Curcumin and Gastric Cancer: a Review on Mechanisms of Action

被引:79
作者
Hassanalilou, Tohid [1 ]
Ghavamzadeh, Saeid [2 ]
Khalili, Leila [1 ]
机构
[1] Tabriz Univ Med Sci, Dept Nutr, Fac Nutr & Food Sci, Tabriz, Iran
[2] Urmia Univ Med Sci, Fac Med, Dept Human Nutr, Orumiyeh, Iran
关键词
Curcumin; Gastric cancer; Mechanisms; FACTOR-KAPPA-B; APOPTOTIC CELL-DEATH; PROSPECTIVE IDENTIFICATION; P21-ACTIVATED KINASES; MULTIDRUG-RESISTANCE; MEDIATED APOPTOSIS; INDUCE APOPTOSIS; P-GLYCOPROTEIN; COLON-CANCER; IN-VITRO;
D O I
10.1007/s12029-018-00186-6
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background and AimGastric cancer, as the fourth cause of death in women and third in men with malignant tumors, is now threatening people's lives worldwide. Natural anti-tumor products are potential anti-cancer agents with fewer by-effects. Curcumin, an herbal product, has been used as a cosmetic and food additive and as a traditional herbal medicine for thousands of years in Asian countries. Several studies revealed that curcumin can inhibit the invasion and proliferation of gastric cancer cells. This paper analyzes existing data from animal and in vitro studies in order to highlight the mechanisms of therapeutic effects of curcumin in gastric cancer.MethodsScience Direct and Pub Med databases were searched by using curcumin and gastric cancer for searching the studies aiming the application of curcumin and the beneficial effects of curcumin in gastric cancer control and treatment.ResultsThese results suggested that curcumin can suppress multiple signaling pathways and inhibit cancer cell proliferation, invasion, metastasis, and angiogenesis. According to the studies, curcumin can inhibit gastric cancer by several mechanisms including decreasing proliferation, inducing apoptosis, and reducing chemo-resistance in gastric cancer cells.ConclusionsThe findings of present paper provided novel perceptions about the mechanisms of curcumin action in gastric cancer cell growth inhibition and its therapeutic strategies for gastric cancer control. So, curcumin could be considered as a novel therapeutic strategy to control gastric cancer cell growth.
引用
收藏
页码:185 / 192
页数:8
相关论文
共 86 条
[1]  
Aggarwal BB, 2007, ADV EXP MED BIOL, V595, P1
[2]   Prospective identification of tumorigenic breast cancer cells [J].
Al-Hajj, M ;
Wicha, MS ;
Benito-Hernandez, A ;
Morrison, SJ ;
Clarke, MF .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2003, 100 (07) :3983-3988
[3]   Sensitization of neuroblastoma cells for TRAIL-induced apoptosis by NF-κB inhibition [J].
Ammann, Johannes U. ;
Haag, Christian ;
Kasperczyk, Hubert ;
Debatin, Klaus-Michael ;
Fulda, Simone .
INTERNATIONAL JOURNAL OF CANCER, 2009, 124 (06) :1301-1311
[4]   Cancer is a Preventable Disease that Requires Major Lifestyle Changes [J].
Anand, Preetha ;
Kunnumakara, Ajaikumar B. ;
Sundaram, Chitra ;
Harikumar, Kuzhuvelil B. ;
Tharakan, Sheeja T. ;
Lai, Oiki S. ;
Sung, Bokyung ;
Aggarwal, Bharat B. .
PHARMACEUTICAL RESEARCH, 2008, 25 (09) :2097-2116
[5]   Granulysin induces apoptotic cell death and cleavage of the autophagy regulator Atg5 in human hematological tumors [J].
Aporta, Adriana ;
Catalan, Elena ;
Galan-Malo, Patricia ;
Ramirez-Labrada, Ariel ;
Perez, Marta ;
Azaceta, Gemma ;
Palomera, Luis ;
Naval, Javier ;
Marzo, Isabel ;
Pardo, Julian ;
Anel, Alberto .
BIOCHEMICAL PHARMACOLOGY, 2014, 87 (03) :410-423
[6]  
Arceci R J, 1996, Curr Opin Hematol, V3, P279
[7]   A tale of two Paks [J].
Arias-Romero, Luis E. ;
Chernoff, Jonathan .
BIOLOGY OF THE CELL, 2008, 100 (02) :97-108
[8]   The regulation of self-renewal in human embryonic stem cells [J].
Avery, Stuart ;
Inniss, Katie ;
Moore, Harry .
STEM CELLS AND DEVELOPMENT, 2006, 15 (05) :729-740
[9]   PROTECTIVE ROLE OF AQUEOUS TURMERIC EXTRACT AGAINST MUTAGENICITY OF DIRECT-ACTING CARCINOGENS AS WELL AS BENZO[A]PYRENE-INDUCED GENOTOXICITY AND CARCINOGENICITY [J].
AZUINE, MA ;
KAYAL, JJ ;
BHIDE, SV .
JOURNAL OF CANCER RESEARCH AND CLINICAL ONCOLOGY, 1992, 118 (06) :447-452
[10]   p21-activated kinase-1 signaling mediates cyclin D1 expression in mammary epithelial and cancer cells [J].
Balasenthil, S ;
Sahin, AA ;
Barnes, CJ ;
Wang, RA ;
Pestell, RG ;
Vadlamudi, RK ;
Kumar, R .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2004, 279 (02) :1422-1428