ASSESSMENT OF URINARY BETA-CORE FRAGMENT OF HUMAN CHORIONIC-GONADOTROPIN AS A NEW TUMOR-MARKER OF LUNG-CANCER

Citation
M. Yoshimura et al., ASSESSMENT OF URINARY BETA-CORE FRAGMENT OF HUMAN CHORIONIC-GONADOTROPIN AS A NEW TUMOR-MARKER OF LUNG-CANCER, Cancer, 73(11), 1994, pp. 2745-2752
Citations number
25
Categorie Soggetti
Oncology
Journal title
CancerACNP
ISSN journal
0008543X
Volume
73
Issue
11
Year of publication
1994
Pages
2745 - 2752
Database
ISI
SICI code
0008-543X(1994)73:11<2745:AOUBFO>2.0.ZU;2-9
Abstract
Background. Some patients with lung cancer have been found to have ele vated levels of serum immunoreactive human chorionic gonadotropin (hCG )/hCG beta (IR-beta), but it is uncertain whether it would be valuable as a tumor marker. Recently, IR-beta has been demonstrated to consist of at least three different molecules, intact hCG, free hCG beta, and hCG beta-core fragment (beta-CF), in body fluids. In this study, the authors qualitatively analyzed IR-beta in the serum and urine of patie nts with lung cancer and assessed its clinical usefulness as a tumor m arker. Methods. Highly sensitive and specific enzyme immunoassays were established to measure intact hCG, free hCG beta, and beta-CF in the serum and urine of patients with lung cancer. Results. Of 99 patients with lung cancer, almost half of the patients achieved positive values of IR-beta in the urine, although only 12 had elevated values of IR-b eta in the serum. The greater part of the elevated urinary IR-beta was identified to be beta-CF by gel chromatography on Sephadex G-100 (Pha rmacia LKB Biotechnology, Tokyo, Japan), leading the authors to assess its usefulness as a tumor marker for lung cancer. Based on the cutoff value (0.2 ng/ mg of creatinine) from healthy subjects, the overall p ositive rate of urinary beta-CF for lung cancer was 48.5% (48 of 99 pa tients). The incidence of the marker increased with stage of disease, from 35.7% (15 of 42) in Stage I and 35.7% (5 of 14) in Stage II to 62 .5% (20 of 32) in Stage III and 72.7% (8 of 11) in Stage IV, These pos itive rates exceeded or equaled those of the serum tumor markers, carc inoernbryonic antigen, and squamous cell carcinoma (SCC)-related antig en, measured simultaneously in the same patients. The author were enco uraged that there was no significant difference in the positive rates of urinary beta-CF between two major types of lung cancer: adenocarcin oma (49.2%) and SCC (45.2%). Immunohistochemical study revealed positi ve staining of IR-beta in the cancer tissues from 5 of 12 patients wit h elevated levels of IR-beta, in which most of the positive cases had the elevated levels of serum free hCG beta (>0.5 ng/ml) and/or urinary beta-CF (>1.0 ng/mg of creatinine). Conclusions. Ectopic production o f IR-beta by lung cancer is not rare, and urinary beta-CF might be a p otential tumor marker of lung cancer.