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Down-regulation of cyclooxygenase-2 (cox-2) by cannabidiolic acid in human breast cancer cells

机译:大麻二酚酸对人乳腺癌细胞中环氧合酶-2(cox-2)的下调

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Metastases are known to be responsible for approximately 90% of breast cancer-related deaths. Cyclooxygenase-2 (COX-2) is involved not only in inflammatory processes, but also in the metastasis of cancer cells; it is expressed in 40% of human invasive breast cancers. To comprehensively analyze the effects of cannabidiolic acid (CBDA), a selective COX-2 inhibitor found in the fiber-type canna-bis plant (Takeda et al., 2008), on COX-2 expression and the genes involved in metastasis, we performed a DNA microarray analysis of human breast cancer MDA-MB-231 cells, which are invasive breast cancer cells that express high levels of COX-2, treated with CBDA for 48 hr at 25 μM. The results obtained revealed that COX-2 and Id-1, a positive regulator of breast cancer metastasis, were down-regulated (0.19-fold and 0.52-fold, respectively), while SHARP1 (or BHLHE41), a suppressor of breast cancer metastasis, was up-regulated (1.72-fold) and CHIP (or STUB1) was unaffected (1.03-fold). These changes were confirmed by real-time RT-PCR analyses. Taken together, the results obtained here demonstrated that i) CBDA had dual inhibitory effects on COX-2 through down-regulation and enzyme inhibition, and ii) CBDA may possess the ability to suppress genes that are positively involved in the metastasis of cancer cells in vitro.
机译:已知转移引起大约90%的乳腺癌相关死亡。环氧合酶2(COX-2)不仅参与炎症过程,而且参与癌细胞的转移。它在40%的人类浸润性乳腺癌中表达。为了全面分析在纤维型大麻植物中发现的选择性COX-2抑制剂大麻二酚(CBDA)(Takeda et al。,2008)对COX-2表达和转移相关基因的影响,我们进行了人乳腺癌MDA-MB-231细胞的DNA芯片分析,人乳腺癌MDA-MB-231细胞是表达高水平COX-2的侵袭性乳腺癌细胞,用CBDA在25μM下处理48小时。获得的结果表明,乳腺癌转移的阳性调节剂COX-2和Id-1被下调(分别为0.19倍和0.52倍),而SHARP1(或BHLHE41)是乳腺癌转移的抑制因子。 ,上调(1.72倍)和CHIP(或STUB1)不受影响(1.03倍)。这些变化已通过实时RT-PCR分析得到证实。综上所述,此处获得的结果表明:i)CBDA通过下调和酶抑制作用对COX-2具有双重抑制作用,并且ii)CBDA可能具有抑制与癌细胞转移积极相关的基因的能力。体外。

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