Bone metastasis (BM) may occur in any type of cancer. The diagnosis of patients with BM has increased due to improved imaging technologies and advances in cancer drug therapy that have prolonged the survival time of cancer patients. BM may be asymptomatic in the early stages; however, as the disease progresses, it causes pain, fracture, neurological symptoms associated with spinal cord compression, hypercalcemia, and other specific symptoms that significantly impair the patient's quality of life (QOL). Imaging modalities have disadvantages, such as high cost, radiation exposure, and bone pain associated with holding posture for imaging test; further, they are time-consuming. Hence, patients with BM require convenient and useful biomarkers. However, no blood biomarkers generally useful for diagnosis and therapeutic monitoring of BM are established. Prostate cancer (PC) and breast cancer, in particular, are among the most prone to BM because BM occurs in approximately 70% of patients with advanced disease. Herein, we reviewed various potential bone turnover markers and liquid biopsy for diagnosis and prognosis prediction in patients with BM of PC based on PubMed literature search. The usefulness of conventional bone turnover markers of BM in PC is limited, and cut-off values vary. In the future, the creation of algorithms using these conventional markers and multiple tests, such as liquid biopsy and imaging tests, will help to develop highly accurate techniques for the diagnosis of BM.The number of cancer survivors is increasing due to advances in medical technology, and an increase in effectively diagnosing patients with bone metastasis (BM) (1). The incidence of BM varies depending on the primary tumor type, with prostate cancer (PC) at highest risk of developing BM (85%), followed by lung cancer, kidney cancer, and breast cancer, and it is the lowest (13%) for colon cancer (2-4). Although prostate specific antigen screening and new advances in PC treatment improved survival, future projections indicate that by 2040, 379,000 people will die due to PC worldwide (5). Owing to the progression of systematic medical therapies, life expectancy and the number of patients with BM are increasing and will continue to do so (6). Generally, BM may cause skeletal related events (SRE), such as pain, fractures, spinal cord compressions, hypercalcemia, prolonged hospitalization period, and significantly reduce the quality of life (QOL) in patients with short prognosis (7). BM in patients with breast cancer is a mixed osteolytic and osteoblastic type, whereas in PC, it is predominantly osteosclerotic type. Bone metastatic sites of PC undergo osteogenic changes but are more brittle than normal bone (8). Thus, BM is a clinically important and distinctive condition; however, the American Society of Clinical Oncology guidelines state that there are no established bone turnover markers, effective for monitoring BM in clinical practice (9).In 1889, Paget proposed the seed and soil theory (10), in which cancer cells and remote organs of...