Document Type
Article
Journal Title
Bone Research
Publication Date
2022
Volume
10
Abstract
Bone metastases occur in patients with advanced-stage prostate cancer (PCa). The cell-cell interaction between PCa and the bone microenvironment forms a vicious cycle that modulates the bone microenvironment, increases bone deformities, and drives tumor growth in the bone. However, the molecular mechanisms of PCa-mediated modulation of the bone microenvironment are complex and remain poorly defined. Here, we evaluated growth differentiation factor-15 (GDF15) function using in vivo preclinical PCa-bone metastasis mouse models and an in vitro bone cell coculture system. Our results suggest that PCa-secreted GDF15 promotes bone metastases and induces bone microarchitectural alterations in a preclinical xenograft model. Mechanistic studies revealed that GDF15 increases osteoblast function and facilitates the growth of PCa in bone by activating osteoclastogenesis through osteoblastic production of CCL2 and RANKL and recruitment of osteomacs. Altogether, our findings demonstrate the critical role of GDF15 in the modulation of the bone microenvironment and subsequent development of PCa bone metastasis.
ISSN
2095-4700
DOI Link
Creative Commons License
This work is licensed under a Creative Commons Attribution 4.0 International License.
Recommended Citation
Siddiqui, Jawed A.; Seshacharyulu, Parthasarathy; Muniyan, Sakthivel; Pothuraju, Ramesh; Khan, Parvez; Vengoji, Raghupathy; Chaudhary, Sanjib; Maurya, Shailendra K.; Lele, Subodh M.; Jain, Maneesh; Datta, K; Nasser, Mohd W.; and Batra, Surinder K., "GDF15 Promotes Prostate Cancer Bone Metastasis and Colonization Through Osteoblastic CCL2 and RANKL Activation" (2022). Journal Articles: Biochemistry & Molecular Biology. 151.
https://digitalcommons.unmc.edu/com_bio_articles/151
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