The M2 TAMs can directly activate angiogenesis through the release of VEGF, bFGF, and PlGF or indirectly activate angiogenesis through the release of matrix metalloproteinases (MMPs) to remodel the extracellular matrix and to improve the migration of endothelial cells (47), which could form new blood vessels and accelerate tumor progression. The gene discussed is FGF2; the disease is neoplasm.