Literature DB >> 6331653

Distinct high-performance liquid chromatography pattern of transforming growth factor activity in urine of cancer patients as compared with that of normal individuals.

E S Kimball, W H Bohn, K D Cockley, T C Warren, S A Sherwin.   

Abstract

Reverse-phase high-performance liquid chromatography (HPLC) performed on urine from cancer patients and normal controls revealed the presence of seven chromatographically distinct peaks of transforming growth factor (TGF) activity, as measured by colony formation of normal rat kidney cells in soft agar. Comparison of urines from normal donors and cancer patients showed no differences in EGF (epidermal growth factor)-dependent beta-TGF-like activity but did reveal distinct patterns of EGF-related, EGF-independent alpha-TGF-like activity. All urine samples contained at least two chromatographically distinguishable forms of EGF-dependent TGF activity, eluting from HPLC as broad peaks with 30 and 43% acetonitrile. The remaining five TGFs eluted as sharp peaks with 32, 34, 35, 37, and 38% acetonitrile, demonstrated EGF-competing activity, and thus were functionally related to EGF. Two of the five EGF-related TGFs were consistently elevated only in the urine of cancer patients and eluted with 32% (TGFA) and 37% (TGFD) acetonitrile Two of the other EGF-related TGFs, eluting with 34% (TGFB) and 35% (TGFC) acetonitrile, were commonly found in both normals and cancer patients. The fifth EGF-related TGF, TGFE, eluting with 38% acetonitrile, was found only in normal donor specimens. TGFA corresponded to the unique Mr 30,000 TGF activity previously identified only in the urine of cancer patients. These observations demonstrate that cancer patients produce high levels of EGF-related TGF activities which can be readily distinguished, using reverse-phase HPLC, from EGF-related TGFs produced by normal individuals. Using a solid-phase competitive radioreceptor binding assay for EGF, we demonstrated that quantitation of EGF-competing activity is as sensitive and effective as the soft-agar colony formation assay for distinguishing HPLC profiles of urinary TGF from cancer patients versus that from normal individuals.

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Year:  1984        PMID: 6331653

Source DB:  PubMed          Journal:  Cancer Res        ISSN: 0008-5472            Impact factor:   12.701


  8 in total

1.  Hormones in breast fluid.

Authors:  D P Rose
Journal:  Breast Cancer Res Treat       Date:  1986       Impact factor: 4.872

2.  Characterization of a newly established human urinary bladder cancer cell line (BT-1).

Authors:  W Heckl; J Köhler; H Hoehn; J Dämmrich
Journal:  Urol Res       Date:  1988

3.  Expression of growth factors and receptors during specific phases in regenerating urothelium after acute injury in vivo.

Authors:  W I de Boer; A G Schuller; M Vermey; T H van der Kwast
Journal:  Am J Pathol       Date:  1994-11       Impact factor: 4.307

4.  Immunological detection and quantitation of alpha transforming growth factors in human breast carcinoma cells.

Authors:  I Perroteau; D Salomon; M DeBortoli; W Kidwell; P Hazarika; R Pardue; J Dedman; J Tam
Journal:  Breast Cancer Res Treat       Date:  1986       Impact factor: 4.872

5.  Ectopic peptides released by a human melanoma cell line that modulate the transformed phenotype.

Authors:  J E De Larco; D A Pigott; J A Lazarus
Journal:  Proc Natl Acad Sci U S A       Date:  1985-08       Impact factor: 11.205

6.  Hyperplasia of epithelium adjacent to transitional cell carcinoma can be induced by growth factors through paracrine pathways.

Authors:  W I de Boer; J M Rebel; C D Thijssen; M Vermeij; A J van den Eijnden-Van Raaij; T H van der Kwast
Journal:  Virchows Arch       Date:  1994       Impact factor: 4.064

Review 7.  Mitogenic regulation of normal and malignant breast epithelium.

Authors:  M E Lippman; R B Dickson
Journal:  Yale J Biol Med       Date:  1989 Sep-Oct

8.  Growth factors in ovarian cancer.

Authors:  O J Owens; C Stewart; R E Leake
Journal:  Br J Cancer       Date:  1991-12       Impact factor: 7.640

  8 in total

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