2012
DOI: 10.1016/j.mrgentox.2012.06.003
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Antiproliferative effects of goniothalamin on Ca9-22 oral cancer cells through apoptosis, DNA damage and ROS induction

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Cited by 64 publications
(56 citation statements)
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“…Results showed that treatment with extract alters the level of Bax and Bcl-2 genes and induced high level of ROS in cells which points that reactive oxygen species may be responsible for induction of apoptosis. Growth inhibitory potential of goniothalamin on the Ca9-22 oral cancer cell line were tested by Yen et al (2012). Results obtained from this study demonstrated that goniothalamin inhibited growth via ROS induction, DNA damage and mitochondria dysfunction and further studies are required to tap the potential of goniothalamin for the development of a drug against oral cancer.…”
Section: Phytoconstituents As Ros Inducersmentioning
confidence: 94%
“…Results showed that treatment with extract alters the level of Bax and Bcl-2 genes and induced high level of ROS in cells which points that reactive oxygen species may be responsible for induction of apoptosis. Growth inhibitory potential of goniothalamin on the Ca9-22 oral cancer cell line were tested by Yen et al (2012). Results obtained from this study demonstrated that goniothalamin inhibited growth via ROS induction, DNA damage and mitochondria dysfunction and further studies are required to tap the potential of goniothalamin for the development of a drug against oral cancer.…”
Section: Phytoconstituents As Ros Inducersmentioning
confidence: 94%
“…GTN had been able to induce cytotoxicity in a variety of cancer cell lines including vascular smooth muscle cells (VSMCs), Chinese hamster ovary cells, renal cells [6971], hepatoblastoma [72, 73], gastric, kidney cells, breast carcinomas, leukemia, Jurkat cells [67, 69, 7484], hepatocellular carcinoma [85], lung cancer cells [86], oral cancer cells [87, 88], and HeLa cells [89, 90] but sparing the normal cells including blood cells [83]. …”
Section: Mechanism Of Actionmentioning
confidence: 99%
“…It is cytotoxic to and induces apoptosis in cancer cells such as cervical cancer (HeLa), breast carcinoma MCF-7 cell lines and colon cancer HT29 cells (Alabsi et al, 2012); Ca9-22 oral cancer cells (Yen et al, 2012); hepatoblastoma HepG2 cells (Al-Qubaisi et al, 2011); human lung cancer cells (Chiu et al, 2011); Jurkat T leukemia cells (Inayat-Hussain et al, 2010); and invasive breast carcinoma MDA-MB231 cell lines (Chen et al, 2005). It is also toxic to normal mouse fibroblast 3T3 cells (Alabsi et al, 2012), coronary artery smooth muscle cells , vascular smooth muscle cells (Chan et al, 2006).…”
Section: Introductionmentioning
confidence: 99%