Alantolactone, a sesquiterpene lactone isolated from Inula helenium L. selectively suppresses STAT3 activation and exhibits anticancer activity in MDA-MB-231 cells

Planta Medica ◽  
2015 ◽  
Vol 81 (16) ◽  
Author(s):  
J Chun ◽  
YS Kim
2018 ◽  
Vol 106 ◽  
pp. 239-246 ◽  
Author(s):  
Ghader babaei ◽  
Azadeh Aliarab ◽  
Sina Abroon ◽  
Yusof Rasmi ◽  
Shiva Gholizadeh- Ghaleh Aziz

2008 ◽  
Vol 18 (14) ◽  
pp. 4015-4017 ◽  
Author(s):  
A. Robinson ◽  
T. Vijay Kumar ◽  
E. Sreedhar ◽  
V.G.M. Naidu ◽  
Sistla Rama Krishna ◽  
...  

2020 ◽  
Vol 20 (9) ◽  
pp. 666-674
Author(s):  
Margarita E. Neganova ◽  
Sergey G. Klochkov ◽  
Sergey A. Pukhov ◽  
Svetlana V. Afanasieva ◽  
Yulia R. Aleksandrova ◽  
...  

Background: The conjugates of the sesquiterpene lactone of the eremophilane series of 6- hydroxyxanthanodiene with hydrogenated azines (piperidines and piperazines) have been synthesized and identified by NMR spectrometer. Objective: A lactone with an unusual skeleton “6-hydroxyxanthanodiene” was extracted from the plant Elecampane (Inula helenium L) and identified various species with NMR spectrometer. Methods: The cytotoxic, mitochondrial, and antioxidant activities on different tumor lines such as A549, HCT116, RD and Jurkat were investigated and determined possible mechanisms. Results: The results showed that the most potent compound was IIIi exhibiting highest cytotoxicity against RD cells (IC50 25.23 ± 0.04 μM), depolarized the mitochondrial membrane and was an effective antioxidant (IC50 inhibition of LP 10.68 ± 3.21 μM) without any toxic side effect on healthy cells. Conclusion: The conjugates of sesquiterpene lactone 6-hydroxyxanthanodiene III and hydrogenated azines may help to design potential promising anticancer drugs.


2019 ◽  
Vol 10 (7) ◽  
pp. 4143-4152 ◽  
Author(s):  
Shoujiao Peng ◽  
Yanan Hou ◽  
Juan Yao ◽  
Jianguo Fang

Costunolide (COS), a natural sesquiterpene lactone originally isolated from Inula helenium (Compositae), shows potent neuroprotective effects against oxidative stress-mediated injuries of PC12 cells via activating transcription factor Nrf2.


2013 ◽  
Vol 2013 ◽  
pp. 1-9 ◽  
Author(s):  
Azhar Rasul ◽  
Muhammad Khan ◽  
Muhammad Ali ◽  
Jiang Li ◽  
Xiaomeng Li

Alantolactone and isoalantolactone, main bioactive compounds that are present in many medicinal plants such asInula helenium, L. Inula japonica, Aucklandia lappa, Inula racemosa,andRadix inulae, have been found to have various pharmacological actions including anti-inflammatory, antimicrobial, and anticancer properties, with no significant toxicity. Recently, the anticancer activity of alantolactone and isoalantolactone has been extensively investigated. Here, our aim is to review their natural sources and their anticancer activity with specific emphasis on mechanism of actions, by which these compounds act on apoptosis pathways. Based on the literature and also on our previous results, alantolactone and isoalantolactone induce apoptosis by targeting multiple cellular signaling pathways that are frequently deregulated in cancers and suggest that their simultaneous targeting by these compounds could result in efficacious and selective killing of cancer cells. This review suggests that alantolactone and isoalantolactone are potential promising anticancer candidates, but additional studies and clinical trials are required to determine their specific intracellular sites of actions and derivative targets in order to fully understand the mechanisms of therapeutic effects to further validate in cancer chemotherapy.


Author(s):  
Mahpara Qadir ◽  
Nissar A Dangroo ◽  
Syed Wajaht Amin Shah

Objective: In the present study, the extracts (petroleum ether and methanolic extract) of plant Artemisia maritima were subjected to bioactivity evaluation and compound isolation and characterization.Methods: Antioxidant activity was carried out using ferric reducing power and 2,2-diphenyl-1-picrylhydrazyl (DPPH) assay. The anticancer activity was evaluated by MTT assay using three different human cancer cell lines: Embryonic kidney cancer cell (HEK), lung adenocarcinoma epithelial cell (A-549), and human colon cancer cell (HCT), and isolated compounds were characterized using nuclear magnetic resonance (1HNMR), 13CNMR, DEPT, infrared, and mass spectroscopic techniques.Results: The petroleum ether extract of the plant displayed significant antioxidant and cytotoxic effects, which on phytochemical analysis led to the isolation of two bioactive sesquiterpene lactone compounds. These phytochemicals were identified using different spectral techniques in the light of literature. All the compounds displayed significant cytotoxic activity; however, compound-1 exhibited potent anticancer activity with inhibitory concentration value of 17.3 μg/mL. The isolated compounds also displayed significant antioxidant potential.Conclusion: Artemisia maritima, a rich source of sesquiterpene lactone which may be responsible for significant anticancer potential and it also possess remarkable antioxidant activity and hence may be of immense importance to food Chemistry.


2010 ◽  
Vol 20 (1) ◽  
pp. 21-34 ◽  
Author(s):  
Karolina Lesiak ◽  
Kamila Koprowska ◽  
Izabela Zalesna ◽  
Dariusz Nejc ◽  
Markus Düchler ◽  
...  

Author(s):  
Mahpara Qadir ◽  
Nissar A Dangroo ◽  
Syed Wajaht Amin Shah

Objective: In the present study, the extracts (petroleum ether and methanolic extract) of plant Artemisia maritima were subjected to bioactivity evaluation and compound isolation and characterization.Methods: Antioxidant activity was carried out using ferric reducing power and 2,2-diphenyl-1-picrylhydrazyl (DPPH) assay. The anticancer activity was evaluated by MTT assay using three different human cancer cell lines: Embryonic kidney cancer cell (HEK), lung adenocarcinoma epithelial cell (A-549), and human colon cancer cell (HCT), and isolated compounds were characterized using nuclear magnetic resonance (1HNMR), 13CNMR, DEPT, infrared, and mass spectroscopic techniques.Results: The petroleum ether extract of the plant displayed significant antioxidant and cytotoxic effects, which on phytochemical analysis led to the isolation of two bioactive sesquiterpene lactone compounds. These phytochemicals were identified using different spectral techniques in the light of literature. All the compounds displayed significant cytotoxic activity; however, compound-1 exhibited potent anticancer activity with inhibitory concentration value of 17.3 μg/mL. The isolated compounds also displayed significant antioxidant potential.Conclusion: Artemisia maritima, a rich source of sesquiterpene lactone which may be responsible for significant anticancer potential and it also possess remarkable antioxidant activity and hence may be of immense importance to food Chemistry.


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