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黄烷酮和2'-羟基黄烷酮通过下调蛋白酶活性和丝裂原活化蛋白激酶(MAPK)信号通路来抑制肺癌细胞的转移。

Flavanone and 2'-OH flavanone inhibit metastasis of lung cancer cells via down-regulation of proteinases activities and MAPK pathway.

作者信息

Hsiao Yung-Chin, Kuo Wu-Hsien, Chen Pei-Ni, Chang Horng-Rong, Lin Tseng-Hsi, Yang Wei-En, Hsieh Yih-Shou, Chu Shu-Chen

机构信息

Institute of Biochemistry and Biotechnology, Chung Shan Medical University, No. 110, Section 1, Chien Kuo N. Road, Taichung 402, Taiwan.

出版信息

Chem Biol Interact. 2007 May 1;167(3):193-206. doi: 10.1016/j.cbi.2007.02.012. Epub 2007 Feb 24.

Abstract

Flavanones richly exist in citrus and have been well characterized to have various bioactive properties. However, the anti-metastasis properties of flavanones remain unclear. The anti-metastatic effects of six flavanones including flavanone, 2'-OH flavanone, 4'-OH flavanone, 6-OH flavanone, naringin, and naringenin were investigated in lung cancer cells. Despite little influence on cell viability, flavanone and 2'-OH flavanone markedly inhibited the invasion, motility, and cell-matrix adhesion of A549 cells. This was associated with a reduced expression of matrix metalloproteinase (MMP)-2 and urokinase-type plasminogen activator (u-PA) in treated cells. Treatment with flavanone and 2'-OH flavanone also potently attenuated the phosphorylations of extracellular signal-regulated kinase 1/2 (ERK 1/2) and p38(MAPK), as well as the activations of NF-kappaB and AP-1. The reduced expressions of MMP-2 and u-PA, as well as inhibition of cell invasion were obtained in the cultures treated with U0126 (ERK 1/2 inhibitor) and SB203580 (p38(MAPK) inhibitor). Thus, the inhibitory effects of flavanone and 2'-OH flavanone on the expression of MMP-2 and u-PA may be at least partly through inactivation of ERK 1/2 and p38(MAPK) signaling pathways. Finally, oral administration of flavanone and 2'-OH flavanone were evidenced by its inhibition on the metastasis of A549 cells and Lewis lung carcinoma (LLC) cells in vivo. In conclusion, flavanone and 2'-OH flavanone perturb the invasion and metastasis of lung cancer cells, thereby constituting an adjuvant treatment for metastasis control.

摘要

黄烷酮大量存在于柑橘类水果中,其各种生物活性特性已得到充分表征。然而,黄烷酮的抗转移特性仍不清楚。研究了六种黄烷酮(包括黄烷酮、2'-羟基黄烷酮、4'-羟基黄烷酮、6-羟基黄烷酮、柚皮苷和柚皮素)对肺癌细胞的抗转移作用。尽管对细胞活力影响不大,但黄烷酮和2'-羟基黄烷酮显著抑制了A549细胞的侵袭、运动能力和细胞与基质的黏附。这与处理后细胞中基质金属蛋白酶(MMP)-2和尿激酶型纤溶酶原激活剂(u-PA)表达降低有关。用黄烷酮和2'-羟基黄烷酮处理还能有效减弱细胞外信号调节激酶1/2(ERK 1/2)和p38(丝裂原活化蛋白激酶)的磷酸化,以及核因子κB和活化蛋白-1的激活。在用U0126(ERK 1/2抑制剂)和SB203580(p38(丝裂原活化蛋白激酶)抑制剂)处理的培养物中,获得了MMP-2和u-PA表达降低以及细胞侵袭抑制的结果。因此,黄烷酮和2'-羟基黄烷酮对MMP-2和u-PA表达的抑制作用可能至少部分是通过ERK 1/2和p38(丝裂原活化蛋白激酶)信号通路的失活实现的。最后,黄烷酮和2'-羟基黄烷酮口服给药对体内A549细胞和Lewis肺癌(LLC)细胞转移的抑制作用得到了证实。总之,黄烷酮和2'-羟基黄烷酮扰乱肺癌细胞的侵袭和转移,从而构成一种控制转移的辅助治疗方法。

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