Micro-environmental mechanical stress controls tumor spheroid size and morphology by suppressing proliferation and inducing apoptosis in cancer cells

• Published in: PloS one 2009-02, Vol.4 (2), p.e4632
• Main Authors: Cheng, Gang, Tse, Janet, Jain, Rakesh K, Munn, Lance L
• Format: Article
• Language: English
• Subjects: Angiogenesis; Animals; Apoptosis; Base Sequence; Beads; Biology; Cancer; Cancer cells; Cell Biology/Cellular Death and Stress Responses; Cell Biology/Extra-Cellular Matrix; Cell Biology/Morphogenesis and Cell Biology; Cell death; Cell growth; Cell Proliferation; Cell Shape; Compressive properties; Confining; Confocal; Confocal microscopy; DNA Primers; Dormancy; Drosophila; Fluorescence; Gels; Insects; Laboratories; Mammary Neoplasms, Experimental - pathology; Medical schools; Mice; Microscopy; Microscopy, Confocal; Mitochondria; Morphology; Oncology; Oncology/Breast Cancer; Polymerase Chain Reaction; Regulation; Sepharose; Spatial distribution; Spheroids; Stress; Stress analysis; Stress concentration; Stress distribution; Stress, Mechanical; Studies; Tumor Cells, Cultured; Tumors
• ISSN: 1932-6203; 1932-6203
• DOI: 10.1371/journal.pone.0004632

Compressive mechanical stress produced during growth in a confining matrix limits the size of tumor spheroids, but little is known about the dynamics of stress accumulation, how the stress affects cancer cell phenotype, or the molecular pathways involved. We co-embedded single cancer cells with fluorescent micro-beads in agarose gels and, using confocal microscopy, recorded the 3D distribution of micro-beads surrounding growing spheroids. The change in micro-bead density was then converted to strain in the gel, from which we estimated the spatial distribution of compressive stress around the spheroids. We found a strong correlation between the peri-spheroid solid stress distribution and spheroid shape, a result of the suppression of cell proliferation and induction of apoptotic cell death in regions of high mechanical stress. By compressing spheroids consisting of cancer cells overexpressing anti-apoptotic genes, we demonstrate that mechanical stress-induced apoptosis occurs via the mitochondrial pathway. Our results provide detailed, quantitative insight into the role of micro-environmental mechanical stress in tumor spheroid growth dynamics, and suggest how tumors grow in confined locations where the level of solid stress becomes high. An important implication is that apoptosis via the mitochondrial pathway, induced by compressive stress, may be involved in tumor dormancy, in which tumor growth is held in check by a balance of apoptosis and proliferation.