4.4 Article

Tumor cohesion and glioblastoma cell dispersal

Journal

FUTURE ONCOLOGY
Volume 9, Issue 8, Pages 1121-1132

Publisher

FUTURE MEDICINE LTD
DOI: 10.2217/FON.13.66

Keywords

dispersal velocity; fibronectin matrix assembly; glioblastoma; integrin; matrix stiffness; tissue cohesion; tissue surface tensiometry; wetting

Categories

Funding

  1. NIH [RO1CA118755]

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Patients with glioblastoma typically present when tumors are at an advanced stage. Surgical resection, radiotherapy and adjuvant chemotherapy are currently the standard of care for glioblastoma. However, due to the infiltrative and dispersive nature of the tumor, recurrence rate remains high and typically results in very poor prognosis. Efforts to treat the primary tumor are, therefore, palliative rather than curative. From a practical perspective, controlling growth and dispersal of the recurrence may have a greater impact on disease-free survival. In order for cells to disperse, they must first detach from the mass. Preventing detachment may keep tumors that recur more localized and perhaps more amenable to therapy. Here we introduce a new perspective in which a quantifiable mechanical property, namely tissue surface tension, can provide novel information on tumor behavior. The overall theme of the discussion will attempt to integrate how adhesion molecules can alter a tumor's mechanical properties and how, in turn, these properties can be modified to prevent tumor cell detachment and dispersal.

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