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Biomedical subjects

L Haney

Publications and source records attributed to L Haney.

21 records · Page 2Linked to original sources

Cytogenetic analysis of collagenase- releasing rabbit VX-2 carcinoma-derived cells.

Primary cultures of rabbit VX-2 carcinoma appeared to be heterogeneous, containing at least two morphologically distinct cell types, fibroblast-like cells (F cells) and epithelioid cells (E cells). Ultrastructural studies suggested that the E cells were of epithelial origin, whereas the F cells did not differ significantly from normal rabbit fibroblasts. Cytogenetic studies showed that the E cells were characterized by numerical and structural chromosomal changes which remained constant subsequent to serial in vitro culture and in vivo transplants in rabbits. Analysis of G-banded chromosomes from E cells revealed a modal number of 54 with relatively few normal chromosomes and a variety of distinctive, mostly unidentifiable marker chromosomes. The origin of only four marker chromosomes could be partially determined. The ratio of normal to marker chromosomes remained relatively constant following serial transplants in rabbits. The F cells appeared to be derived mainly from host tissue, as they contained a normal diploid complement with sex chromosomes corresponding to the sex of the host.

Animals↗

Host-mediated effectors of tumor invasion: role of mast cells in matrix degradation.

The role of collagenolytic enzymes in tumor invasion and metastasis has been emphasized, but the source of enzyme activity has remained unclear. Degradation of stromal connective tissue is a common feature of invasive neoplasia, and host-tumor cell interactions are probably important for localized collagenolysis. We have examined the role of mast cells in malignant cell invasion using cells derived from the rat mammary adenocarcinoma 13762NF. Histologic studies have shown increased numbers of mast cells at the zone of tumor invasion. Mast cell products and conditioned medium from such cells stimulated the production of collagenolytic enzymes by stromal fibroblasts as well as certain subpopulations of tumor cells in vitro. The tumor cell response to mast cell-mediated stimulation of collagenolysis appears to be related to the metastatic potential of the tumor cell. A subpopulation of host fibroblasts derived from the invading tumor zone was also found to be more responsive to mast cell factors than normal fibroblasts, as judged by collagenase production. Thus the mast cell has the potential to induce collagenolytic activity from both host fibroblasts and tumor cells.

Adenocarcinoma↗