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Kamal et al. J Cancer Metastasis Treat 2019;5:11  I  http://dx.doi.org/10.20517/2394-4722.2018.89                           Page 7 of 14

               indications including acute relapses of multiple sclerosis, optic neuritis, neuromyelitis optica and uveitis.
                                                                       [77]
               2B3-201 has completed a Phase I clinical trial in healthy volunteers .

               2-BBB is a clear example of industry-driven research aiming at developing innovative passive targeting
               technologies to brain and brain metastases. They use triple passive targeting techniques to offer optimal
               safety and efficacy profiles, Glutathione passively targeting the cancerous intracellular reductive
                                                                     [77]
               environment, PEGylation and liposomal vesicular carrier system .
               Nucleic acid
               RNA interference (RNAi) is an endogenous pathway for post-transcriptional silencing of gene expression
               that is triggered by double-stranded RNA, including endogenous microRNA (miRNA) and synthetic short
                             [79]
                                                                             [80]
                                                                                          [81]
               interfering RNA . MicroRNA-122 mediated RNAi brings new prospects . Zhang et al.  miRNA-1258 in
               BMBC cells inhibited heparanase which regulates many molecules involved in angiogenesis and metastasis
               of the tumor.
               Advanced physically manipulated systems to disrupt BBB
               Another modality of addressing BBB passively is advanced physically manipulated systems that can be
               tightly mediated by stimuli to treat diseases specifically and with a controlled dosage of drugs. Physical
               manipulation can be achieved based on ultrasound, electricity, magnetism and photonic emission
                          [82]
                                          [83]
               technologies . Davalos et al.  applied pulsed electric fields into brain tissue of an animal, to cause
               temporary disruption of the BBB in a volume of brain tissue near the source of the pulsed electric fields over
               a specified time interval.

               The use of focused ultrasound (FUS) combined with circulating microbubbles is a non-invasive method
               that increases the permeability of BBTB and improves outcomes of trastuzumab; this technique was used by
                        [84]
               Park et al.  to improve outcomes with trastuzumab in a breast cancer brain metastasis model. Similarly,
               FUS in combination with microbubbles was able to temporarily disrupt the BBB enhancing the anti-tumor
                                                                  [85]
               efficacy of the two anti-HER2 agents combination therapy . Moreover, reversible disruption of the BBB
               by bursts of low frequency MRI-guided ultrasound enhances the brain delivery of monoclonal antibody -
               Herceptin (trastuzumab) in mice [86,87] .

               Active targeting
                                                                    [47]
               Active targeting was proposed for improved targeting efficacy . These strategies consist in incorporating
               affinity molecules or taking advantage of influx transport systems expressed within the BBB/BBTB
               depending on specific interactions of ligand-receptor and antibody-antigen [47,88,89] . Also, several ligands have
               been studied and utilized to shuttle nanoparticles, antibodies, and drugs across the BBB and into the brain
                   [90]
               cells  [Figure 1]. Supplementary Table 2 summarizes recent studies of actively targeted treatments for
               BCBM.

               Receptor-mediated transcytosis/ligand-based
               An overexpression of receptors or antigens in cancer acts as a potential target to achieve efficient drug
                                                   [47]
               uptake via receptor-mediated endocytosis . Moreover, receptor-mediated transcytosis (RMT) allows for
               BBB transport of various macromolecules after initial binding of a targeting ligand to a receptor expressed
                                        [91]
               on the brain endothelial cells . Tumor-targeting ligands such as peptides and antibodies may effectively
               aid certain cytotoxic agents (either biological or synthetic) to deliver to the tumor cells, thereby improving
                                                                                          [92]
               therapeutic efficacy while limiting the exposure of normal tissues to the cytotoxic agents . The transferrin
               receptor, the low-density lipoprotein receptor-related protein 1 (LRP-1), the insulin receptor and the
               nicotinic acetylcholine receptors are examples of receptor expression on the BBB.
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