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The term "Tumor cell membrane fusion/lysis via viral replication" does not refer to a single molecular target or receptor. Instead, it describes a **therapeutic strategy** that exploits the ability of certain viruses—especially those engineered for oncolytic virotherapy—to infect tumor cells. These viruses use their **viral membrane fusion proteins** ("fusogens") to merge their envelope with the tumor cell's plasma membrane, allowing entry and subsequent replication within the cancer cell. This process can lead directly to **tumor cell lysis** through non-apoptotic mechanisms and may also promote immune recognition by exposing tumor antigens after lysis[4]. The actual molecular targets are diverse classes of **viral fusogenic glycoproteins**, which are essential for mediating this process across all enveloped viruses[1][2]. These proteins are major targets for antiviral drugs and vaccines but are not themselves human therapeutic targets like receptors or enzymes. In summary, "Tumor cell membrane fusion/lysis via viral replication" is an approach rather than a discrete molecule or receptor; its core components are various **viral fusogenic proteins**, which do not have a universal canonical name or abbreviation applicable across all contexts.
Inhibition of membrane fusion between virus and host cell Blockade of conformational changes in the viral envelope glycoprotein required for entry[1]
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