Pomegranate Extract (POMx) Induces Mitochondrial Dysfunction and Apoptosis of Oral Cancer Cells
The anticancer effect of pomegranate polyphenolic extract POMx in oral cancer cells has rarely been explored, especially where its impact on mitochondrial functioning is concerned. Here, we attempt to evaluate the proliferation modulating function and mechanism of POMx against human oral cancer (Ca9-22, HSC-3, and OC-2) cells. POMx induced ATP depletion, subG1 accumulation, and annexin V/Western blotting-detected apoptosis in these three oral cancer cell lines but showed no toxicity to normal oral cell lines (HGF-1). POMx triggered mitochondrial membrane potential (MitoMP) disruption and mitochondrial superoxide (MitoSOX) generation associated with the differential downregulation of several antioxidant gene mRNA/protein expressions in oral cancer cells. POMx downregulated mitochondrial mass, mitochondrial DNA copy number, and mitochondrial biogenesis gene mRNA/protein expression in oral cancer cells. Moreover, POMx induced both PCR-based mitochondrial DNA damage and γH2AX-detected nuclear DNA damage in oral cancer cells. In conclusion, POMx provides antiproliferation and apoptosis of oral cancer cells through mechanisms of mitochondrial impairment..
Medienart: |
E-Artikel |
---|
Erscheinungsjahr: |
2021 |
---|---|
Erschienen: |
2021 |
Enthalten in: |
Zur Gesamtaufnahme - volume:10 |
---|---|
Enthalten in: |
Antioxidants - 10(2021), 7, p 1117 |
Sprache: |
Englisch |
---|
Beteiligte Personen: |
Sheng-Yao Peng [VerfasserIn] |
---|
Links: |
doi.org [kostenfrei] |
---|
Themen: |
Apoptosis |
---|
doi: |
10.3390/antiox10071117 |
---|
funding: |
|
---|---|
Förderinstitution / Projekttitel: |
|
PPN (Katalog-ID): |
DOAJ056017405 |
---|
LEADER | 01000caa a22002652 4500 | ||
---|---|---|---|
001 | DOAJ056017405 | ||
003 | DE-627 | ||
005 | 20240412170503.0 | ||
007 | cr uuu---uuuuu | ||
008 | 230227s2021 xx |||||o 00| ||eng c | ||
024 | 7 | |a 10.3390/antiox10071117 |2 doi | |
035 | |a (DE-627)DOAJ056017405 | ||
035 | |a (DE-599)DOAJb09d6acbdcbc4a43953de73e6881c2d0 | ||
040 | |a DE-627 |b ger |c DE-627 |e rakwb | ||
041 | |a eng | ||
050 | 0 | |a RM1-950 | |
100 | 0 | |a Sheng-Yao Peng |e verfasserin |4 aut | |
245 | 1 | 0 | |a Pomegranate Extract (POMx) Induces Mitochondrial Dysfunction and Apoptosis of Oral Cancer Cells |
264 | 1 | |c 2021 | |
336 | |a Text |b txt |2 rdacontent | ||
337 | |a Computermedien |b c |2 rdamedia | ||
338 | |a Online-Ressource |b cr |2 rdacarrier | ||
520 | |a The anticancer effect of pomegranate polyphenolic extract POMx in oral cancer cells has rarely been explored, especially where its impact on mitochondrial functioning is concerned. Here, we attempt to evaluate the proliferation modulating function and mechanism of POMx against human oral cancer (Ca9-22, HSC-3, and OC-2) cells. POMx induced ATP depletion, subG1 accumulation, and annexin V/Western blotting-detected apoptosis in these three oral cancer cell lines but showed no toxicity to normal oral cell lines (HGF-1). POMx triggered mitochondrial membrane potential (MitoMP) disruption and mitochondrial superoxide (MitoSOX) generation associated with the differential downregulation of several antioxidant gene mRNA/protein expressions in oral cancer cells. POMx downregulated mitochondrial mass, mitochondrial DNA copy number, and mitochondrial biogenesis gene mRNA/protein expression in oral cancer cells. Moreover, POMx induced both PCR-based mitochondrial DNA damage and γH2AX-detected nuclear DNA damage in oral cancer cells. In conclusion, POMx provides antiproliferation and apoptosis of oral cancer cells through mechanisms of mitochondrial impairment. | ||
650 | 4 | |a pomegranate | |
650 | 4 | |a mitochondrial DNA | |
650 | 4 | |a DNA damage | |
650 | 4 | |a apoptosis | |
650 | 4 | |a oral cancer | |
653 | 0 | |a Therapeutics. Pharmacology | |
700 | 0 | |a Li-Ching Lin |e verfasserin |4 aut | |
700 | 0 | |a Shu-Rong Chen |e verfasserin |4 aut | |
700 | 0 | |a Ammad A. Farooqi |e verfasserin |4 aut | |
700 | 0 | |a Yuan-Bin Cheng |e verfasserin |4 aut | |
700 | 0 | |a Jen-Yang Tang |e verfasserin |4 aut | |
700 | 0 | |a Hsueh-Wei Chang |e verfasserin |4 aut | |
773 | 0 | 8 | |i In |t Antioxidants |d MDPI AG, 2013 |g 10(2021), 7, p 1117 |w (DE-627)DOAJ000099481 |x 20763921 |7 nnns |
773 | 1 | 8 | |g volume:10 |g year:2021 |g number:7, p 1117 |
856 | 4 | 0 | |u https://doi.org/10.3390/antiox10071117 |z kostenfrei |
856 | 4 | 0 | |u https://doaj.org/article/b09d6acbdcbc4a43953de73e6881c2d0 |z kostenfrei |
856 | 4 | 0 | |u https://www.mdpi.com/2076-3921/10/7/1117 |z kostenfrei |
856 | 4 | 2 | |u https://doaj.org/toc/2076-3921 |y Journal toc |z kostenfrei |
912 | |a GBV_USEFLAG_A | ||
912 | |a GBV_DOAJ | ||
951 | |a AR | ||
952 | |d 10 |j 2021 |e 7, p 1117 |