The P chain of human chorionic gonadotropin (hCG) hormone is produced by fetal cells, gonadal cell tumors and several types of non-gonadal carcinoma. hCG is composed of an Q and a P chain, the latter of which can be used to distinguish the molecule from other related gonadotropin hormones. Detection
Assessment of urinary β-core fragment of human chorionic gonadotropin as a new tumor marker of lung cancer
✍ Scribed by Masahiro Yoshimura; Ryuichiro Nishimura; Akihiro Murotani; Yoshifumi Miyamoto; Toshitaro Nakagawa; Kazuo Hasegawa; Tamio Koizumi; Kouzui Shii; Shigeaki Baba; Noriaki Tsubota
- Publisher
- John Wiley and Sons
- Year
- 1994
- Tongue
- English
- Weight
- 710 KB
- Volume
- 73
- Category
- Article
- ISSN
- 0008-543X
No coin nor oath required. For personal study only.
✦ Synopsis
Background. Some patients with lung cancer have been found to have elevated levels of serum immunoreactive human chorionic gonadotropin (hCG)/hCG@ (IR-@), but it is uncertain whether it would be valuable as a tumor marker. Recently, IR-@ has been demonstrated to consist of at least three different molecules, intact hCG, free hCG@, and hCGB-core fragment (8-CF), in body fluids. In this study, the authors qualitatively analyzed IR-@ in the serum and urine of patients with lung cancer and assessed its clinical usefulness as a tumor marker.
Methods. Highly sensitive and specific enzyme immunoassays were established to measure intact hCG, free hCGj3, and 8-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-8 in the urine, although only 12 had elevated values of IR-@ in the serum. The greater part of the elevated urinary IR-/3 was identified to be @-CF by gel chromatography on Sephadex G-100 (Pharmacia 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 positive rate of urinary @.CF for lung cancer was 48.5% (48 of 99 patients). 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 I1 to 62.5% (20 of 32) in Stage 111 and 72.7% (8 of 11) in Stage IV. These positive rates exceeded or equaled those of the serum tumor markers, carcinoembryonic antigen, and squamous cell carcinoma (SCC)-related antigen, measured simultaneously in the same patients.
📜 SIMILAR VOLUMES
## Abstract Transforming growth factor β1 (TGF‐β1) is thought to be involved in cancer growth and progression. TGF‐β1 changes to its active form after being secreted in its latent form. Our aim was to clarify the significance of plasma concentrations of active and total TGF‐β1 of patients with colo
Background. Small cell lung cancer (SCLC) is distinguished from other histologic types of lung cancer by possessing a variety of neuroendocrine properties. Neuron-specific enolase (NSE) is the most frequently elevated tumor marker for patients with SCLC at diagnosis. To assess the value of neural ce