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      Glypican-3: A New Target for Diagnosis and Treatment of Hepatocellular Carcinoma

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          Abstract

          Liver cancer is the second leading cause of cancer-related deaths worldwide, and hepatocellular carcinoma is the most common type. The pathogenesis of hepatocellular carcinoma is concealed, its progress is rapid, its prognosis is poor, and the mortality rate is high. Therefore, novel molecular targets for hepatocellular carcinoma early diagnosis and development of targeted therapy are critically needed. Glypican-3, a cell-surface glycoproteins in which heparan sulfate glycosaminoglycan chains are covalently linked to a protein core, is overexpressed in HCC tissues but not in the healthy adult liver. Thus, Glypican-3 is becoming a promising candidate for liver cancer diagnosis and immunotherapy. Up to now, Glypican-3 has been a reliable immunohistochemical marker for hepatocellular carcinoma diagnosis, and soluble Glypican-3 in serum has becoming a promising marker for liquid biopsy. Moreover, various immunotherapies targeting Glypican-3 have been developed, including Glypican-3 vaccines, anti- Glypican-3 immunotoxin and chimeric-antigen-receptor modified cells. In this review, we summarize and analyze the structure and physicochemical properties of Glypican-3 molecules, then review their biological functions and applications in clinical diagnosis, and explore the diagnosis and treatment strategies based on Glypican-3.

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          Wnt signalling and its impact on development and cancer.

          The Wnt signalling pathway is an ancient system that has been highly conserved during evolution. It has a crucial role in the embryonic development of all animal species, in the regeneration of tissues in adult organisms and in many other processes. Mutations or deregulated expression of components of the Wnt pathway can induce disease, most importantly cancer. The first gene to be identified that encodes a Wnt signalling component, Int1 (integration 1), was molecularly characterized from mouse tumour cells 25 years ago. In parallel, the homologous gene Wingless in Drosophila melanogaster, which produces developmental defects in embryos, was characterized. Since then, further components of the Wnt pathway have been identified and their epistatic relationships have been defined. This article is a Timeline of crucial discoveries about the components and functions of this essential pathway.
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            Heparan sulphate proteoglycans fine-tune mammalian physiology.

            Heparan sulphate proteoglycans reside on the plasma membrane of all animal cells studied so far and are a major component of extracellular matrices. Studies of model organisms and human diseases have demonstrated their importance in development and normal physiology. A recurrent theme is the electrostatic interaction of the heparan sulphate chains with protein ligands, which affects metabolism, transport, information transfer, support and regulation in all organ systems. The importance of these interactions is exemplified by phenotypic studies of mice and humans bearing mutations in the core proteins or the biosynthetic enzymes responsible for assembling the heparan sulphate chains.
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              Cancer Cell-Selective In Vivo Near Infrared Photoimmunotherapy Targeting Specific Membrane Molecules

              Three major modes of cancer therapies, surgery, radiation and chemotherapy, have been the mainstay of modern oncologic therapy. To minimize side effects, molecular targeted cancer therapies including armed antibody therapy have been developed with limited success. In this study, we developed a new type of molecular targeted cancer therapy, photoimmunotherapy (PIT), employing a target-specific photosensitizer based on a near infrared (NIR) phthalocyanine dye, IR700, conjugated to monoclonal antibodies (MAb) targeting epidermal growth factor receptors (EGFR). Cell death was induced immediately only upon irradiating, MAb-IR700 bound, target cells with NIR light. In vivo tumor shrinkage after irradiation with NIR light was observed only in target EGFR-expressing cells. The MAb-IR700 conjugates were most effective when bound to the cell membrane, producing no phototoxicity when not bound, suggesting a different mechanism for PIT compared with conventional photodynamic therapies. Target selective PIT enables treatment of cancer based on MAb binding on the cell membrane.
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                Author and article information

                Journal
                J Cancer
                J Cancer
                jca
                Journal of Cancer
                Ivyspring International Publisher (Sydney )
                1837-9664
                2020
                3 February 2020
                : 11
                : 8
                : 2008-2021
                Affiliations
                [1 ]National Key Laboratory of Medical Immunology &Institute of Immunology, Second Military Medical University, Shanghai, China
                [2 ]Institute of Organ Transplantation, Changzheng Hospital, Second Military Medical University, Shanghai, China
                [3 ]Department of Neurology, Changhai Hospital, Second Military Medical University, Shanghai, China
                [4 ]Department of Pathology ,Changhai Hospital, Second Military Medical University, Shanghai, China
                Author notes
                ✉ Corresponding authors: Yanfang Liu, Department of pathology, Changhai Hospital, Second Military Medical University, Shanghai, China; Tel: +86-21-31162262; Email: Liuyanfang00215@ 123456163.com and Jianming Zheng, Department of pathology, Changhai Hospital, Second Military Medical University, Shanghai, China; Shanghai, China; Tel: +86-21-31162257; Email: Jmzheng1962@ 123456smmu.edu.cn

                *Meng Guo and Hailing Zhang are co-first authors.

                Competing Interests: The authors have declared that no competing interest exists.

                Article
                jcav11p2008
                10.7150/jca.39972
                7052944
                32127929
                81c281cb-7a14-49d0-99dd-9b4a4f32dec2
                © The author(s)

                This is an open access article distributed under the terms of the Creative Commons Attribution License ( https://creativecommons.org/licenses/by/4.0/). See http://ivyspring.com/terms for full terms and conditions.

                History
                : 4 September 2019
                : 4 January 2020
                Categories
                Review

                Oncology & Radiotherapy
                hepatocellular carcinoma,glypican-3,immunotherapy,diagnostics
                Oncology & Radiotherapy
                hepatocellular carcinoma, glypican-3, immunotherapy, diagnostics

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