Crosstalk between bone metastatic cancer cells and sensory nerves in bone metastatic progression

Author:

Park Sun H1ORCID,Tsuzuki Shunsuke12ORCID,Contino Kelly F1ORCID,Ollodart Jenna1ORCID,Eber Matthew R1,Yu Yang1,Steele Laiton R1ORCID,Inaba Hiroyuki2,Kamata Yuko3,Kimura Takahiro2,Coleman Ilsa4,Nelson Peter S4,Muñoz-Islas Enriqueta5,Jiménez-Andrade Juan Miguel5,Martin Thomas J6,Mackenzie Kimberly D7,Stratton Jennifer R7,Hsu Fang-Chi8,Peters Christopher M6,Shiozawa Yusuke1ORCID

Affiliation:

1. Department of Cancer Biology and Atrium Health Wake Forest Baptist Comprehensive Cancer Center, Wake Forest University School of Medicine, Winston-Salem, NC, USA

2. Department of Urology, Jikei University School of Medicine, Tokyo, Japan

3. Department of Oncology, Jikei University School of Medicine, Tokyo, Japan

4. Division of Human Biology, Fred Hutchinson Cancer Center, Seattle, WA, USA

5. Unidad Académica Multidisciplinaria Reynosa Aztlán, Universidad Autónoma de Tamaulipas, Reynosa, Mexico

6. Department of Anesthesiology, Wake Forest University School of Medicine, Winston-Salem, NC, USA

7. Teva Pharmaceuticals

8. Department of Biostatistics and Data Science Wake Forest University School of Medicine, Winston-Salem, NC, USA

Abstract

Although the role of peripheral nerves in cancer progression has been appreciated, little is known regarding cancer/sensory nerve crosstalk and its contribution to bone metastasis and associated pain. In this study, we revealed that the cancer/sensory nerve crosstalk plays a crucial role in bone metastatic progression. We found that (i) periosteal sensory nerves expressing calcitonin gene–related peptide (CGRP) are enriched in mice with bone metastasis; (ii) cancer patients with bone metastasis have elevated CGRP serum levels; (iii) bone metastatic patient tumor samples express elevated calcitonin receptor-like receptor (CRLR, a CGRP receptor component); (iv) higher CRLR levels in cancer patients are negatively correlated with recurrence-free survival; (v) CGRP induces cancer cell proliferation through the CRLR/p38/HSP27 pathway; and (vi) blocking sensory neuron–derived CGRP reduces cancer cell proliferation in vitro and bone metastatic progression in vivo. This suggests that CGRP-expressing sensory nerves are involved in bone metastatic progression and that the CGRP/CRLR axis may serve as a potential therapeutic target for bone metastasis.

Funder

HHS | NIH | National Cancer Institute

U.S. Department of Defense

METAvivor

Publisher

Life Science Alliance, LLC

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