TY - JOUR
T1 - An immunohistochemical study of Saussurea lappa nanoparticle on transformed cells in mice induced with benzo[a]pyrene for oral squamous cell carcinoma
AU - Budhy, Theresia Indah
AU - Arundina, Ira
AU - Irmawati, Anis
AU - Ming, Cheng Hwee
AU - Surboyo, Meircurius Dwi Condro
AU - Moelyanto, Azzahra Salsabila Adira
AU - Dewanata, Pandu
AU - Saqifa, Naqiya
N1 - Publisher Copyright:
© 2025 Elsevier GmbH.
PY - 2026/3
Y1 - 2026/3
N2 - Background Saussurea lappa , a plant used in traditional medicine, has shown promise in cancer treatment This study aimed to evaluate the therapeutic efficacy of Saussurea lappa nanoparticles using immunohistochemical analysis in a benzo[ a ]pyrene-induced mouse model of oral squamous cell carcinoma (OSCC). The investigation focused on the expression of markers related to apoptosis (Bax, Caspase-3, BCL-2), inflammation (TNF-α), proliferation (Ki-67), and tumor suppression (p53). Methods A true experimental design was employed using male Mus musculus mice. OSCC was induced via exposure to benzo[ a ]pyrene. Following induction, mice were treated perorally with Saussurea lappa nanoparticles at doses of 50, 100, and 200 mg/kg body weight, while the control group received CMC-Na. Buccal mucosa samples were collected for immunohistochemical analysis, assessing dose-dependent effects of Saussurea lappa nanoparticles on the expression of Bax, Caspase-3, BCL-2, TNF-α, Ki-67 and p53. Result Saussurea lappa nanoparticles demonstrated dose-dependent therapeutic effects in the OSCC mouse model. They significantly upregulated Bax, Caspase-3, TNF-α, and p53, while downregulating BCL-2 and Ki-67expression. The highest dose (200 mg/kg) showed the most pronounced effects, indicating enhanced apoptosis, reduced proliferation, and modulation of the inflammatory environment. Conclusion These findings suggest that Saussurea lappa nanoparticles, particularly at a dose of 200 mg/kg BW, effectively promote apoptosis, inhibit cell proliferation, and suppress anti-apoptotic pathways. This highlights their potential as a promising therapeutic candidate for the treatment of oral mucosal malignancies.
AB - Background Saussurea lappa , a plant used in traditional medicine, has shown promise in cancer treatment This study aimed to evaluate the therapeutic efficacy of Saussurea lappa nanoparticles using immunohistochemical analysis in a benzo[ a ]pyrene-induced mouse model of oral squamous cell carcinoma (OSCC). The investigation focused on the expression of markers related to apoptosis (Bax, Caspase-3, BCL-2), inflammation (TNF-α), proliferation (Ki-67), and tumor suppression (p53). Methods A true experimental design was employed using male Mus musculus mice. OSCC was induced via exposure to benzo[ a ]pyrene. Following induction, mice were treated perorally with Saussurea lappa nanoparticles at doses of 50, 100, and 200 mg/kg body weight, while the control group received CMC-Na. Buccal mucosa samples were collected for immunohistochemical analysis, assessing dose-dependent effects of Saussurea lappa nanoparticles on the expression of Bax, Caspase-3, BCL-2, TNF-α, Ki-67 and p53. Result Saussurea lappa nanoparticles demonstrated dose-dependent therapeutic effects in the OSCC mouse model. They significantly upregulated Bax, Caspase-3, TNF-α, and p53, while downregulating BCL-2 and Ki-67expression. The highest dose (200 mg/kg) showed the most pronounced effects, indicating enhanced apoptosis, reduced proliferation, and modulation of the inflammatory environment. Conclusion These findings suggest that Saussurea lappa nanoparticles, particularly at a dose of 200 mg/kg BW, effectively promote apoptosis, inhibit cell proliferation, and suppress anti-apoptotic pathways. This highlights their potential as a promising therapeutic candidate for the treatment of oral mucosal malignancies.
KW - Benzo[a]pyrene
KW - Nanoparticle
KW - Oral cancer
KW - Saussurea lappa
UR - https://www.scopus.com/pages/publications/105025437928
U2 - 10.1016/j.acthis.2025.152312
DO - 10.1016/j.acthis.2025.152312
M3 - Article
AN - SCOPUS:105025437928
SN - 0065-1281
VL - 128
JO - Acta Histochemica
JF - Acta Histochemica
IS - 1
M1 - 152312
ER -