Rose Bengal–Amphiphilic Peptide Conjugate for Enhanced Photodynamic Therapy of Malignant Melanoma
Author(s) -
Simanpreet Kaur Dhillon,
Simon L. Porter,
Nermeen Rizk,
Yingjie Sheng,
Thomas McKaig,
Kathyrn Burnett,
B.C. White,
Heather Nesbitt,
Rubeta Matin,
A. P. McHale,
John F. Callan
Publication year - 2020
Publication title -
journal of medicinal chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.01
H-Index - 261
eISSN - 1520-4804
pISSN - 0022-2623
DOI - 10.1021/acs.jmedchem.9b01802
Subject(s) - photodynamic therapy , rose bengal , chemistry , melanoma , conjugate , oxidative stress , reactive oxygen species , cancer research , peptide , photosensitizer , skin cancer , cancer , pharmacology , medicine , biochemistry , photochemistry , mathematical analysis , mathematics , organic chemistry
Malignant melanoma is an aggressive skin cancer with poor survival outcomes for patients diagnosed at an advanced stage. While targeted serine/threonine-protein kinase B-Raf (BRAF) and immune checkpoint inhibitors have improved survival outcomes for a proportion of these patients, response rates remain variable. There is a need, therefore, for more effective treatments to bolster the options available for melanoma patients. In this manuscript, we covalently attached Rose Bengal (RB) to the amphipathic peptide (AMP) C(KLAKLAK) 2 and determined the effectiveness of the resulting RB-C(KLAKLAK) 2 conjugate as a photodynamic therapy (PDT) sensitizer. RB-C(KLAKLAK) 2 -mediated PDT treatment of subcutaneous B16-F10-Luc2 tumors in C57 mice resulted in lesions that were 479% smaller at the end of the study than animals treated with RB-mediated PDT. The synergistic effect between RB and C(KLAKLAK) 2 has been attributed to the AMP sensitizing cells to reactive oxygen species (ROS), making them more susceptible to ROS-induced oxidative stress.
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