Sequential process of blood‐borne lung metastases of spontaneous mammary carcinoma in C3H mice

We examined the correlation between growth characteristics and the incidence of lung metastases of spontaneous mammary tumors in C3H mice. The growth pattern of the mammary tumors was composed of initial rapid growth, declining growth, and further exponential growth (re‐growth). The “re‐growth” was closely associated with loss of differentiation and progressive increase of the incidence of lung metastases. In addition, we observed the sequential process of blood‐borne lung metastases. The findings involved (i) “passive” intravasation: carcinoma nests encased in newly formed endothelial cells are released into sinusoidal vessels within primary tumors; (ii) “mechanical” arrest and proliferation of multicellular tumor emboli in pulmonary arterioles; (iii) “active” extravasation: carcinoma cells rushed out to the lung parenchyma through the arteriolar walls ruptured by initial minimal penetration of carcinoma cells and intravascular pressure. The results indicate a stable progression in the natural history of C3H mouse mammary carcinomas characterized by growth characteristics, the incidence of lung metastases, and histological change generating a poorly differentiated clone which can successfully complete a sequential process of blood‐borne lung metastasis. © 1993 Wiley‐Liss, Inc.

[1]  D. Ingber,et al.  Extracellular matrix as a solid-state regulator in angiogenesis: identification of new targets for anti-cancer therapy. , 1992, Seminars in cancer biology.

[2]  L. Liotta,et al.  Immunohistochemical distribution of type IV collagenase in normal, benign, and malignant breast tissue. , 1990, The American journal of pathology.

[3]  D. Tarin,et al.  Tumor cell dissemination patterns and metastasis of murine mammary carcinoma. , 1989, Cancer research.

[4]  L. Norton A Gompertzian model of human breast cancer growth. , 1988, Cancer research.

[5]  J. Arends,et al.  Type IV collagen immunoreactivity in colorectal cancer: Prognostic value of basement membrane deposition , 1988, Cancer.

[6]  G. Nicolson Cancer metastasis: tumor cell and host organ properties important in metastasis to specific secondary sites. , 1988, Biochimica et biophysica acta.

[7]  K. Dingemans What's new in the ultrastructure of tumor invasion in vivo? , 1988, Pathology, research and practice.

[8]  M. Zeydel,et al.  Collagenase and elastase production by mouse mammary adenocarcinoma primary cultures and cloned cells. , 1986, Cancer research.

[9]  T. Stamey,et al.  PATTERNS OF PROGRESSION IN PROSTATE CANCER , 1986, The Lancet.

[10]  A. Ben-Ze'ev,et al.  Modulation of the metastatic capability in B16 melanoma by cell shape. , 1983, Science.

[11]  G P Siegal,et al.  Loss of basement membrane components by invasive tumors but not by their benign counterparts. , 1983, Laboratory investigation; a journal of technical methods and pathology.

[12]  P. Falk Differences in vascular pattern between the spontaneous and the transplanted C3H mouse mammary carcinoma. , 1982, European journal of cancer & clinical oncology.

[13]  S. Hamamoto,et al.  Basal lamina and tissue recognition in malignant mammary tumors. , 1980, Cancer research.

[14]  D. Tarin,et al.  Metastatic colonization potential of primary tumour cells in mice. , 1979, British Journal of Cancer.

[15]  N. Finlayson,et al.  The resistance of arteries to tumour invasion. , 1965, British Journal of Cancer.

[16]  A. K. Laird Dynamics of Tumour Growth: Comparison of Growth Rates and Extrapolation of Growth Curve to One Cell , 1965, British Journal of Cancer.

[17]  J. Folkman,et al.  Angiogenic factors. , 1987, Science.