Literature DB >> 7514953

Assessment of urinary beta-core fragment of human chorionic gonadotropin as a new tumor marker of lung cancer.

M Yoshimura1, R Nishimura, A Murotani, Y Miyamoto, T Nakagawa, K Hasegawa, T Koizumi, K Shii, S Baba, N Tsubota.   

Abstract

BACKGROUND: Some patients with lung cancer have been found to have elevated 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 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 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-beta 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 (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 beta-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 II to 62.5% (20 of 32) in Stage III 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. The author were encouraged that there was no significant difference in the positive rates of urinary beta-CF between two major types of lung cancer: adenocarcinoma (49.2%) and SCC (45.2%). Immunohistochemical study revealed positive staining of IR-beta in the cancer tissues from 5 of 12 patients with 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 of IR-beta by lung cancer is not rare, and urinary beta-CF might be a potential tumor marker of lung cancer.

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Year:  1994        PMID: 7514953     DOI: 10.1002/1097-0142(19940601)73:11<2745::aid-cncr2820731116>3.0.co;2-v

Source DB:  PubMed          Journal:  Cancer        ISSN: 0008-543X            Impact factor:   6.860


  5 in total

1.  Ligand-induced receptor dimerization may be critical for signal transduction by choriogonadotropin.

Authors:  N Grewal; S Nagpal; G B Chavali; S S Majumdar; R Pal; D M Salunke
Journal:  Biophys J       Date:  1997-09       Impact factor: 4.033

Review 2.  High level of beta-hCG simulating pregnancy in recurrent osteosarcoma: case report and review of literature.

Authors:  B Leidinger; S Bielack; G Koehler; V Vieth; W Winkelmann; G Gosheger
Journal:  J Cancer Res Clin Oncol       Date:  2004-03-24       Impact factor: 4.553

3.  Urinary gonadotropin peptide (UGP) in Egyptian patients with benign and advanced malignant urological disease.

Authors:  O el-Ahmady; A B Halim; O Mansour; T Salman; A G el-Din; R P Walker
Journal:  Br J Cancer       Date:  1996-06       Impact factor: 7.640

4.  Gonadotropin-mediated chemoresistance: Delineation of molecular pathways and targets.

Authors:  Suchismita Sahoo; Poonam Singh; Beneeta Kalha; Om Singh; Rahul Pal
Journal:  BMC Cancer       Date:  2015-11-25       Impact factor: 4.430

5.  Combination assay of urinary beta-core fragment of human chorionic gonadotropin with serum tumor markers in gynecologic cancers.

Authors:  M Kinugasa; R Nishimura; T Koizumi; K Morisue; T Higashida; T Natazuka; T Nakagawa; T Isobe; S Baba; K Hasegawa
Journal:  Jpn J Cancer Res       Date:  1995-08
  5 in total

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