2010
DOI: 10.1007/s10068-010-0189-5
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α-pinene triggers oxidative stress and related signaling pathways in A549 and HepG2 cells

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Cited by 23 publications
(12 citation statements)
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“…On the basis of the chemical composition, the monoterpenes myrcene and α-pinene were the most abundant compounds of PLEO, suggesting that the antiproliferative effects of PL might be possibly mediated by these two compounds. In accord, previous evidence indicated that myrcene and α-pinene might exert significant cytotoxic effects on different cancer cell lines [ 22 24 ]. Nevertheless, the involvement of other PLEO minor constituents should not be ruled out; indeed, the terpenes limonene, β-caryophyllene, and β-elemene have also shown significant anticancer activities both in vitro and in vivo models [ 9 ], indicating potential synergies among EO components.…”
Section: Discussionsupporting
confidence: 81%
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“…On the basis of the chemical composition, the monoterpenes myrcene and α-pinene were the most abundant compounds of PLEO, suggesting that the antiproliferative effects of PL might be possibly mediated by these two compounds. In accord, previous evidence indicated that myrcene and α-pinene might exert significant cytotoxic effects on different cancer cell lines [ 22 24 ]. Nevertheless, the involvement of other PLEO minor constituents should not be ruled out; indeed, the terpenes limonene, β-caryophyllene, and β-elemene have also shown significant anticancer activities both in vitro and in vivo models [ 9 ], indicating potential synergies among EO components.…”
Section: Discussionsupporting
confidence: 81%
“…When experiments were repeated in the presence of GSH as antioxidant, no intracellular ROS accumulation and no inhibition of cancer cell growth were observed in FTC-133 cells after PL administration, thus indicating that PLEO might act as antiproliferative agent in a ROS-dependent manner. In accord, several terpenic EO constituents, such as α-pinene and β-caryophyllene, have demonstrated to specifically induce the production of ROS within cancer cells without increasing oxidative stress in normal cells [ 22 , 25 ].…”
Section: Discussionmentioning
confidence: 99%
“…Hassan et al (2010) [26] suggested that α-terpineol inhibits tumor cell growth by a mechanism that involves inhibition of the NF-kB (nuclear factor kappa B). Jin et al (2010) [27] showed that α-pinene, also found in this study, triggered oxidative stress and related signaling pathways in the HepG2 and A549 tumor cells.…”
Section: Resultssupporting
confidence: 71%
“…Later, it was revealed in human hepatoma Bel-7402 cells that the proapoptotic effect of α-pinene is associated with induction of G2/M cell cycle arrest ( 63 ). In addition, α-pinene triggers oxidative stress signaling pathways in A549 and HepG2 cells ( 64 ). However, Kusuhara et al .…”
Section: Terpenes and Tumormentioning
confidence: 99%