TY - JOUR
T1 - Elevated insulin-like growth factor-1 and insulin-like growth factor binding protein-2 in malignant pleural effusion
AU - Olchovsky, David
AU - Shimon, Ilan
AU - Goldberg, Iris
AU - Shulimzon, Tiberiu
AU - Lubetsky, Aharon
AU - Yellin, Alon
AU - Pariente, Clara
AU - Karasik, Avraham
AU - Kanety, Hannah
PY - 2002
Y1 - 2002
N2 - Insulin-like growth factor-1 (IGF-1) and its binding proteins (IGFBPs) are produced by many tissues and are present in serum and other biological fluids. Alterations in sera of IGF-1 and 2 and IGFBPs were demonstrated in patients with malignancy, infection and other diseases causing pleural effusion. In this study the IGF-1 and IGFBP-2 content and the specific electrophoretic patterns of IGFBPs in samples of sera and pleural effusions of 25 patients with malignancy, infection and congestive heart failure were investigated. IGF-1 levels in exudative effusions of malignant solid tumors were significantly higher [(mean ± SD), 20.9 ± 7.5 nmol/L, n = 9] than in lymphoma (11.0 ± 5.2 nmol/L, n = 5; p < 0.05), infection (11.4 ± 6.5 nmol/L, n = 6; p < 0.05) and transudative effusion of congestive heart failure (4.3 ± 3.3 nmol/L, n = 5; p < 0.02). IGFBP-2 was markedly increased in effusions of malignant solid tumors (2.14 < 0.82 mg/L, n = 9) compared with exudates of lymphoma, infection and transudates (1.10 ± 0.70, 1.22 ± 0.32 and 0.93 ± 0.52 nmol/L, respectively, p < 0.05). Moreover, in effusion of solid tumors, IGFBP-2 levels were higher than those in corresponding sera, which suggests local production of this binding protein. The demonstration of IGFBP-2 in solid tumor cells by immunohistochemistry further supports this possibility. This work demonstrates the existence of the IGF-1/IGFBP system in pleural fluids from different etiologies and implies possible use of IGF-1 and IGFBP-2 as a potential marker of malignant effusions.
AB - Insulin-like growth factor-1 (IGF-1) and its binding proteins (IGFBPs) are produced by many tissues and are present in serum and other biological fluids. Alterations in sera of IGF-1 and 2 and IGFBPs were demonstrated in patients with malignancy, infection and other diseases causing pleural effusion. In this study the IGF-1 and IGFBP-2 content and the specific electrophoretic patterns of IGFBPs in samples of sera and pleural effusions of 25 patients with malignancy, infection and congestive heart failure were investigated. IGF-1 levels in exudative effusions of malignant solid tumors were significantly higher [(mean ± SD), 20.9 ± 7.5 nmol/L, n = 9] than in lymphoma (11.0 ± 5.2 nmol/L, n = 5; p < 0.05), infection (11.4 ± 6.5 nmol/L, n = 6; p < 0.05) and transudative effusion of congestive heart failure (4.3 ± 3.3 nmol/L, n = 5; p < 0.02). IGFBP-2 was markedly increased in effusions of malignant solid tumors (2.14 < 0.82 mg/L, n = 9) compared with exudates of lymphoma, infection and transudates (1.10 ± 0.70, 1.22 ± 0.32 and 0.93 ± 0.52 nmol/L, respectively, p < 0.05). Moreover, in effusion of solid tumors, IGFBP-2 levels were higher than those in corresponding sera, which suggests local production of this binding protein. The demonstration of IGFBP-2 in solid tumor cells by immunohistochemistry further supports this possibility. This work demonstrates the existence of the IGF-1/IGFBP system in pleural fluids from different etiologies and implies possible use of IGF-1 and IGFBP-2 as a potential marker of malignant effusions.
UR - http://www.scopus.com/inward/record.url?scp=0036262590&partnerID=8YFLogxK
U2 - 10.1080/028418602753669571
DO - 10.1080/028418602753669571
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AN - SCOPUS:0036262590
SN - 0284-186X
VL - 41
SP - 182
EP - 187
JO - Acta Oncologica
JF - Acta Oncologica
IS - 2
ER -