The mechanism of curcumin’s anti- cancer activity is not complete

The mechanism of curcumin’s anti- cancer activity is not completely revealed though. This study was aimed to investigate the possible mechanism of curcumin’s

effects on N- methyl- N- nitrosourea (MNU) induced gastric cancer in rats. Methods: Male wistar rats were divided into 4 groups: Ctrl: control group; MNU: rats treated by MNU intragastrically; MNU+CUR: rats treated by MNU administration supplemented with curcumin intragastrically; MNU+CUR+PBA: rats treated by MNU and curcumin administration pretreated by 4- phenylbutyrate (4-PBA) intraperitoneally. Gastric cancer tissue was harvested from sacrificed rats. Reactive stress spices Ibrutinib in vivo (ROS) were detected by DHE staining. A TUNEL assay was used to evaluate apoptosis of gastric cancer cells. Real- time PCR and Western blotting were used to determine the activation of endoplasmic reticulum (ER) stress. Results: Excessive generation of ROS was induced by curcumin in MNU+CUR, MNU+CUR+PBA compared with Ctrl and MNU. Cancer cell apoptosis in MNU+CUR increased significantly

compared with MNU and MNU+CUR+PBA. Elevated expressions of GRP78 and CHOP were confirmed by Real- time PCR and Western blotting. Increased expression of activation of Caspase-12 (in a cleaved form) was examined by Western blotting. GRP78 and CHOP are key molecules in ER stress signal transmission, while Caspase-12 is referred as an ER- stress specific indicator of apoptosis. These results indicated that during Silmitasertib price MNU- induced gastric carcinoma, ER stress was activated by curcumin- induced ROS generation, taking responsibility for cancer cell apoptosis. 4-PBA (ER stress inhibitor)’s protective effect against cancer cell apoptosis confirmed the involvement of ROS- medicated ER stress in curcumin’s therapeutic effects in gastric carcinoma. Conclusion: ROS induced ER stress plays an important

role in curcumin induced gastric cancer cell apoptosis Key Word(s): 1. curcumin; 2. gastric carcinoma; 3. apoptosis; Presenting Author: XIN XU Additional Authors: ZHONGWEI LIU, KUNLUN CHEN, ZHIKAI ZHANG, YING LIU, JIE LI, JIANGYI CAI, YI YANG, JINKAI XU, JIE WU Corresponding Author: XIN XU Affiliations: The Second Affiliated Hospital, School of Medicine, Xi’an Jiaotong University; Xi’an Aerospace General check details Hospital Objective: PERK (protein kinase RNA – like ER kinase)/ eIF2α (eukaryotic translation initiation factor 2 alpha)/ ATF4 (activating transcription factor 4)/ CHOP is an important signaling pathway conducting apoptotic signals in endoplasmic reticulum (ER) stress. It is suggested that curcumin induces apoptosis of cancer cells in several studies and our previous work. This study is aimed to investigate whether curcumin enhances chemosensitivity of 5- fluorouracil (5-FU) in gastric cancer and to explore its possible mechanism. Methods: Equal amount SGC-7901 cells were divided into Ctrl (control), FU (treated by 5-FU), CUR (treated by curcumin) and FU+CUR (co-administrated by curcumin and 5-FU).

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