Antiproliferative effect of p-Coumaric acid targets UPR activation by downregulating Grp78 in colon cancer

被引:83
作者
Sharma, Sharada H. [1 ]
Rajamanickam, Vinothkumar [2 ]
Nagarajan, Sangeetha [1 ]
机构
[1] SASTRA Deemed Univ, Sch Chem & Biotechnol, Thanjavur 613401, Tamil Nadu, India
[2] Wenzhou Med Univ, Sch Pharmaceut Sci, Chem Biol Res Ctr, Wenzhou 325035, Zhejiang, Peoples R China
关键词
Cancer chemoprevention; Colon cancer; p-Coumaric acid; Grp78 (78 kDa glucose regulated protein); ER stress; Apoptosis; ENDOPLASMIC-RETICULUM STRESS; PROTEIN; 78; OVEREXPRESSION; EXPRESSION; INDUCTION; PATHWAY; METASTASIS; GROWTH; CELLS; GRP94;
D O I
10.1016/j.cbi.2018.06.001
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
p-CA is a naturally occurring phenolic acid present in most plants and in all commonly consumed vegetables and fruits. Here we demonstrated the anti-cancer effect of the food borne phytochemicalp-CA both in vitro and in vivo models of colon cancer using growth rate and tumor incidence as endpoints. Glucose regulated protein (GRP78) induction and UPR activation plays a key role in oncogenic progression, therefore increased dependence of cancer cells on these UPR signaling pathways for survival can be exploited for anti-cancer research. Hence we investigated the effect of p-CA on Grp78 a molecular chaperone often upregulated in colon cancer and its impact on unfolded protein response (UPR). Administration of the procarcinogen 1,2-dimethylhydrazine (DMH) causes Grp78 upregulation and tumor adaptation via UPR activation. The adaptive activity of UPR activates antiapoptotic NF-kappa B that results in upregulation of the markers of inflammation and angiogenesis. Supplementation of p-CA downregulated Grp78 and activated UPR mediated apoptosis both in in vitro and in vivo models of colon cancer. Further we observed that p-CA significantly reduced inflammation by decreasing the expression of cytokines COX-2, IL-6, TNF-alpha and PGE2 as analyzed by q-PCR and also reduced the expression of p-p65 and p-I kappa B alpha as analyzed by western blot. Further mechanistic insights revealed that p-CA inhibits Grp78 upregulation in cancer cells through activation of PERK-eIF2 alpha-ATF-4-CHOP pathway that culminates in apoptosis inducing effect of p-CA.
引用
收藏
页码:16 / 28
页数:13
相关论文
共 47 条
[1]   Esterase activity able to hydrolyze dietary antioxidant hydroxycinnamates is distributed along the intestine of mammals [J].
Andreasen, MF ;
Kroon, PA ;
Williamson, G ;
Garcia-Conesa, MT .
JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY, 2001, 49 (11) :5679-5684
[2]  
[Anonymous], GRP78 BIP INHIBITS E
[3]  
[Anonymous], TRENDS CANC
[4]   Global patterns and trends in colorectal cancer incidence and mortality [J].
Arnold, Melina ;
Sierra, Monica S. ;
Laversanne, Mathieu ;
Soerjomataram, Isabelle ;
Jemal, Ahmedin ;
Bray, Freddie .
GUT, 2017, 66 (04) :683-691
[5]   Biology of colorectal cancer [J].
Arvelo, Francisco ;
Sojo, Felipe ;
Cotte, Carlos .
ECANCERMEDICALSCIENCE, 2015, 9
[6]  
Chang Yaw-Wen, 2012, PLoS One, V7, pe38079, DOI [10.1371/journal.pone.0041362, 10.1371/journal.pone.0038079]
[7]   Glucose-regulated protein 78 (GRP78) regulates colon cancer metastasis through EMT biomarkers and the NRF-2/HO-1 pathway [J].
Chang, Yu-Jia ;
Chen, Wei-Yu ;
Huang, Chien-Yu ;
Liu, Hui-Hsiung ;
Wei, Po-Li .
TUMOR BIOLOGY, 2015, 36 (03) :1859-1869
[8]   COMBINATION CHEMOTHERAPY WITH 5-FLUOROURACIL (5FU) AND 1,3-BIS(2-CHLORO-ETHYL)-1-NITROSOUREA (BCNU) PROLONGS SURVIVAL OF RATS WITH DIMETHYLHYDRAZINE-INDUCED COLON CANCER [J].
DANZI, M ;
LEWIN, MR ;
CRUSE, JP ;
CLARK, CG .
GUT, 1983, 24 (11) :1041-1047
[9]   Aspirin and salicylate bind to immunoglobulin heavy chain binding protein (BiP) and inhibit its ATPase activity in human fibroblasts [J].
Deng, WG ;
Ruan, KH ;
Du, M ;
Saunders, MA ;
Wu, KK .
FASEB JOURNAL, 2001, 15 (13) :2463-2470
[10]  
DERENZINI M, 1990, LAB INVEST, V63, P137