Growing evidence has confirmed that the activation of SDF-1α/CXCR4 signaling promotes tumor cell proliferation, migration, survival, gene transcription, and blockade of the SDF-1α/CXCR4 axis reverses this phenomenon and results in cell cycle arrest, apoptosis, and the inhibition of downstream signaling [6,13,14,15]. Here, CXCL12 is linked to neoplasm.