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      Phage Display Libraries: From Binders to Targeted Drug Delivery and Human Therapeutics

      Molecular Biotechnology
      Springer Science and Business Media LLC

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          Most cited references139

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          Somatic generation of antibody diversity.

          In the genome of a germ-line cell, the genetic information for an immunoglobulin polypeptide chain is contained in multiple gene segments scattered along a chromosome. During the development of bone marrow-derived lymphocytes, these gene segments are assembled by recombination which leads to the formation of a complete gene. In addition, mutations are somatically introduced at a high rate into the amino-terminal region. Both somatic recombination and mutation contribute greatly to an increase in the diversity of antibody synthesized by a single organism.
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            Continuous cultures of fused cells secreting antibody of predefined specificity.

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              VEGF as a Key Mediator of Angiogenesis in Cancer

              Vascular endothelial growth factor (VEGF) is a homodimeric glycoprotein with a molecular weight of approximately 45 kDa. It is the key mediator of angiogenesis (the formation of new blood vessels), and binds two VEGF receptors (VEGF receptor-1 and VEGF receptor-2), which are expressed on vascular endothelial cells. In healthy humans, VEGF promotes angiogenesis in embryonic development and is important in wound healing in adults. VEGF is the key mediator of angiogenesis in cancer, in which it is up-regulated by oncogene expression, a variety of growth factors and also hypoxia. Angiogenesis is essential for cancer development and growth: before a tumor can grow beyond 1–2 mm, it requires blood vessels for nutrients and oxygen. The production of VEGF and other growth factors by the tumor results in the ‘angiogenic switch’, where new vasculature is formed in and around the tumor, allowing it to grow exponentially. Tumor vasculature formed under the influence of VEGF is structurally and functionally abnormal. Blood vessels are irregularly shaped, tortuous, have dead ends and are not organized into venules, arterioles and capillaries. They are also leaky and hemorrhagic, which leads to high interstitial pressure. These characteristics mean that tumor blood flow is suboptimal, resulting in hypoxia and further VEGF production. This central role of VEGF in the production of tumor vasculature makes it a rational target for anticancer therapy.
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                Author and article information

                Journal
                Molecular Biotechnology
                Mol Biotechnol
                Springer Science and Business Media LLC
                1073-6085
                1559-0305
                April 2019
                February 7 2019
                April 2019
                : 61
                : 4
                : 286-303
                Article
                10.1007/s12033-019-00156-8
                30729435
                25cb00d1-7539-41ed-ad26-d0a67d32f1c0
                © 2019

                http://www.springer.com/tdm

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