Tumor-infiltrating nerves functionally alter brain circuits and modulate behavior in a mouse model of head-and-neck cancer
Jeffrey Barr,
Austin Walz,
Anthony C Restaino,
Moran Amit,
Sarah M Barclay,
Elisabeth G Vichaya,
William C Spanos,
Robert Dantzer,
Sebastien Talbot,
Paola D Vermeer
Affiliations
Jeffrey Barr
Sanford Research, Cancer Biology and Immunotherapies Group, Sioux Falls, Sioux Falls, United States
Austin Walz
Sanford Research, Cancer Biology and Immunotherapies Group, Sioux Falls, Sioux Falls, United States
Anthony C Restaino
Sanford Research, Cancer Biology and Immunotherapies Group, Sioux Falls, Sioux Falls, United States; University of South Dakota, Sanford School of Medicine, Vermillion, United States
University of Texas, MD Anderson Cancer Center, Houston, United States
Sarah M Barclay
Sanford Research, Cancer Biology and Immunotherapies Group, Sioux Falls, Sioux Falls, United States
Elisabeth G Vichaya
Baylor University, Department of Psychology and Neuroscience, Waco, United States
William C Spanos
Sanford Research, Cancer Biology and Immunotherapies Group, Sioux Falls, Sioux Falls, United States; University of South Dakota, Sanford School of Medicine, Vermillion, United States
Sanford Research, Cancer Biology and Immunotherapies Group, Sioux Falls, Sioux Falls, United States; University of South Dakota, Sanford School of Medicine, Vermillion, United States
Cancer patients often experience changes in mental health, prompting an exploration into whether nerves infiltrating tumors contribute to these alterations by impacting brain functions. Using a mouse model for head and neck cancer and neuronal tracing, we show that tumor-infiltrating nerves connect to distinct brain areas. The activation of this neuronal circuitry altered behaviors (decreased nest-building, increased latency to eat a cookie, and reduced wheel running). Tumor-infiltrating nociceptor neurons exhibited heightened calcium activity and brain regions receiving these neural projections showed elevated Fos as well as increased calcium responses compared to non-tumor-bearing counterparts. The genetic elimination of nociceptor neurons decreased brain Fos expression and mitigated the behavioral alterations induced by the presence of the tumor. While analgesic treatment restored nesting and cookie test behaviors, it did not fully restore voluntary wheel running indicating that pain is not the exclusive driver of such behavioral shifts. Unraveling the interaction between the tumor, infiltrating nerves, and the brain is pivotal to developing targeted interventions to alleviate the mental health burdens associated with cancer.