TY - JOUR
T1 - Urinary excretion of transforming growth factor-alpha in patients with transitional cell carcinoma
AU - Chow, Nan Haw
AU - Liu, Hsiao Sheng
AU - Chang, Chih Jen
AU - Chi, Yun Chan
AU - Tzai, Tzong Shin
AU - Li, Eric I.C.
AU - Lin, Johnny Shinn Nan
PY - 1998/5
Y1 - 1998/5
N2 - This study was performed to examine the involvement of transforming growth factor-alpha (TGF-α) in urothelial tumorigenesis. TGF-α urine levels were measured in patients with urothelial carcinoma (n = 68), patients who were tumor-free (n = 58), patients with non-neoplastic inflammatory disease (n = 20), and normal controls (n = 39). Both inflammatory and neoplastic urologic diseases had elevated TGF-α urine levels (169.5 ng/gm and 116.7 ng/gm, respectively) as compared to normal controls (39.1 ng/gm)(p = 0.0001). For patients with active cancer, TGF-α levels were positively associated with histologic grading (P = 0.009), nodular shape, and expression of epidermal growth factor receptor in primary tumour (P = 0.03, respectively). But, there was no important relationship with staging classification, number and size of tumor (P > 0.1, respectively). TGF-α urine levels did not correlate with the serum content (n = 26; P > 0.5), or the immunohistochemical expression of TGF-α (n = 60) in corresponding tumor (P > 0.1). Significant factors in predicting patient survival were clinical staging nodular shape and size of tumor (P < 0.05, respectively). Our data implies that interaction of urinary TGF-α/urothelial epidermal growth factor receptor may play a positive role in the carcinogenesis of human urothelium.
AB - This study was performed to examine the involvement of transforming growth factor-alpha (TGF-α) in urothelial tumorigenesis. TGF-α urine levels were measured in patients with urothelial carcinoma (n = 68), patients who were tumor-free (n = 58), patients with non-neoplastic inflammatory disease (n = 20), and normal controls (n = 39). Both inflammatory and neoplastic urologic diseases had elevated TGF-α urine levels (169.5 ng/gm and 116.7 ng/gm, respectively) as compared to normal controls (39.1 ng/gm)(p = 0.0001). For patients with active cancer, TGF-α levels were positively associated with histologic grading (P = 0.009), nodular shape, and expression of epidermal growth factor receptor in primary tumour (P = 0.03, respectively). But, there was no important relationship with staging classification, number and size of tumor (P > 0.1, respectively). TGF-α urine levels did not correlate with the serum content (n = 26; P > 0.5), or the immunohistochemical expression of TGF-α (n = 60) in corresponding tumor (P > 0.1). Significant factors in predicting patient survival were clinical staging nodular shape and size of tumor (P < 0.05, respectively). Our data implies that interaction of urinary TGF-α/urothelial epidermal growth factor receptor may play a positive role in the carcinogenesis of human urothelium.
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M3 - Article
C2 - 9677466
AN - SCOPUS:0031927665
SN - 0250-7005
VL - 18
SP - 2053
EP - 2057
JO - Anticancer research
JF - Anticancer research
IS - 3 B
ER -