The accomplishment of malignant growth immunotherapy on acknowledgment checkpoints for killing diseased cells has raised an incredible enthusiasm of researchers in seeing new and old techniques for immunotherapeutic. CD47 (a group of separation 47) is a cell surface glycoprotein and generally communicated on cells, which has a place with the immunoglobulin (Ig) superfamily as a cell film receptor that serves in resistant treatment. CD47 is an inhibitory receptor communicated on the tumor cell surface and collaborates with signal receptor protein-alpha (SIPR-α, likewise named CD172a or SHPS-1), which may escape from resistant cells, for example, macrophage and T cells. Then, tumor cells express high CD47 protein, which may emit exosomes with high CD47 articulation. The high CD47 articulation exosomes could serve the tumor metastasis procedure and give move comfort to tumors on the microenvironment. CD47 on diseased cells can likewise influence the movement and intrusion of cells. The high CD47 articulation on tumor or CTC (flowing tumor cell) surface methods the more grounded relocation and attack and makes them escape from insusceptible cells for phagocytosis, for example, T cells, NK (characteristic executioner) cells, and macrophage, which could be utilized for conclusion and forecast on malignant growth patients. Then, focusing on CD47 joined with different biomarkers, for example, EpCAM (epithelial cell grip particle), CD44, and so on malignancy surface could be utilized to disengage CTCs from patients’ blood. As far as treatment, hostile to CD47 counteracting agent joined with another immunizer, for example, against PD-L1 (customized passing ligand 1) neutralizer or medications, for example, rituximab, DOX or oxaliplatin likewise has better restorative impacts and antitumor capacity to tumors. Utilizing nanomaterials as a delegate for CD47-related resistant treatment could significantly expand the restorative impact and conquer numerous natural hindrances for hostile to CD47 counteracting agents in vivo. In this audit, we examine the significant job and the capacity of CD47 in tumor metastasis and furthermore give a reference to related research.