characteristics, hypoxia and tumor budding. The findings
suggest potential functional relationships, which should
be further explored, and also highlight the inter-tumoral
variations in vasculature, which is highly relevant for
ongoing efforts to identify vessel-based biomarkers.
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Citation
Histology and histopathology, Vol. 30, nº10, (2015)
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