Buletinul Institutului Politehnic din Iași Secția Chimie și Inginerie Chimică ISSN: 2537-2947
ISSN-L: 0254-7104
2024, Volume 70(74), Issue 1 (January), pp. 81 - 88
Exploring Hesperidin's Therapeutic Potential in Cancer Therapy: A Review
MĂLINA MARIA CERNĂTESCU, “Grigore T. Popa” University of Medicine and
Pharmacy Iași, Faculty of Medicine, Iași, Romania, malinacernatescu1@gmail.com CLAUDIA COBZARU, “Gheorghe Asachi” Technical University of Iași,
“Cristofor Simionescu” Faculty of Chemical Engineering and Environmental
Protection, Iași, Romania CORINA CERNĂTESCU, “Gheorghe Asachi” Technical
University of Iași, “Cristofor Simionescu” Faculty of Chemical Engineering
and Environmental Protection, Iași, Romania
Abstract Hesperidin, a flavonoid abundant in citrus fruits, has
gathered attention for its promising anti-cancer properties. This review
explores the complex mechanisms through which hesperidin influences
oncogenesis and tumour progression. Studies reveal hesperidin's ability to
target key pathways involved in cancer development, including
hypoxia-induced HIF-1α activation, oxidative stress-mediated signalling, and
epithelial-mesenchymal transition (EMT). In vitro and in vivo experiments
showed hesperidin's capacity to inhibit angiogenesis, to suppress cell
proliferation, and to induce apoptosis in various cancer models.
Furthermore, hesperidin has been demonstrated to exhibit synergistic effects
with conventional chemotherapy, thereby enhancing its anti-cancer efficacy,
while simultaneously reducing its associated risks. Aside from the promising
preclinical findings, further clinical studies are needed in order to
elucidate hesperidin's therapeutic potential and to optimize its use in
cancer treatment strategies. Understanding the complex interaction between
hesperidin and cancer-related pathways could accelerate the development of
novel therapeutic approaches, with the goal of preventing cancer progression
and improving patient outcomes. Keywords: Hesperidin, Cancer therapy,
Hypoxia, Oxidative stress, Epithelial-mesenchymal transition.