TY - JOUR
T1 - Integrated systems biology and structural approaches to discover novel biomarkers and small molecule inhibitors using the gene expression data from drug-resistant breast cancer cell lines
AU - Alghamdi, Suad A.
AU - Alissa, Mohammed
AU - Suleman, Muhammad
N1 - Publisher Copyright:
© 2025 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group.
PY - 2025/12/31
Y1 - 2025/12/31
N2 - Breast cancer, the leading cause of cancer-related deaths in women, is driven by multidrug resistance, highlighting the urgent need for novel therapeutic targets. Consequently, we employed network-based gene expression profiling to analyse datasets from normal and tamoxifen-resistant MCF7 cell lines. The analysis identified 372 DEGs, including 133 upregulated and 239 downregulated genes, with ISG15 emerging as the top hub gene. Survival analyses indicated that high ISG15 expression correlates with poorer overall survival in breast cancer. To identify potent inhibitors of ISG15, we screened an anticancer drug database and selected three top hits with docking scores of −6.6, −6.5 and −5.4 kcal/mol. Molecular dynamics simulations confirmed the dynamic stability and strong binding affinity of these top hits. The top hit (1-3) complexes showed favourable binding-free energies of −31.57, −23.92 and −28.05 kcal/mol, respectively, with desirable pharmacokinetic properties. This study highlights promising drug candidates targeting ISG15 in tamoxifen-resistant breast cancer, warranting further experimental validation.
AB - Breast cancer, the leading cause of cancer-related deaths in women, is driven by multidrug resistance, highlighting the urgent need for novel therapeutic targets. Consequently, we employed network-based gene expression profiling to analyse datasets from normal and tamoxifen-resistant MCF7 cell lines. The analysis identified 372 DEGs, including 133 upregulated and 239 downregulated genes, with ISG15 emerging as the top hub gene. Survival analyses indicated that high ISG15 expression correlates with poorer overall survival in breast cancer. To identify potent inhibitors of ISG15, we screened an anticancer drug database and selected three top hits with docking scores of −6.6, −6.5 and −5.4 kcal/mol. Molecular dynamics simulations confirmed the dynamic stability and strong binding affinity of these top hits. The top hit (1-3) complexes showed favourable binding-free energies of −31.57, −23.92 and −28.05 kcal/mol, respectively, with desirable pharmacokinetic properties. This study highlights promising drug candidates targeting ISG15 in tamoxifen-resistant breast cancer, warranting further experimental validation.
KW - Breast cancer
KW - ISG15
KW - Molecular docking
KW - Molecular dynamics simulations
KW - System biology
KW - drug resistance
UR - https://www.scopus.com/pages/publications/105012611272
U2 - 10.1080/16583655.2025.2541441
DO - 10.1080/16583655.2025.2541441
M3 - Article
AN - SCOPUS:105012611272
SN - 1658-3655
VL - 19
JO - Journal of Taibah University for Science
JF - Journal of Taibah University for Science
IS - 1
M1 - 2541441
ER -