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Table 3 Prognostic protein biomarkers for BCBM

From: Predictive and prognostic biomarkers of bone metastasis in breast cancer: current status and future directions

Biomarker

Increased or decreased

Clinical samples

Potential molecular mechanism

Refs.

PAK4

Increased

187 NMBC patients

95 BMBC patients

nPAK4 inhibits LIFR and promotes osteolytic bone destruction in ERα-positive breast cancer

[78]

CAPG, GIPC1

Increased

724 breast cancer patients from AZURE trial

CAPG promotes cell migration and invasion

GIPC1 regulates cell cycle, cell adhesion, and motility

[79, 82, 83]

DOCK4

Increased

689 breast cancer patients from AZURE trial

DOCK4 regulates breast cancer cell migration and metastasis

[84, 85]

RANKL

Increased

413 breast cancer patients

RANKL enhances invasion and metastasis of breast cancer and regulates bone microenvironment

[87, 88]

PRLR

Increased

134 breast cancer patients

PRL promotes the secretion of SHH by breast cancer cells, facilitating osteolysis and increasing invasiveness

[89, 91]

IL-1B

Increased

150 stage II/III primary breast cancer patients

IL-1B promotes EMT in breast cancer cells, enhancing their invasive capacity

[62, 92,93,94]

SCUBE2

Increased

Blood samples from 23 breast cancer patients without distant recurrence, 13 cases with bone metastasis

SCUBE2 regulates the immunosuppressive osteogenic microenvironment

[28]

CTX, ICTP, P1NP

Increased

872 breast cancer patients from AZURE trial

164 pre-treatment stage I-III breast cancer patients

CTX, ICTP and P1NP are associated with bone remodeling

[96, 97]