Tumour regulation of fibroblast hyaluronan expression: a mechanism to facilitate tumour growth and invasion

被引:53
作者
Edward, M
Gillan, C
Micha, D
Tammi, RH
机构
[1] Univ Glasgow, Div Canc Sci & Mol Pathol, Sect Squamous Cell Biol & Dermatol, Glasgow G12 8QQ, Lanark, Scotland
[2] Univ Kuopio, Dept Anat, FIN-70211 Kuopio, Finland
关键词
D O I
10.1093/carcin/bgi064
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
Hyaluronan, a high molecular weight glycosaminoglycan is associated with cellular proliferation and migration. In a number of different tumour types, there is a close correlation between tumour progression and hyaluronan production, either by the tumour cells or the surrounding stromal cells. We have examined the ability of an aggressive melanoma cell line (C8161) to stimulate the synthesis of fibroblast hyaluronan, and the association of cell-surface CD44 receptors and hyaluronan with invasion. Melanoma cell-conditioned medium (CM) prepared in low glucose medium (1 mg/ml) stimulated the synthesis of fibroblast glycosaminoglycan as measured by [H-3] glucosamine incorporation, and the synthesis of hyaluronan as measured using a specific hyaluronan-binding plate assay, while tumour cell-CM prepared in high glucose medium (4.5 mg/ml) inhibited the synthesis of fibroblast glycosaminoglycan. High glucose tumour cell-CM contained large amounts of lactate that appeared to inhibit the tumour-derived factor stimulation of fibroblast glycosaminoglycan synthesis, as removal of the lactate restored the stimulating activity. Melanoma cells seeded on contracted collagen lattices and incubated at the air/liquid interface rapidly formed a multilayered cell mass on the surface, with significant invasion of the gel. Hyaluronan staining was apparent within the collagen gel, and strong staining was seen around the invading tumour cells, but not around those cell layers near the surface. CD44 expression on the tumour cells was confined to those invading cells and corresponded to cellular hyaluronan staining. Hyaluronan staining was also apparent around and between tumour cells invading fibroblast-free collagen lattices. Monolayer cultures of C8161 cells stained strongly for CD44, but few cells stained for hyaluronan, while no detectable hyaluronan was released into the medium. In summary, the C8161 melanoma cells stimulated the synthesis of fibroblast hyaluronan, and in collagen lattices, Only the invasive tumour cells expressed CD44 and hyaluronan, either in the presence or absence of fibroblasts.
引用
收藏
页码:1215 / 1223
页数:9
相关论文
共 40 条
[1]
Anttila MA, 2000, CANCER RES, V60, P150
[2]
Hyaluronan in peritumoral stroma and malignant cells associates with breast cancer spreading and predicts survival [J].
Auvinen, P ;
Tammi, R ;
Parkkinen, J ;
Tammi, M ;
Ågren, U ;
Johansson, R ;
Hirvikoski, P ;
Eskelinen, M ;
Kosma, VM .
AMERICAN JOURNAL OF PATHOLOGY, 2000, 156 (02) :529-536
[3]
INTERACTION BETWEEN CD44 AND HYALURONATE IS DIRECTLY IMPLICATED IN THE REGULATION OF TUMOR-DEVELOPMENT [J].
BARTOLAZZI, A ;
PEACH, R ;
ARUFFO, A ;
STAMENKOVIC, I .
JOURNAL OF EXPERIMENTAL MEDICINE, 1994, 180 (01) :53-66
[4]
INCREASED HYALURONATE SYNTHESIS IS REQUIRED FOR FIBROBLAST DETACHMENT AND MITOSIS [J].
BRECHT, M ;
MAYER, U ;
SCHLOSSER, E ;
PREHM, P .
BIOCHEMICAL JOURNAL, 1986, 239 (02) :445-450
[5]
Hyaluronan synthase-3 is upregulated in metastatic colon carcinoma cells and manipulation of expression alters matrix retention and cellular growth [J].
Bullard, KM ;
Kim, HR ;
Wheeler, MA ;
Wilson, CM ;
Neudauer, CL ;
Simpson, MA ;
McCarthy, JB .
INTERNATIONAL JOURNAL OF CANCER, 2003, 107 (05) :739-746
[6]
Functions of hyaluronan in wound repair [J].
Chen, WYJ ;
Abatangelo, G .
WOUND REPAIR AND REGENERATION, 1999, 7 (02) :79-89
[7]
High CD44 surface expression on primary tumours of malignant melanoma correlates with increased metastatic risk and reduced survival [J].
Dietrich, A ;
Tanczos, E ;
Vanscheidt, W ;
Schopf, E ;
Simon, JC .
EUROPEAN JOURNAL OF CANCER, 1997, 33 (06) :926-930
[10]
Lactate-sensitive response elements in genes involved in hyaluronan catabolism [J].
Formby, B ;
Stern, R .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2003, 305 (01) :203-208