Mammary carcinoma cell lines of high and low metastatic potential differ not in extravasation but in subsequent migration and growth
VL Morris, S Koop, IC MacDonald, EE Schmidt… - Clinical & experimental …, 1994 - Springer
VL Morris, S Koop, IC MacDonald, EE Schmidt, M Grattan, D Percy, AF Chambers…
Clinical & experimental metastasis, 1994•SpringerWe examined the extravasation and subsequent migration and growth of murine mammary
tumor cell lines (D2A1 and D2. OR) which differ in their metastatic ability in lung and liver,
invasiveness in vitro and expression of the cysteine proteinase cathepsin L. In light of the
differences in invasiveness and cathepsin L expression, we hypothesized that during
hematogenous metastasis the two cell lines would differ primarily in their ability to
extravasate. We used in vivo videomicroscopy of mouse liver and chick embryo …
tumor cell lines (D2A1 and D2. OR) which differ in their metastatic ability in lung and liver,
invasiveness in vitro and expression of the cysteine proteinase cathepsin L. In light of the
differences in invasiveness and cathepsin L expression, we hypothesized that during
hematogenous metastasis the two cell lines would differ primarily in their ability to
extravasate. We used in vivo videomicroscopy of mouse liver and chick embryo …
Abstract
We examined the extravasation and subsequent migration and growth of murine mammary tumor cell lines (D2A1 and D2.OR) which differ in their metastatic ability in lung and liver, invasiveness in vitro and expression of the cysteine proteinase cathepsin L. In light of the differences in invasiveness and cathepsin L expression, we hypothesized that during hematogenous metastasis the two cell lines would differ primarily in their ability to extravasate. We used in vivo videomicroscopy of mouse liver and chick embryo chorioallantoic membrane to examine the process and timing of extravasation and subsequent steps in metastasis for these cell lines. In contrast to our expectations, no differences were found between the cell lines in either the timing or mechanism of extravasation, at least 95% of cells having extravasated by 3 days after injection. However, after extravasation, the more metastatic and invasive D2A1 cells showed a greater ability to migrate to sites which favor tumor growth and to replicate to form micrometastases. These studies point to post-extravasation events (migration and growth) as being critical in metastasis formation.
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