Mesh structure of two-dimensional tumor microvascular architecture phenotype heterogeneity in non-small cell lung cancer.
- Author:
Zeng XIONG
1
;
Hui ZHOU
;
Jin-Kang LIU
;
Cheng-Ping HU
;
Mo-Ling ZHOU
;
Yu XIA
;
Jian-Hua ZHOU
Author Information
- Publication Type:Journal Article
- MeSH: Adult; Aged; Capillaries; ultrastructure; Carcinoma, Non-Small-Cell Lung; blood supply; diagnostic imaging; Female; Humans; Lung Neoplasms; blood supply; diagnostic imaging; Male; Middle Aged; Tomography, Spiral Computed
- From: Journal of Southern Medical University 2009;29(11):2215-2218
- CountryChina
- Language:Chinese
-
Abstract:
OBJECTIVETo investigate the structural characteristics and clinical significance of two-dimensional tumor microvascular architecture phenotype (2D-TMAP) in non-small cell lung cancer (NSCLC).
METHODSThirty surgical specimens of NSCLC were collected. The sections of the tumor tissues corresponding to the slice of CT perfusion imaging were selected to construct the 2D-TMAP expression. Spearman correlation analysis was used to examine the relation between the 2D-TMAP expression and the clinicopathological features of NSCLC.
RESULTSA heterogeneity was noted in the 2D-TMAP expression of NSCLC. The microvascular density (MVD) in the area surrounding the tumor was higher than that in the central area, but the difference was not statistically significant. The density of the microvessels without intact lumen was significantly greater in the surrounding area than in the central area (P=0.030). The total MVD was not correlated to tumor differentiation (r=0.042, P=0.831). The density of the microvessels without intact lumen in the surrounding area was positively correlated to degree of tumor differentiation and lymph node metastasis (r=0.528 and 0.533, P=0.041 and 0.028, respectively), and also to the expressions of vascular endothelial growth factor (VEGF), ephrinB2, EphB4, and proliferating cell nuclear antigen (PCNA) (r=0.504, 0.549, 0.549, and 0.370; P=0.005, 0.002, 0.002, and 0.048, respectively). The degree of tumor differentiation was positively correlated to PCNA and VEGF expression (r=0.604 and 0.370, P=0.001 and 0.048, respectively), but inversely to the integrity of microvascular basement membrane (r=-0.531, P=0.033).
CONCLUSIONThe 2D-TMAP suggests the overall state of the micro-environment for tumor growth. The 2D-TMAP of NSCLC regulates angiogenesis and tumor cell proliferation through a mesh-like structure, and better understanding of the characteristics and possible mechanism of 2D-TMAP expression can be of great clinical importance.