Part of the multiple myeloma-associated microvessels is functionally connected to the systemic circulation: a study in the murine 5T33MM model

Virchows Archiv : an International Journal of Pathology
Hendrik De RaeveKarin Vanderkerken

Abstract

It is now well established that angiogenesis in multiple myeloma (MM) is associated with poor prognosis. The exact function of the newly formed vessels in MM is, however, a matter of debate. It is believed that, in contrast to solid tumor growth, the bone marrow (BM) is a sufficiently vascularized organ to support expansion of the MM clone with no need for additional blood vessels. From this point of view, it could be that MM-associated angiogenesis is rather an epiphenomenon and that the newly formed microvessels form a chaotic network that does not contribute to the blood flow. We investigated whether these newly formed microvessels in MM are connected to the blood circulation. The intravenously injected ferritin 30 min prior to sacrifice was detected in 100% of the BM vessels of control mice. In MM-bearing mice, the ferritin tracer was found in 31% of the MM-associated vessels, indicating a connection with the peripheral blood circulation in these vessels. We conclude that, comparable to the situation in solid tumors, at least part of the tumor-associated microvessels in MM is functionally connected to the blood circulation and, therefore, can participate in the transport of nutrients and in the dissemination of MM cells.

References

Jul 1, 1994·British Journal of Haematology·A VaccaF Dammacco
Mar 5, 2002·British Journal of Cancer·E Van ValckenborghK Vanderkerken
Sep 19, 2002·International Journal of Cancer. Journal International Du Cancer·Els Van ValckenborghKaren Vanderkerken
Jan 22, 2003·Microvascular Research·Francesco MollicaPaolo A Netti
Jul 12, 2003·Blood·Angelo VaccaFranco Dammacco

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Citations

Jun 3, 2011·Mathematical Biosciences and Engineering : MBE·Ariosto SilvaRobert Gatenby

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