1Univ. of Maryland, College Park (United States) 2Ctr. for Cancer Research, National Cancer Institute, National Institutes of Health (United States) 3National Institutes of Health (United States) 4Marlene and Stewart Greenebaum Cancer Ctr., Univ. of Maryland School of Medicine (United States)
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Rationally designed bioconjugates of photosensitizers have been shown to enhance the photochemical effect of photodynamic therapy (PDT) via altering the sub-cellular localization of the photosensitizers or modulating the function of ATP-binding cassette (ABC) transporters. P-glycoprotein (ABCB1) and breast cancer resistance protein (ABCG2) are the two key members that contribute to chemoresistance and PDT resistance in cancer. Here, we introduce a porphyrin-based phospholipid conjugation strategy to circumvent and inhibit the efflux function of ABC drug transporters. Our results show the porphyrin-phospholipid conjugate enhances the photosensitizer accumulation and modulates the enzymatic activity and protein integrity of ABCB1 and ABCG2.
Barry J. Liang,Suresh V. Ambudkar, andHuang-Chiao Huang
"The use of bioconjugates of porphyrin to overcome ABC drug transporter-mediated drug resistance", Proc. SPIE PC11940, Optical Methods for Tumor Treatment and Detection: Mechanisms and Techniques in Photodynamic and Photobiomodulation Therapy XXX, (7 March 2022); https://doi.org/10.1117/12.2609732
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Barry J. Liang, Suresh V. Ambudkar, Huang-Chiao Huang, "The use of bioconjugates of porphyrin to overcome ABC drug transporter-mediated drug resistance," Proc. SPIE PC11940, Optical Methods for Tumor Treatment and Detection: Mechanisms and Techniques in Photodynamic and Photobiomodulation Therapy XXX, (7 March 2022); https://doi.org/10.1117/12.2609732