TABLE 2.
Platelet inhibitors | Detailed introduction | Mechanism | Reference |
---|---|---|---|
FAK inhibitors | FAK in platelets was demonstrated to be a promising target, further causing the platelet−tumor interaction | Controlling the platelet extravasation | 183 |
ADP/MMP‐2 inhibitors | ADP and MMP‐2 released from tumor cells | Reducing the activation and aggregation of platelets | 184 |
PTAFR inhibitors | The receptor of platelet‐activating factor (PAF). PAF can activate the platelets | Blocking PAF/PTAFR pathway | 185 |
α‐Hederin | Expression of matrix metalloproteinase‐2 can be hampered by α‐Hederin | Inhibiting the activation of STAT3 | 185 |
PDGFR inhibitors | PDGFR expressed in the tumor cells | Inhibiting PDGFRα/β kinases | 186 , 187 |
Imatinib | Inhibit PDGFRα/Akt and disrupting the action of PDGF | Tyrosine kinase inhibitor | 188 |
HIF1α | Inhibiting the expression of PDGFR in tumor cells | Inhibitor echinomycin | 190 |
Eptifibatide | PD‐L1 inhibitor | Immune checkpoint inhibitors | 191 |
CAR‐T therapy | Chimera antigen receptor (CAR) T cell therapy changes the synthesis of platelet‐activating factors (PAFs) | Targeting PAF remodeling | 170 |
Targeting immune checkpoint HLA‐E:CD94‐NKG2A | Immune checkpoint HLA‐E:CD94‐NKG2A on the tumor cells and T cell | Inhibiting the immune checkpoint | 69 |
R848‐loaded nanoparticle | Coated with platelet membrane, which contained resiquimod (R848) and the drug | Agonist of toll‐like receptor | 192 |
Nanoparticle with apatiniband and VDAs | Platelet membrane‐based nanoparticles loaded with apatinib, an antiangiogenic drug | Damage vessels and disrupt tumor angiogenesis | 193 |
Glucose oxidase (GOx)‐based starvation therapy | Application of platelet membrane | Improve the efficacy of killing tumors | 194 |
Mesoporous Fe single‐atom nanozyme (Fe‐SAzyme) coated with platelets | Platelet membrane used to camouflage single‐atom nanozyme | Destroy mitochondria | 196 |
β‐Mangostin‐loaded nanoparticles | The hybrid membrane of both platelets and tumor cells used to coat the β‐mangostin‐loaded nanoparticles | Improved ability targeting glioma | 197 |
Platelet exosomes | Produced by exosomes | FG@PEL to exert its cascade targeting effect against tumor | 198 |
Platelet vesicles with RSL‐3 | Platelet vesicles used to coat RSL‐3 | Pass through the stroma and disrupt tumor angiogenesis | 199 |
A nanoparticle coated with PSN peptide | Nanoparticles coated with a P‐selectin‐targeting peptide | Inhibiting platelet−tumor interaction and inflammation | 200 |
Quercetin (QCT)‐loaded platelet | Drug to be loaded into the cytoplasm of platelets | Target the glioblastoma tumor | 201 |
AuNR‐loaded platelets | Platelets loaded using AuNR | Target tumor cells precisely | 202 |
Abbreviations: CART, chimera antigen receptor T cell therapy; FAK, focal adhesion kinase; Fe‐SAzyme, Fe single‐atom nanozyme; GOx, glucose oxidase; MMP‐2, matrix metalloprotein‐2; PDGFR, platelet‐derived growth factor; PTAFR, platelet‐activating factor receptor.