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Topics {✒️}

fak-pi3k-akt-girdin signaling pathway release exosomal mir-23a-3p nf-κb/il-6/stat3 axis anti-pd-l1 antibody mpdl3280a tgf-β/smad signaling pathway 131i-anti-endoglin monoclonal antibody mir-199a-modified exosomes p53-dependent signaling pathway massoud vosough anti-vegf/vegfr therapy month download article/chapter pfkfb3-pd-l1 axis immune cell-derived exosomes increased α-fetoprotein concentrations pd-l1 significantly associates hbv-related hepatocellular carcinoma exosomal pd-l1 contributes small-cell lung cancer nonconventional antigen-presenting cells intra-tumoral expression levels pd-1 antibody increase immune-checkpoint inhibitors immune checkpoint inhibitors tumor-related exosomes contribute cancer-related death worldwide targeted alpha therapy hepatocellular carcinoma-derived exosomes advanced/metastatic hepatocellular carcinoma anti-cancer target targeted cancer therapy exposure-induced side effects molecular research center essential exosome components tgf-β signaling anti-angiogenic therapy anti-endoglin antibody immune checkpoint blockade epithelial–mesenchymal-transition epithelial-mesenchymal transition robo1-targeted radioimmunotherapy commonly accessible antigens exosome mir-335 cytotoxic t-lymphocyte tumor-specific monoclonal antibodies el-khoueiry ab regulatory immune cells dendritic cells pulsed anti-pd-1 response small molecule-based approaches differentiation antigens cd105

Questions {❓}

• Elsharkasy OM, Nordin JZ, Hagey DW, de Jong OG, Schiffelers RM, Andaloussi SE et al (2020) Extracellular vesicles as drug delivery systems: why and how?
• Lee HW, Cho KJ, Park JY (2020) Current status and future direction of immunotherapy in hepatocellular carcinoma: what do the data suggest?
• Mehlen P, Delloye-Bourgeois C, Chédotal A (2011) Novel roles for Slits and netrins: axon guidance cues as anticancer targets?
• Sahlin M, Bauden MP, Andersson R, Ansari DJTB (2015) Radioimmunotherapy—a potential novel tool for pancreatic cancer therapy?

