Int J Biol Sci 2024; 20(4):1297-1313. doi:10.7150/ijbs.91925 This issue Cite

Research Paper

GALNT12 suppresses the bone-specific prostate cancer metastasis by activating BMP pathway via the O-glycosylation of BMPR1A

Yang Yang1#, Meng Ding1#, Haoli Yin2#, Wei Chen1, Hongwei Shen1, Wenli Diao1, Lin Yang1, Haixiang Qin1, Weidong Gan1✉, Xuefeng Qiu1✉, Hongqian Guo1✉

1. Department of Urology, Drum Tower Hospital, Medical School of Nanjing University, Institute of Urology, Nanjing University, China.
2. Department of Urology, The Third Affiliated Hospital of Kunming Medical University, Tumor Hospital of Yunnan Province, Kunming, China.
# Y.Y., M.D. and H.Y. contributed equally to this work.

Citation:
Yang Y, Ding M, Yin H, Chen W, Shen H, Diao W, Yang L, Qin H, Gan W, Qiu X, Guo H. GALNT12 suppresses the bone-specific prostate cancer metastasis by activating BMP pathway via the O-glycosylation of BMPR1A. Int J Biol Sci 2024; 20(4):1297-1313. doi:10.7150/ijbs.91925. https://www.ijbs.com/v20p1297.htm
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Abstract

Graphic abstract

Bone metastasis caused the majority death of prostate cancer (PCa) but the mechanism remains poorly understood. In this present study, we show that polypeptide N-acetylgalactosaminyltransferase 12 (GALNT12) suppresses bone-specific metastasis of PCa. GALNT12 suppresses proliferation, migration, invasion and cell division ability of PCa cells by activating the BMP pathway. Mechanistic investigations showed that GALNT12 augments the O-glycosylation of BMPR1A then actives the BMP pathway. Activated BMP signaling inhibits the expression of integrin αVβ3 to reduce the bone-specific seeding of PCa cells. Furthermore, activated BMP signaling remolds the immune microenvironment by suppressing the STAT3 pathway. Our results of this study illustrate the role and mechanism of GALNT12 in the process of bone metastasis of PCa and identify GALNT12 as a potential therapeutic target for metastatic PCa.

Keywords: prostate cancer, bone metastasis, O-glycosylation, GALNT12, BMPR1A


Citation styles

APA
Yang, Y., Ding, M., Yin, H., Chen, W., Shen, H., Diao, W., Yang, L., Qin, H., Gan, W., Qiu, X., Guo, H. (2024). GALNT12 suppresses the bone-specific prostate cancer metastasis by activating BMP pathway via the O-glycosylation of BMPR1A. International Journal of Biological Sciences, 20(4), 1297-1313. https://doi.org/10.7150/ijbs.91925.

ACS
Yang, Y.; Ding, M.; Yin, H.; Chen, W.; Shen, H.; Diao, W.; Yang, L.; Qin, H.; Gan, W.; Qiu, X.; Guo, H. GALNT12 suppresses the bone-specific prostate cancer metastasis by activating BMP pathway via the O-glycosylation of BMPR1A. Int. J. Biol. Sci. 2024, 20 (4), 1297-1313. DOI: 10.7150/ijbs.91925.

NLM
Yang Y, Ding M, Yin H, Chen W, Shen H, Diao W, Yang L, Qin H, Gan W, Qiu X, Guo H. GALNT12 suppresses the bone-specific prostate cancer metastasis by activating BMP pathway via the O-glycosylation of BMPR1A. Int J Biol Sci 2024; 20(4):1297-1313. doi:10.7150/ijbs.91925. https://www.ijbs.com/v20p1297.htm

CSE
Yang Y, Ding M, Yin H, Chen W, Shen H, Diao W, Yang L, Qin H, Gan W, Qiu X, Guo H. 2024. GALNT12 suppresses the bone-specific prostate cancer metastasis by activating BMP pathway via the O-glycosylation of BMPR1A. Int J Biol Sci. 20(4):1297-1313.

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