Anti-Breast Cancer Properties and In Vivo Safety Profile of a Bis-Carbazole Derivative

<b>Background:</b> Carbazoles represent one of the most important classes of nitrogen-based tricyclic aromatic heterocycles and are present in natural sources and chemically obtained drugs. Recently, several research groups disclosed their large biological and chemical applications in different fields, leading to an increased interest towards this class of molecules. Some of the obtained derivatives have been successfully employed in the clinical treatment of different tumor types, but the onset of heavy side effects impaired their efficacy and discouraged their use. Pursuing the aim of obtaining carbazoles with less negative features, a lot of chemically modified compounds have been produced and evaluated. <b>Objectives/Methods</b>: In this paper, we describe the in vitro and in vivo evaluation of a bis-carbazole derivative with strong anticancer properties against two breast cancer cell lines. <b>Results</b>: This compound has been found to impact the cell cytoskeleton dynamics, triggering the activation of some key proteins playing a role in the intrinsic and extrinsic apoptotic pathways. Equally important, this derivative has been found to be selective for cancer cells and has shown a safe profile in Balb/c-treated mice. <b>Conclusions</b>: Overall, the disclosed outcomes represent an important landmark for encouraging further studies directed toward the potentiation of this lead to be potentially exploited in both preclinical and clinical applications.

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Publication Details

Journal
Pharmaceutics
Published
2025-03-25
DOI
https://doi.org/10.3390/pharmaceutics17040415
Primary Topic
Synthesis and biological activity
Type
article
Field-Weighted Citation Impact
0.00

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article

Anti-Breast Cancer Properties and In Vivo Safety Profile of a Bis-Carbazole Derivative

Camillo Rosano, Christophe Rochais, Annaluisa Mariconda, Patrick Dallemagne et al.
Pharmaceutics
Synthesis and biological activity
article

Anti-Breast Cancer Properties and In Vivo Safety Profile of a Bis-Carbazole Derivative

Camillo Rosano, Christophe Rochais, Annaluisa Mariconda, Patrick Dallemagne, Maria Stefania Sinicropi, Domenico Iacopetta, Imène Ben Toumia, Pasquale Longo, Jessica Ceramella, Leila Chekir Ghédira, Mouna Maâtouk
article en

Abstract

<b>Background:</b> Carbazoles represent one of the most important classes of nitrogen-based tricyclic aromatic heterocycles and are present in natural sources and chemically obtained drugs. Recently, several research groups disclosed their large biological and chemical applications in different fields, leading to an increased interest towards this class of molecules. Some of the obtained derivatives have been successfully employed in the clinical treatment of different tumor types, but the onset of heavy side effects impaired their efficacy and discouraged their use. Pursuing the aim of obtaining carbazoles with less negative features, a lot of chemically modified compounds have been produced and evaluated. <b>Objectives/Methods</b>: In this paper, we describe the in vitro and in vivo evaluation of a bis-carbazole derivative with strong anticancer properties against two breast cancer cell lines. <b>Results</b>: This compound has been found to impact the cell cytoskeleton dynamics, triggering the activation of some key proteins playing a role in the intrinsic and extrinsic apoptotic pathways. Equally important, this derivative has been found to be selective for cancer cells and has shown a safe profile in Balb/c-treated mice. <b>Conclusions</b>: Overall, the disclosed outcomes represent an important landmark for encouraging further studies directed toward the potentiation of this lead to be potentially exploited in both preclinical and clinical applications.

PharmaceuticsVol. 17(4)
University of Salerno (IT), University of Monastir (TN), University of Basilicata (IT), Normandie Université (FR), Ospedale Policlinico San Martino (IT), University of Calabria (IT)
Ministero della Salute
Good health and well-being
Openalex Percentile: Top 96%
Synthesis and biological activity
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