Rotundifuran Induces Ferroptotic Cell Death and Mitochondria Permeability Transition in Lung Cancer Cells
Rotundifuran (RF), a potent anti-inflammatory and anti-cancer compound, is a natural compound predominantly present in Vitex Rotundifolia. Herein, we investigated the effects of RF on the growth of lung cancer cells. Our findings suggested that RF inhibits cell growth, highlighting its potential as a therapeutic agent for cancer treatment. Interestingly, we observed that cell growth inhibition was not due to apoptosis, as caspases were not activated and DNA fragmentation did not occur. Furthermore, we found that intracellular vacuoles and autophagy were induced, but RF-induced cell death was not affected when autophagy was inhibited. This prompted us to investigate other possible mechanisms underlying cell growth inhibition. Through a cDNA chip analysis, we confirmed changes in the expression of ferroptosis-related genes and observed lipid peroxidation. We further examined the effect of ferroptosis inhibitors and found that they alleviated cell growth inhibition induced by RF. We also observed the involvement of calcium signaling, ROS accumulation, and JNK signaling in the induction of ferroptosis. Our findings suggested that RF is a potent anti-cancer drug and further studies are needed to validate its clinal use.
Medienart: |
E-Artikel |
---|
Erscheinungsjahr: |
2024 |
---|---|
Erschienen: |
2024 |
Enthalten in: |
Zur Gesamtaufnahme - volume:12 |
---|---|
Enthalten in: |
Biomedicines - 12(2024), 3 vom: 05. März |
Sprache: |
Englisch |
---|
Beteiligte Personen: |
Kang, Myung-Ji [VerfasserIn] |
---|
Links: |
---|
Themen: |
Ferroptosis |
---|
Anmerkungen: |
Date Revised 30.03.2024 published: Electronic Citation Status PubMed-not-MEDLINE |
---|
doi: |
10.3390/biomedicines12030576 |
---|
funding: |
|
---|---|
Förderinstitution / Projekttitel: |
|
PPN (Katalog-ID): |
NLM370297326 |
---|
LEADER | 01000caa a22002652 4500 | ||
---|---|---|---|
001 | NLM370297326 | ||
003 | DE-627 | ||
005 | 20240331001532.0 | ||
007 | cr uuu---uuuuu | ||
008 | 240329s2024 xx |||||o 00| ||eng c | ||
024 | 7 | |a 10.3390/biomedicines12030576 |2 doi | |
028 | 5 | 2 | |a pubmed24n1357.xml |
035 | |a (DE-627)NLM370297326 | ||
035 | |a (NLM)38540189 | ||
035 | |a (PII)576 | ||
040 | |a DE-627 |b ger |c DE-627 |e rakwb | ||
041 | |a eng | ||
100 | 1 | |a Kang, Myung-Ji |e verfasserin |4 aut | |
245 | 1 | 0 | |a Rotundifuran Induces Ferroptotic Cell Death and Mitochondria Permeability Transition in Lung Cancer Cells |
264 | 1 | |c 2024 | |
336 | |a Text |b txt |2 rdacontent | ||
337 | |a ƒaComputermedien |b c |2 rdamedia | ||
338 | |a ƒa Online-Ressource |b cr |2 rdacarrier | ||
500 | |a Date Revised 30.03.2024 | ||
500 | |a published: Electronic | ||
500 | |a Citation Status PubMed-not-MEDLINE | ||
520 | |a Rotundifuran (RF), a potent anti-inflammatory and anti-cancer compound, is a natural compound predominantly present in Vitex Rotundifolia. Herein, we investigated the effects of RF on the growth of lung cancer cells. Our findings suggested that RF inhibits cell growth, highlighting its potential as a therapeutic agent for cancer treatment. Interestingly, we observed that cell growth inhibition was not due to apoptosis, as caspases were not activated and DNA fragmentation did not occur. Furthermore, we found that intracellular vacuoles and autophagy were induced, but RF-induced cell death was not affected when autophagy was inhibited. This prompted us to investigate other possible mechanisms underlying cell growth inhibition. Through a cDNA chip analysis, we confirmed changes in the expression of ferroptosis-related genes and observed lipid peroxidation. We further examined the effect of ferroptosis inhibitors and found that they alleviated cell growth inhibition induced by RF. We also observed the involvement of calcium signaling, ROS accumulation, and JNK signaling in the induction of ferroptosis. Our findings suggested that RF is a potent anti-cancer drug and further studies are needed to validate its clinal use | ||
650 | 4 | |a Journal Article | |
650 | 4 | |a ferroptosis | |
650 | 4 | |a mitochondria permeability transition (MPT) | |
650 | 4 | |a reactive oxygen species (ROS) | |
650 | 4 | |a rotundifuran | |
700 | 1 | |a Moon, Dong-Oh |e verfasserin |4 aut | |
700 | 1 | |a Park, Ji-Yoon |e verfasserin |4 aut | |
700 | 1 | |a Kim, Namho |e verfasserin |4 aut | |
700 | 1 | |a Lee, Su Hyeon |e verfasserin |4 aut | |
700 | 1 | |a Ryu, Hyung Won |e verfasserin |4 aut | |
700 | 1 | |a Huh, Yang Hoon |e verfasserin |4 aut | |
700 | 1 | |a Lee, Hyun-Sun |e verfasserin |4 aut | |
700 | 1 | |a Kim, Mun-Ock |e verfasserin |4 aut | |
773 | 0 | 8 | |i Enthalten in |t Biomedicines |d 2013 |g 12(2024), 3 vom: 05. März |w (DE-627)NLM268899797 |x 2227-9059 |7 nnns |
773 | 1 | 8 | |g volume:12 |g year:2024 |g number:3 |g day:05 |g month:03 |
856 | 4 | 0 | |u http://dx.doi.org/10.3390/biomedicines12030576 |3 Volltext |
912 | |a GBV_USEFLAG_A | ||
912 | |a GBV_NLM | ||
951 | |a AR | ||
952 | |d 12 |j 2024 |e 3 |b 05 |c 03 |