Eur Rev Med Pharmacol Sci 2018; 22 (13): 4146-4155
DOI: 10.26355/eurrev_201807_15407

CT quantitative analysis study for angiogenesis, and degree of ischemic necrosis and glucose metabolite in non-small cell lung cancer

M. Jiang, H.-Y. Lu, X.-H. Shan, W. Xu, X.-D. Geng, C. Lu, J.-H. Chen

Department of Radiology, Affiliated People’s Hospital of Jiangsu University, Zhenjiang City, Jiangsu Province, China. xiuhongshan112@163.com


OBJECTIVE: We aimed at exploring the feasibility of noninvasive late arterial phase enhanced CT imaging in evaluating tumor angiogenesis, ischemic necrosis, and glucose metabolism, thereby providing pathological information for the comprehensive treatment plan in non-small cell lung cancer (NSCLC).

PATIENTS AND METHODS: 52 cases of NSCLC were enrolled in this study. The mean ischemia necrosis CT quantitative value (INCTQ) and CT enhanced value (CTe) of the tumor were determined, and the immunohistochemical staining of factors relating to tumor angiogenesis, ischemic necrosis and glucose metabolism, including VEGF, VEGFR-2, HIF-1α, CAIX, GLUT1, and GLUT3, were conducted.

RESULTS: The mean INCTQ values of different expression grades of VEGF, VEGFR-2, HIF-1α, and CAIX have no significant difference, but the mean INCTQ values of different expression grades of GLUT1 or GLUT3 have significant differences (p < 0.001), respectively. However, INCTQ value has a positive correlation with CAIX expression. In addition, CTe value was positively correlated with VEGF.

CONCLUSIONS: To sum up, late arterial phase CT enhanced images of NSCLC not only can assess the tumor angiogenesis, but also can reflect the degree of ischemic necrosis, effectively reflecting the level of glucose metabolism in tumor and tumor angiogenesis, for the comprehensive treatment program.

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To cite this article

M. Jiang, H.-Y. Lu, X.-H. Shan, W. Xu, X.-D. Geng, C. Lu, J.-H. Chen
CT quantitative analysis study for angiogenesis, and degree of ischemic necrosis and glucose metabolite in non-small cell lung cancer

Eur Rev Med Pharmacol Sci
Year: 2018
Vol. 22 - N. 13
Pages: 4146-4155
DOI: 10.26355/eurrev_201807_15407