"Long Term Anti-Corrosion Effect of Nitrogen-Doped Amorphous Carbon Film on Transparent and Deformable Ultrathin Copper Film"

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Small-sized Deformable Shear Sensor Array for Direct Monitoring of Shear Force and Shear Distribution

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Independently Responsive Stretchable Electroluminescent Platform for Electronic Skin under Multi-Stimulation

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Electro-Photoluminescence Color Change for Deformable Visual Signaling in Soft Robotics

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Assembling Conductive Particles on Stretchable Film for Anisotropic Interconnections

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Electronic Skin with Localized Piezo-resistive Material for Omni-directional Pressure Profiling

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Liposomes targeting the cancer cell-exposed receptor, claudin-4, for pancreatic cancer chemotherapy

Abstract Background Claudin-4 (CLDN4), a tight junction protein, is overexpressed in several types of cancer, and is considered a biomarker for cancer-targeted treatment. CLDN4 is not exposed in normal cells, but becomes accessible in cancer cells, in which tight junctions are weakened. Notably, surface-exposed CLDN4 has recently been found to act as a receptor for Clostridium perfringens enterotoxin (CPE) and fragment of CPE (CPE17) that binds to the second domain of CLDN4. Methods Here, we sought to develop a CPE17-containing liposome that targets pancreatic cancers through binding to exposed CLDN4. Results Doxorubicin (Dox)-loaded, CPE17-conjugated liposomes (D@C-LPs) preferentially targeted CLDN4-expressing cell lines, as evidenced by greater uptake and cytotoxicity compared with CLDN4-negative cell lines, whereas uptake and cytotoxicity of Dox-loaded liposomes lacking CPE17 (D@LPs) was similar for both CLDN4-positive and negative cell lines. Notably, D@C-LPs showed greater accumulation in targeted pancreatic tumor tissues compared with normal pancreas tissue; in contrast, Dox-loaded liposomes lacking CPE17 (D@LPs) showed little accumulation in pancreatic tumor tissues. Consistent with this, D@C-LPs showed greater anticancer efficacy compared with other liposome formulations and significantly extended survival. Conclusions We expect our findings will aid in the prevention and treatment of pancreatic cancer and provide a framework for identifying cancer-specific strategies that target exposed receptors. Graphical Abstrac