Nagy Ferenc István, Adamecz Dóra Izabella, Baji Ádám, Kiricsi Ágnes, Huliák Ildikó, Rónavári Andrea, Kónya Zoltán, Frank Éva, Gopisetty Mohana Krishna, Kiricsi Mónika
Department of Biochemistry and Molecular Biology, Doctoral School of Biology, University of Szeged, Közép Fasor 52, H-6726 Szeged, Hungary.
Department of Organic Chemistry, University of Szeged, Dóm tér 8, H-6720 Szeged, Hungary.
Pharmaceutics. 2023 Feb 9;15(2):584. doi: 10.3390/pharmaceutics15020584.
Multidrug resistance (MDR) is a serious hurdle to successful cancer therapy. Here, we examined the efficiency of novel semi-synthetic dihydrotestosterone derivatives, more specifically androstano-arylpyrimidines in inhibiting the efflux activity of ATP-binding cassette (ABC) transporters and sensitizing inherently MDR colon cancer cells to various chemotherapy drugs. Using the Rhodamine123 accumulation assay, we evaluated the efflux activity of cancer cells following treatments with androstano-arylpyrimidines. We found that acetylated compounds were capable of attenuating the membrane efflux of inherently MDR cells; however, deacetylated counterparts were ineffective. To delineate the possible molecular mechanisms underlying these unique activities of androstano-arylpyrimidines, the degree of apoptosis induction was assessed by AnnexinV-based assays, both upon the individual as well as by steroid and chemotherapy agent combination treatments. Five dihydrotestosterone derivatives applied in combination with Doxorubicin or Epirubicin triggered massive apoptosis in MDR cells, and these combinations were more efficient than chemotherapy drugs together with Verapamil. Furthermore, our results revealed that androstano-arylpyrimidines induced significant endoplasmic reticulum stress (ER stress) but did not notably modulate ABC transporter expression. Therefore, ER stress triggered by acetylated androstano-arylpyrimidines is probably involved in the mechanism of efflux pump inhibition and drug sensitization which can be targeted in future drug developments to defeat inherently multidrug-resistant cancer.
多药耐药性(MDR)是癌症治疗成功的严重障碍。在此,我们研究了新型半合成二氢睾酮衍生物,更具体地说是雄甾烷芳基嘧啶抑制ATP结合盒(ABC)转运蛋白外排活性以及使固有多药耐药性结肠癌细胞对各种化疗药物敏感的效率。使用罗丹明123积累试验,我们评估了用雄甾烷芳基嘧啶处理后癌细胞的外排活性。我们发现乙酰化化合物能够减弱固有多药耐药细胞的膜外排;然而,去乙酰化的对应物则无效。为了阐明雄甾烷芳基嘧啶这些独特活性背后可能的分子机制,通过基于膜联蛋白V的试验评估了单独处理以及类固醇与化疗药物联合处理时的凋亡诱导程度。五种二氢睾酮衍生物与阿霉素或表柔比星联合应用可在多药耐药细胞中引发大量凋亡,并且这些联合用药比化疗药物与维拉帕米联合更有效。此外,我们的结果表明雄甾烷芳基嘧啶诱导了显著的内质网应激(ER应激),但并未显著调节ABC转运蛋白的表达。因此,乙酰化雄甾烷芳基嘧啶引发的ER应激可能参与了外排泵抑制和药物致敏机制,这在未来的药物开发中可作为靶点来攻克固有多药耐药性癌症。