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         headline:Novel antigens for targeted radioimmunotherapy in hepatocellular carcinoma
         description:Liver cancer is the sixth common cancer and forth cause of cancer-related death worldwide. Based on usually advanced stages of hepatocellular carcinoma (HCC) at the time of diagnosis, therapeutic options are limited and, in many cases, not effective, and typically result in the tumor recurrence with a poor prognosis. Radioimmunotherapy (RIT) offers a selective internal radiation therapy approach using beta or alpha emitting radionuclides conjugated with tumor-specific monoclonal antibodies (mAbs), or specific selective peptides. When compared to chemotherapy or radiotherapy, radiolabeled mAbs against cancer-associated antigens could provide a high therapeutic and exclusive radiation dose for cancerous cells while decreasing the exposure-induced side effects to healthy tissues. The recent advances in cancer immunotherapy, such as blockade of immune-checkpoint inhibitors (ICIs), has changed the landscape of cancer therapy, and the efficacy of different classes of immunotherapy has been tested in many clinical trials. Taking into account the use of ICIs in the liver tumor microenvironment, combined therapies with different approaches may enhance the outcome in the future clinical studies. With the development of novel immunotherapy treatment options in the recent years, there has been a great deal of information about combining the diverse treatment modalities to boost the effectiveness of immunomodulatory drugs. In this opinion review, we will discuss the recent advancements in RIT. The current status of immunotherapy and internal radiotherapy will be updated, and we will propose novel approaches for the combination of both techniques. Potential target antigens for radioimmunotherapy in Hepatocellular carcinoma (HCC). HCC radioimmunotherapy target antigens are the most specific and commonly accessible antigens on the surface of HCC cells. CTLA-4 ligand and receptor, TAMs, PD-1/PD-L, TIM-3, specific IEXs/TEXs, ROBO1, and cluster of differentiation antigens CD105, CD147 could all be used in HCC radioimmunotherapy. Abbreviations: TAMs, tumor-associated macrophages; CTLA-4, cytotoxic T-lymphocyte associated antigen-4; PD-1, Programmed cell death protein 1; PD-L, programmed death-ligand1; TIM-3, T-cell immunoglobulin (Ig) and mucin-domain containing protein-3; IEXs, immune cell-derived exosomes; TEXs, tumor-derived exosomes.
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            Immune checkpoint inhibitor
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      description:Liver cancer is the sixth common cancer and forth cause of cancer-related death worldwide. Based on usually advanced stages of hepatocellular carcinoma (HCC) at the time of diagnosis, therapeutic options are limited and, in many cases, not effective, and typically result in the tumor recurrence with a poor prognosis. Radioimmunotherapy (RIT) offers a selective internal radiation therapy approach using beta or alpha emitting radionuclides conjugated with tumor-specific monoclonal antibodies (mAbs), or specific selective peptides. When compared to chemotherapy or radiotherapy, radiolabeled mAbs against cancer-associated antigens could provide a high therapeutic and exclusive radiation dose for cancerous cells while decreasing the exposure-induced side effects to healthy tissues. The recent advances in cancer immunotherapy, such as blockade of immune-checkpoint inhibitors (ICIs), has changed the landscape of cancer therapy, and the efficacy of different classes of immunotherapy has been tested in many clinical trials. Taking into account the use of ICIs in the liver tumor microenvironment, combined therapies with different approaches may enhance the outcome in the future clinical studies. With the development of novel immunotherapy treatment options in the recent years, there has been a great deal of information about combining the diverse treatment modalities to boost the effectiveness of immunomodulatory drugs. In this opinion review, we will discuss the recent advancements in RIT. The current status of immunotherapy and internal radiotherapy will be updated, and we will propose novel approaches for the combination of both techniques. Potential target antigens for radioimmunotherapy in Hepatocellular carcinoma (HCC). HCC radioimmunotherapy target antigens are the most specific and commonly accessible antigens on the surface of HCC cells. CTLA-4 ligand and receptor, TAMs, PD-1/PD-L, TIM-3, specific IEXs/TEXs, ROBO1, and cluster of differentiation antigens CD105, CD147 could all be used in HCC radioimmunotherapy. Abbreviations: TAMs, tumor-associated macrophages; CTLA-4, cytotoxic T-lymphocyte associated antigen-4; PD-1, Programmed cell death protein 1; PD-L, programmed death-ligand1; TIM-3, T-cell immunoglobulin (Ig) and mucin-domain containing protein-3; IEXs, immune cell-derived exosomes; TEXs, tumor-derived exosomes.
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         Hepatocellular carcinoma
         Immune checkpoint inhibitor
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         Medical Biochemistry
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            name:ACECR
            address:
               name:Department of Regenerative Medicine, Cell Science Research Center, Royan Institute for Stem Cell Biology and Technology, ACECR, Tehran, Iran
               type:PostalAddress
            type:Organization
            name:Karolinska Institute
            address:
               name:Experimental Cancer Medicine, Institution for Laboratory Medicine, Karolinska Institute, Stockholm, Sweden
               type:PostalAddress
            type:Organization
      email:[email protected]
PostalAddress:
      name:Department of Regenerative Medicine, Cell Science Research Center, Royan Institute for Stem Cell Biology and Technology, ACECR, Tehran, Iran
      name:Departments of Pathology and Medicine, UC San Diego, La Jolla, USA
      name:Department of Regenerative Medicine, Cell Science Research Center, Royan Institute for Stem Cell Biology and Technology, ACECR, Tehran, Iran
      name:Research Center for Biochemistry and Nutrition in Metabolic Diseases, Institute for Basic Sciences, Kashan University of Medical Sciences, Kashan, Iran
      name:Cellular and Molecular Research Center, Research Institute for Prevention of Non-Communicable Diseases, Qazvin University of Medical Sciences, Qazvin, Iran
      name:Departments of Pathology and Medicine, UC San Diego, La Jolla, USA
      name:World-Class Research Center “Digital Biodesign and Personalized Healthcare”, Sechenov First Moscow State Medical University, Moscow, Russia
      name:Institute for Regenerative Medicine, Sechenov First Moscow State Medical University, Moscow, Russia
      name:Chemistry Department, Lomonosov Moscow State University, Moscow, Russia
      name:School of Biomedical Engineering, University of Technology Sydney, Sydney, Australia
      name:World-Class Research Center “Digital Biodesign and Personalized Healthcare”, Sechenov First Moscow State Medical University, Moscow, Russia
      name:Institute for Regenerative Medicine, Sechenov First Moscow State Medical University, Moscow, Russia
      name:Chemistry Department, Lomonosov Moscow State University, Moscow, Russia
      name:Experimental Cancer Medicine, Institution for Laboratory Medicine, Karolinska Institute, Stockholm, Sweden
      name:Department of Regenerative Medicine, Cell Science Research Center, Royan Institute for Stem Cell Biology and Technology, ACECR, Tehran, Iran
      name:Experimental Cancer Medicine, Institution for Laboratory Medicine, Karolinska Institute, Stockholm, Sweden
WebPageElement:
      isAccessibleForFree:
      cssSelector:.main-content

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