Reduced Polydopamine Coated Graphene for Delivery of Hset1 Antisense As a Photothermal and Gene Therapy of Breast Cancer Publisher



Babavalian A¹ ; Tekie FSM^{1, 2} ; Ayazi H³ ; Ranjbar S¹ ; Varshochian R^{1, 4} ; Radmalelkshahi M⁵ ; Akhavan O³ ; Dinarvand R^{1, 2, 6} Show Affiliations
Source: Journal of Drug Delivery Science and Technology Published:2022

Abstract

Breast cancer is the most prevalent type of cancer in women; hence, many researches have been focused on developing effective treatment protocols. In this study, a novel nanocarrier was fabricated for gene and photothermal combination cancer therapy by conjugating histone methyltransferase complex subunit SET1 (hSET1) on reduced polydopamine coated graphene oxide nanosheets (rGO-PDA). The rGO-PDA nanocarriers provide higher near-infrared absorption and further integrating with hSET1 antisense as an anticancer gene that down-regulates the amount of hSET1 overexpressed and suppresses the proliferation of cancer cells. The nanoplatform was prepared by polymerizing of dopamine, a mussel adhesive protein, on graphene oxide nanosheets in alkaline media, followed by conjugation of hSET1 antisense on rGO-PDA nanocarriers which was examined by gel retardation assay. After Laser irradiation, the amount of hSET1 was estimated in overexpressed cells treated with this formulation by real-time reverse transcription-polymerase chain reaction (RT-PCR). The size and zeta potential of prepared nanocarriers were 140 nm and −29.4 mv respectively. In vitro cellular tests confirmed that the prepared nanoplatform was biocompatible with no cell toxicity. The nanocarrier as a photothermal agent generating hyperthermia, led to a better release of hSET1 antisense under NIR (near-infrared) and more apoptosis of cancer cells and RT-PCR implied a considerable decrease of hSET1 expression. Outstanding photothermal conversion and suitable potential of rGO-PDA for interaction with oligonucleotides is expected as a suitable system for gene delivery and photoresponsive therapy of solid tumors simultaneously. © 2022 Elsevier B.V.