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      MDA-9/Syntenin (SDCBP): Novel gene and therapeutic target for cancer metastasis

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          EMT Transition States during Tumor Progression and Metastasis

          Epithelial-mesenchymal transition (EMT) is a process in which epithelial cells acquire mesenchymal features. In cancer, EMT is associated with tumor initiation, invasion, metastasis, and resistance to therapy. Recently, it has been demonstrated that EMT is not a binary process, but occurs through distinct cellular states. Here, we review the recent studies that demonstrate the existence of these different EMT states in cancer and the mechanisms regulating their functions. We discuss the different functional characteristics, such as proliferation, propagation, plasticity, invasion, and metastasis associated with the distinct EMT states. We summarize the role of the transcriptional and epigenetic landscapes, gene regulatory network and their surrounding niche in controlling the transition through the different EMT states.
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            Emerging Biological Principles of Metastasis.

            Metastases account for the great majority of cancer-associated deaths, yet this complex process remains the least understood aspect of cancer biology. As the body of research concerning metastasis continues to grow at a rapid rate, the biological programs that underlie the dissemination and metastatic outgrowth of cancer cells are beginning to come into view. In this review we summarize the cellular and molecular mechanisms involved in metastasis, with a focus on carcinomas where the most is known, and we highlight the general principles of metastasis that have begun to emerge.
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              Tumor angiogenesis: therapeutic implications.

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                Author and article information

                Journal
                Pharmacological Research
                Pharmacological Research
                Elsevier BV
                10436618
                May 2020
                May 2020
                : 155
                : 104695
                Article
                10.1016/j.phrs.2020.104695
                32061839
                5366ec03-a0bd-498d-bb97-e61c654e6819
                © 2020

                https://www.elsevier.com/tdm/userlicense/1.0/

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