N-Benzyl Indole-Benzoxazole Hybrids as Multi-Target Anticancer Agents Modulating mTOR, Apoptosis, and Lipid Dynamics in Breast Cancer

Objectives: Indole-benzoxazole hybrids are structurally versatile scaffolds with significant promise in anticancer drug development. This study aimed to synthesize N-benzyl-substituted indole-benzoxazole derivatives (IBB1-5) and to evaluate their antiproliferative potential and mechanistic effects in human breast cancer models. Materials and Methods: IBB1-5 were synthesized and screened for cytotoxic activity against MDA-MB-231 and MCF-7 cells using MTT assays. The most active compound, IBB-4, was further investigated in MDA-MB-231 cells through clonogenic assays and morphological analysis. Immunofluorescence staining was performed to assess mTOR, LC3, caspase-3, and β-tubulin expression and distribution. Lipid droplet dynamics were evaluated using Oil Red O and Nile Red staining, combined with three-dimensional surface-plot analysis. Results: values of 12.2 μM (MDA-MB-231) and 12.8 μM (MCF-7). Clonogenic assays revealed significant dose-dependent suppression of long-term proliferative capacity. Morphological alterations included cytoplasmic vacuolization and structural disorganization. Immunofluorescence analyses showed a marked downregulation of mTOR and a spatial redistribution of LC3, without significant changes in total fluorescence intensity. Increased caspase-3 immunoreactivity and pronounced disruption of β-tubulin indicated activation of apoptotic pathways and cytoskeletal destabilization. Lipid staining, supported by three-dimensional surface analysis, demonstrated prominent clustering and redistribution of intracellular lipid droplets. Conclusion: IBB-4 exerts multi-layered anticancer effects through coordinated modulation of proliferative signaling, apoptotic activation, cytoskeletal integrity, and lipid compartmentalization. These findings identify IBB-4 as a promising lead candidate for further molecular and preclinical investigations, particularly in triple-negative breast cancer.

Authors

Institutions

Publication Details

Journal
Turkish Journal of Pharmaceutical Sciences
Published
2026-11-06
DOI
https://doi.org/10.4274/tjps.galenos.2026.47564
Primary Topic
Heterocyclic Compound Synthesis and Bioactivity
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
NOV
article

N-Benzyl Indole-Benzoxazole Hybrids as Multi-Target Anticancer Agents Modulating mTOR, Apoptosis, and Lipid Dynamics in Breast Cancer

Burak Kuzu, Eda Açıkgöz, Mustafa Çakır
4 links
Turkish Journal of Pharmaceutical Sciences
Heterocyclic Compound Synthesis and Bioactivity
article

N-Benzyl Indole-Benzoxazole Hybrids as Multi-Target Anticancer Agents Modulating mTOR, Apoptosis, and Lipid Dynamics in Breast Cancer

Burak Kuzu, Eda Açıkgöz, Mustafa Çakır
article en

Abstract

Objectives: Indole-benzoxazole hybrids are structurally versatile scaffolds with significant promise in anticancer drug development. This study aimed to synthesize N-benzyl-substituted indole-benzoxazole derivatives (IBB1-5) and to evaluate their antiproliferative potential and mechanistic effects in human breast cancer models. Materials and Methods: IBB1-5 were synthesized and screened for cytotoxic activity against MDA-MB-231 and MCF-7 cells using MTT assays. The most active compound, IBB-4, was further investigated in MDA-MB-231 cells through clonogenic assays and morphological analysis. Immunofluorescence staining was performed to assess mTOR, LC3, caspase-3, and β-tubulin expression and distribution. Lipid droplet dynamics were evaluated using Oil Red O and Nile Red staining, combined with three-dimensional surface-plot analysis. Results: values of 12.2 μM (MDA-MB-231) and 12.8 μM (MCF-7). Clonogenic assays revealed significant dose-dependent suppression of long-term proliferative capacity. Morphological alterations included cytoplasmic vacuolization and structural disorganization. Immunofluorescence analyses showed a marked downregulation of mTOR and a spatial redistribution of LC3, without significant changes in total fluorescence intensity. Increased caspase-3 immunoreactivity and pronounced disruption of β-tubulin indicated activation of apoptotic pathways and cytoskeletal destabilization. Lipid staining, supported by three-dimensional surface analysis, demonstrated prominent clustering and redistribution of intracellular lipid droplets. Conclusion: IBB-4 exerts multi-layered anticancer effects through coordinated modulation of proliferative signaling, apoptotic activation, cytoskeletal integrity, and lipid compartmentalization. These findings identify IBB-4 as a promising lead candidate for further molecular and preclinical investigations, particularly in triple-negative breast cancer.

Turkish Journal of Pharmaceutical Sciences
Van Yüzüncü Yıl Üniversitesi (TR)
Good health and well-being
Openalex Percentile: Top 27%
Heterocyclic Compound Synthesis and Bioactivity
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.

Laika access coming soon