Prophylactic effects of secretion metabolites of dairy lactobacilli through downregulation of ErbB-2 and ErbB-3 genes on colon cancer cells

被引:18
|
作者
Faghfoori, Zeinab [1 ,2 ]
Gargari, Bahram Pourghassem [3 ,4 ]
Saber, Amir [3 ,4 ]
Seyyedi, Maryam [2 ]
Fazelian, Siavash [7 ]
Khosroushahi, Ahmad Yari [5 ,6 ]
机构
[1] Semnan Univ Med Sci, Food Salt Safety Res Ctr, Semnan, Iran
[2] Tabriz Univ Med Sci, TB & Lung Res Ctr, Tabriz, Iran
[3] Tabriz Univ Med Sci, Biotechnol Res Ctr, Tabriz, Iran
[4] Tabriz Univ Med Sci, Dept Biochem & Diet Therapy, Nutr Res Ctr, Fac Nutr, Tabriz, Iran
[5] Tabriz Univ Med Sci, Drug Appl Res Ctr, Tabriz, Iran
[6] Tabriz Univ Med Sci, Dept Pharmacognosy, Fac Pharm, POB 51664-14766,Daneshgah St, Tabriz 5355155646, Iran
[7] Isfahan Univ Med Sci, Food Secur Res Ctr, Sch Nutr & Food Sci, Dept Clin Nutr, Esfahan, Iran
关键词
colorectal cancer; gene expression; probiotics; traditional dairy products; LACTIC-ACID BACTERIA; COLORECTAL-CANCER; TYROSINE KINASE; PROBIOTICS; FAMILY; OVEREXPRESSION; CARCINOGENESIS; PREBIOTICS; MICROBIOTA; LIFE;
D O I
10.1097/CEJ.0000000000000393
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Colon cancer is one of the most prevalent cancers, and intestinal microbial community plays a pivotal role in colorectal tumor genesis. Probiotics as live microorganisms may be able to exert an anticancer effect in colon cancer. The aim of this study was to isolate and identify Lactobacillus spp. from traditional dairy products with probiotic properties and to investigate their anticancer effects through ErbB-2 and ErbB-3 gene expression in colon cancer cells. The isolated lactobacilli from yogurt and cheese samples were molecularly identified by blasting of 16-23s rDNA region PCR sequenced products. The probiotic properties, including acid and bile tolerance, antimicrobial activity, and antibiotic susceptibility, were assayed. The proliferation inhibition effects of lactobacilli secretion metabolites with probiotic potential on colon cancer cell lines (HT-29 and caco-2) were analyzed using MTT assay. The real-time PCR was used for assessment of ErbB-2 and ErbB-3 gene expression after being treated with probiotics. Four species of bacteria with the most probiotic properties, including Lactobacillus casei, Lactobacillus paracasei, Lactobacillus rhamnosus, and Lactobacillus plantarum, were characterized and their effects on different human cell lines were taken into consideration. Total bacterial secretions significantly reduced the viability of HT-29 and caco-2 cancer cells compared with untreated controls. The metabolites secreted by bacteria downregulated the expression of ErbB-2 and ErbB-3 genes in colon cancer cells. The present study indicated that probiotic bacteria isolated from traditional dairy products exert anticancer effect on colon cancer cells through the downregulation of ErbB-2 and ErbB-3 gene expression.
引用
收藏
页码:201 / 209
页数:9
相关论文
共 50 条
  • [31] Tanshinone IIA down-regulates the protein expression of ErbB-2 and up-regulates TNF-α in colon cancer cells in vitro and in vivo
    Su, Chin-Cheng
    Lin, Yi-Hsiang
    INTERNATIONAL JOURNAL OF MOLECULAR MEDICINE, 2008, 22 (06) : 847 - 851
  • [32] ErbB-3 activation by NRG-1β sustains growth and promotes vemurafenib resistance in BRAF-V600E colon cancer stem cells (CSCs)
    Prasetyanti, Pramudita R.
    Capone, Emily
    Barcaroli, Daniela
    D'Agostino, Daniela
    Volpe, Silvia
    Benfante, Antonina
    van Hooff, Sander
    Iacobelli, Valentina
    Rossi, Cosmo
    Iacobelli, Stefano
    Medema, Jan Paul
    De laurenzi, Vincenzo
    Sala, Gianluca
    ONCOTARGET, 2015, 6 (19) : 16902 - 16911
  • [33] Effects of the combined blockade of EGFR and ErbB-2 on signal transduction and regulation of cell cycle regulatory proteins in breast cancer cells.
    D'Alessio, A.
    De Luca, A.
    Maiello, M. R.
    Palumbo, C.
    Rachiglio, A. M.
    Gallo, M.
    Normanno, N.
    CANCER RESEARCH, 2009, 69 (02) : 195S - 195S
  • [34] Aberrant expression of proteinase-activated receptor 4 promotes colon cancer cell proliferation through a persistent signaling that involves Src and ErbB-2 kinase
    Gratio, Valerie
    Walker, Francine
    Lehy, Therese
    Laburthe, Marc
    Darmoul, Dalila
    INTERNATIONAL JOURNAL OF CANCER, 2009, 124 (07) : 1517 - 1525
  • [35] ON-III inhibits erbB-2 tyrosine kinase receptor signal pathway and triggers apoptosis through induction of Bim in breast cancer cells
    Li, Dan-Dan
    Wu, Xiao-Qi
    Tang, Jun
    Wei, Xiao-Yi
    Zhu, Xiao-Feng
    CANCER BIOLOGY & THERAPY, 2009, 8 (08) : 739 - 743
  • [36] Activation of Stat3 by Heregulin/ErbB-2 through the Co-Option of Progesterone Receptor Signaling Drives Breast Cancer Growth
    Proietti, Cecilia J.
    Rosemblit, Cinthia
    Beguelin, Wendy
    Rivas, Martin A.
    Diaz Flaque, Maria Celeste
    Charreau, Eduardo H.
    Schillaci, Roxana
    Elizalde, Patricia V.
    MOLECULAR AND CELLULAR BIOLOGY, 2009, 29 (05) : 1249 - 1265
  • [37] Engagement of immune effector cells by trastuzumab induces HER2/ERBB2 downregulation in cancer cells through STAT1 activation
    Shi, Yun
    Fan, Xuejun
    Meng, Weixu
    Deng, Hui
    Zhang, Ningyan
    An, Zhiqiang
    BREAST CANCER RESEARCH, 2014, 16 (02)
  • [38] Engagement of immune effector cells by trastuzumab induces HER2/ERBB2 downregulation in cancer cells through STAT1 activation
    Yun Shi
    Xuejun Fan
    Weixu Meng
    Hui Deng
    Ningyan Zhang
    Zhiqiang An
    Breast Cancer Research, 16
  • [39] Optical imaging detection of microscopic mammary cancer in ErbB-2 transgenic mice through the DA364 probe binding v3 integrins
    Conti, Laura
    Lanzardo, Stefania
    Iezzi, Manuela
    Montone, Monica
    Bolli, Elisabetta
    Brioschi, Chiara
    Maiocchi, Alessandro
    Forni, Guido
    Cavallo, Federica
    CONTRAST MEDIA & MOLECULAR IMAGING, 2013, 8 (04) : 350 - 360
  • [40] Functional cooperation of miR-125a, miR-125b, and miR-205 in entinostat-induced downregulation of erbB2/erbB3 and apoptosis in breast cancer cells
    S Wang
    J Huang
    H Lyu
    C-K Lee
    J Tan
    J Wang
    B Liu
    Cell Death & Disease, 2013, 4 : e556 - e556