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茯苓酸通过靶向内质网应激在体外和体内抑制胰腺癌的生长并诱导其凋亡。

Pachymic acid inhibits growth and induces apoptosis of pancreatic cancer in vitro and in vivo by targeting ER stress.

作者信息

Cheng Shujie, Swanson Kristen, Eliaz Isaac, McClintick Jeanette N, Sandusky George E, Sliva Daniel

机构信息

Cancer Research Laboratory, Methodist Research Institute, Indiana University Health, Indianapolis, Indiana, United States of America.

Amitabha Medical Clinic and Healing Center, Santa Rosa, California, United States of America.

出版信息

PLoS One. 2015 Apr 27;10(4):e0122270. doi: 10.1371/journal.pone.0122270. eCollection 2015.

Abstract

Pachymic acid (PA) is a purified triterpene extracted from medicinal fungus Poria cocos. In this paper, we investigated the anticancer effect of PA on human chemotherapy resistant pancreatic cancer. PA triggered apoptosis in gemcitabine-resistant pancreatic cancer cells PANC-1 and MIA PaCa-2. Comparative gene expression array analysis demonstrated that endoplasmic reticulum (ER) stress was induced by PA through activation of heat shock response and unfolded protein response related genes. Induced ER stress was confirmed by increasing expression of XBP-1s, ATF4, Hsp70, CHOP and phospho-eIF2α. Moreover, ER stress inhibitor tauroursodeoxycholic acid (TUDCA) blocked PA induced apoptosis. In addition, 25 mg kg-1 of PA significantly suppressed MIA PaCa-2 tumor growth in vivo without toxicity, which correlated with induction of apoptosis and expression of ER stress related proteins in tumor tissues. Taken together, growth inhibition and induction of apoptosis by PA in gemcitabine-resistant pancreatic cancer cells were associated with ER stress activation both in vitro and in vivo. PA may be potentially exploited for the use in treatment of chemotherapy resistant pancreatic cancer.

摘要

茯苓酸(PA)是从药用真菌茯苓中提取的一种纯化三萜。在本文中,我们研究了PA对人化疗耐药性胰腺癌的抗癌作用。PA诱导吉西他滨耐药的胰腺癌细胞PANC-1和MIA PaCa-2发生凋亡。比较基因表达阵列分析表明,PA通过激活热休克反应和未折叠蛋白反应相关基因诱导内质网(ER)应激。通过增加XBP-1s、ATF4、Hsp70、CHOP和磷酸化eIF2α的表达证实了诱导的ER应激。此外,ER应激抑制剂牛磺熊去氧胆酸(TUDCA)阻断了PA诱导的凋亡。另外,25 mg kg-1的PA在体内显著抑制MIA PaCa-2肿瘤生长且无毒性,这与肿瘤组织中凋亡的诱导和ER应激相关蛋白的表达有关。综上所述,PA在吉西他滨耐药的胰腺癌细胞中抑制生长和诱导凋亡与体内外ER应激激活有关。PA可能具有用于治疗化疗耐药性胰腺癌的潜在价值。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dc2a/4411097/41d28ce8f2d9/pone.0122270.g001.jpg

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