Methanolic Extracts of Solieria robusta Inhibits Proliferation of Oral Cancer Ca9-22 Cells via Apoptosis and Oxidative Stress

被引:37
|
作者
Yen, Yii-Huei [1 ]
Farooqi, Ammad Ahmad [2 ]
Li, Kun-Tzu [3 ]
Butt, Ghazala [4 ]
Tang, Jen-Yang [5 ,6 ,7 ,8 ]
Wu, Chang-Yi [9 ]
Cheng, Yuan-Bin [10 ]
Hou, Ming-Feng [5 ,11 ,12 ]
Chang, Hsueh-Wei [3 ,5 ,13 ,14 ]
机构
[1] Ten Chan Gen Hosp, Dept Dent, Chungli 32043, Taiwan
[2] Rashid Latif Med Coll, Lab Translat Oncol & Personalized Med, Lahore 54000, Pakistan
[3] Kaohsiung Med Univ, Dept Biomed Sci & Environm Biol, Kaohsiung 80708, Taiwan
[4] Govt Coll Univ, Dept Bot, Lahore 54000, Pakistan
[5] Kaohsiung Med Univ, Kaohsiung Med Univ Hosp, Ctr Canc, Kaohsiung 80708, Taiwan
[6] Kaohsiung Med Univ, Dept Radiat Oncol, Coll Med, Fac Med, Kaohsiung 80708, Taiwan
[7] Kaohsiung Med Univ Hosp, Dept Radiat Oncol, Kaohsiung 80708, Taiwan
[8] Kaohsiung Municipal Tatung Hosp, Dept Radiat Oncol, Kaohsiung 80145, Taiwan
[9] Natl Sun Yat Sen Univ, Dept Biol Sci, Kaohsiung 80424, Taiwan
[10] Kaohsiung Med Univ, Grad Inst Nat Prod, Coll Pharm, Kaohsiung 80708, Taiwan
[11] Kaohsiung Med Univ, Inst Clin Med, Kaohsiung 80708, Taiwan
[12] Kaohsiung Municipal Tatung Hosp, Dept Surg, Kaohsiung 80145, Taiwan
[13] Natl Sun Yat Sen Univ, Inst Med Sci & Technol, Kaohsiung 80424, Taiwan
[14] Kaohsiung Med Univ, Res Ctr Excellence Environm Med, Kaohsiung 80708, Taiwan
来源
MOLECULES | 2014年 / 19卷 / 11期
关键词
red alga; oral cancer; apoptosis; ROS; mitochondrial depolarization; DNA-DAMAGE; ANTIPROLIFERATIVE ACTIVITIES; GRACILARIA-TENUISTIPITATA; ANTIOXIDANTS; SEAWEED;
D O I
10.3390/molecules191118721
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Many red algae-derived natural products are known to have anticancer effects. The biological functions of the red alga Solieria robusta from the Karachi coast (Pakistan) remain unclear. Here, we prepared a methanolic extracts of S. robusta (MESR) to examine its possible anti-oral cancer effects and the corresponding mechanism of action. Cell viability of MESR-incubated oral cancer Ca9-22 cells was dose-responsively decreased (p < 0.001). According to a propidium iodide (PI)-based assay the cell cycle distribution was dramatically changed, especially for subG1 accumulation. Annexin V/PI assay of apoptosis using flow cytometry also showed that MESR-incubated Ca9-22 cells were dose-responsively increased (p < 0.001). For evaluation of oxidative stress in MESR-incubated Ca9-22 cells, we found that reactive oxygen species (ROS) were overexpressed dose-and time-responsively and mitochondrial depolarization was also increased (p < 0.001). Taken together, MESR showed inhibitory effects on oral cancer proliferation coupled with apoptosis and oxidative stress.
引用
收藏
页码:18721 / 18732
页数:12
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