Contact Info

Kelley S. Madden, Ph.D. Department of Biomedical Engineering University of Rochester work Box 603 601 Elmwood Ave Rochester, NY 14642 office: MC 5-7220 p +1-585-273-5724 f +1-585-276-2254

Recent Publications

    • Bellinger DL
    • Stevens SY
    • Thyaga Rajan S
    • Lorton D
    • Madden KS
    (2005 Jul 11). Aging and sympathetic modulation of immune function in Fischer 344 rats: effects of chemical sympathectomy on primary antibody response. J Neuroimmunol. 165, 21-32.
    • Kohut ML
    • Senchina DS
    • Madden KS
    • Martin AE
    • Felten DL
    • Moynihan JA
    (2004 Oct 18). Age effects on macrophage function vary by tissue site, nature of stimulant, and exercise behavior. Exp Gerontol. 39, 1347-60.
    • Madden KS
    (2003 Mar 04). Catecholamines, sympathetic innervation, and immunity. Brain Behav Immun. 17 Suppl 1, S5-10.
See all

Kelley S. Madden

Photo of Kelley Madden
  • Research Assistant Professor

    • Biomedical Engineering

Brown Lab

Research Overview

In breast cancer patients, chronic emotional stress is an unfortunate accompaniment to the physiological toll of the cancer itself. In laboratory animals, exposure to stressful situations, such as surgery, social isolation, or restraint, can accelerate tumor growth, but the biological mechanisms are not clear. We propose that release of norepinephrine, a sympathetic nervous system neurotransmitter released by stressor exposure, can promote tumor growth by facilitating the growth of new tumor blood vessels (angiogenesis). We will examine the role sympathetic nervous system activation plays in tumor pathology by assessing angiogenesis, and pro-angiogenenic pathways in vitro and in vivo. These experiments take advantage of a unique combination of abilities and interests in our laboratory, including expertise in the neuroendocrine response to stress, as well as an established research program pioneering the use of powerful new microscope technologies to study tumor biology in general and breast cancer angiogenesis in particular. Our results will provide insight into the role that stress plays in breast tumor growth and will begin to elucidate the underlying mechanisms. These experiments will also lay the foundation for future experiments studying how stress-induced neurotransmitters and hormones signal malignant and host cells and influence tumor growth. Inhibiting the host stress response may be an additional tool to retard breast cancer growth in humans