Garcioligantone J and K, a pair of epimeric caged-polyprenylated xanthonoids from Garcinia Oligantha, inhibit the growth of lung cancer cells through ER stress-mediated apoptosis

Lingyu Li , Hao Zheng , Qingying Liu , Dongmei Ren
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Abstract

Garcioligantone J and K (GLJ and GLK) are a pair of isomers isolated from Garcinia Oligantha Merr. Herein, we described the structure elucidation including the absolute configurations of GLJ and GLK, explored and compared their anti-cancerous effects and underlying mechanism in A549 and NCI-H292 ​cells. The results indicated that GLJ and GLK are two isomers with different configuration at C-12, they inhibited cell proliferation and induced apoptosis in two lung cancer cell lines with almost the same extent. The induction of apoptosis by GLJ and GLK was demonstrated by DAPI and annexin-V-FITC/PI staining. Further investigation revealed increased Bax/Bcl-2 ratio, cleaved caspase-3, caspase-9 and PARP, loss of mitochondrial membrane potential (MMP) in cells, indicating that GLJ and GLK induced mitochondrial apoptosis. Increased GRP78, p-eIF2α and GADD153 manifested that endoplasmic reticulum (ER) stress was induced by GLJ and GLK. Meanwhile, upregulated reactive oxygen species (ROS) level was found and GLJ and GLK-induced ER stress and apoptosis could be attenuated by ROS scavenger NAC. Apoptosis induced by GLJ and GLK also could be alleviated by ER stress inhibitor 4-PBA. These showed that GLJ and GLK-induced apoptosis was mediated by ER stress relied on ROS generation. The efficacy of GLJ and GLK on lung cancer cell proliferation was further demonstrated in a zebrafish xenograft model. Collectively, the absolute configurations of GLJ and GLK were identified and they exerted lethal effects on lung cancer cells to the same extent via ROS-ER stress-mitochondrial apoptosis signaling, suggesting that GLJ and GLK might be used as potential modulating agents in lung cancer treatments.
Garcioligantone J和K是一对来自于Garcinia Oligantha的笼状聚戊烯基黄嘌呤类化合物,它们通过内质网应激介导的凋亡抑制肺癌细胞的生长
Garcioligantone J和K (GLJ和GLK)是从Garcinia Oligantha Merr中分离得到的一对异构体。本文对GLJ和GLK在A549和NCI-H292细胞中的绝对构型进行了结构解析,并对其抗癌作用和机制进行了探讨和比较。结果表明,GLJ和GLK是两种C-12位构型不同的异构体,它们在两种肺癌细胞系中抑制细胞增殖和诱导细胞凋亡的程度几乎相同。DAPI和annexin-V-FITC/PI染色证实GLJ和GLK诱导细胞凋亡。进一步研究发现,细胞中Bax/Bcl-2比值升高,caspase-3、caspase-9和PARP断裂,线粒体膜电位(MMP)丧失,表明GLJ和GLK诱导了线粒体凋亡。GRP78、p-eIF2α和GADD153升高表明GLJ和GLK诱导内质网(ER)应激。同时发现活性氧(ROS)水平上调,ROS清除剂NAC可减轻GLJ和glk诱导的内质网应激和凋亡。内质网应激抑制剂4-PBA也能减轻GLJ和GLK诱导的细胞凋亡。这表明GLJ和glk诱导的细胞凋亡是由内质网应激介导的,依赖于ROS的产生。GLJ和GLK对肺癌细胞增殖的影响在斑马鱼异种移植模型中得到进一步证实。总的来说,GLJ和GLK的绝对构型被确定,它们通过ROS-ER应激-线粒体凋亡信号对肺癌细胞产生相同程度的致死作用,提示GLJ和GLK可能作为潜在的肺癌治疗调节剂。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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