TY - JOUR
T1 - Arnicolide D
T2 - a multi-targeted anticancer sesquiterpene lactone—preclinical efficacy and mechanistic insights
AU - Mangalpady, Shivaprasad Shetty
AU - Peña-Corona, Sheila I.
AU - Borbolla-Jiménez, Fabiola
AU - Kaverikana, Rajesh
AU - Shetty, Shobhitha
AU - Shet, Vinayaka Babu
AU - Almarhoon, Zainab M.
AU - Calina, Daniela
AU - Leyva-Gómez, Gerardo
AU - Sharifi-Rad, Javad
N1 - Publisher Copyright:
© The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature 2024.
PY - 2024/9
Y1 - 2024/9
N2 - Arnicolide D, a potent sesquiterpene lactone from Centipeda minima, has emerged as a promising anticancer candidate, demonstrating significant efficacy in inhibiting cancer cell proliferation, inducing apoptosis, and suppressing metastasis across various cancer models. This comprehensive study delves into the molecular underpinnings of Arnicolide D’s anticancer actions, emphasizing its impact on key signaling pathways such as PI3K/AKT/mTOR and STAT3, and its role in modulating cell cycle and survival mechanisms. Quantitative data from preclinical studies reveal Arnicolide D’s dose-dependent cytotoxicity against cancer cell lines, including nasopharyngeal carcinoma, triple-negative breast cancer, and human colon carcinoma, showcasing its broad-spectrum anticancer potential. Given its multifaceted mechanisms and preclinical efficacy, Arnicolide D warrants further investigation in clinical settings to validate its therapeutic utility against cancer. The evidence presented underscores the need for rigorous pharmacokinetic and toxicological studies to establish safe dosing parameters for future clinical trials.
AB - Arnicolide D, a potent sesquiterpene lactone from Centipeda minima, has emerged as a promising anticancer candidate, demonstrating significant efficacy in inhibiting cancer cell proliferation, inducing apoptosis, and suppressing metastasis across various cancer models. This comprehensive study delves into the molecular underpinnings of Arnicolide D’s anticancer actions, emphasizing its impact on key signaling pathways such as PI3K/AKT/mTOR and STAT3, and its role in modulating cell cycle and survival mechanisms. Quantitative data from preclinical studies reveal Arnicolide D’s dose-dependent cytotoxicity against cancer cell lines, including nasopharyngeal carcinoma, triple-negative breast cancer, and human colon carcinoma, showcasing its broad-spectrum anticancer potential. Given its multifaceted mechanisms and preclinical efficacy, Arnicolide D warrants further investigation in clinical settings to validate its therapeutic utility against cancer. The evidence presented underscores the need for rigorous pharmacokinetic and toxicological studies to establish safe dosing parameters for future clinical trials.
KW - Anti-cancer mechanisms
KW - Apoptosis
KW - Arnicolide D
KW - Centipeda minima
KW - PI3K/AKT/mTOR pathway
KW - Sesquiterpene lactone, Src degradation
UR - https://www.scopus.com/pages/publications/85191046568
U2 - 10.1007/s00210-024-03095-7
DO - 10.1007/s00210-024-03095-7
M3 - Artículo de revisión
C2 - 38652277
AN - SCOPUS:85191046568
SN - 0028-1298
VL - 397
SP - 6317
EP - 6336
JO - Naunyn-Schmiedeberg's Archives of Pharmacology
JF - Naunyn-Schmiedeberg's Archives of Pharmacology
IS - 9
ER -