Low molecular weight hyaluronan inhibits colorectal carcinoma growth by decreasing tumor cell proliferation and stimulating immune response

被引:53
作者
Alaniz, Laura [1 ,2 ]
Rizzo, Miguel [1 ]
Malvicini, Mariana [1 ]
Jaunarena, Jorge [1 ]
Avella, Diego [1 ]
Atorrasagasti, Catalina [1 ]
Aquino, Jorge B. [1 ]
Garcia, Mariana [1 ,2 ,3 ]
Matar, Pablo [2 ,4 ]
Silva, Marcelo [1 ]
Mazzolini, Guilermo [1 ,2 ]
机构
[1] Austral Univ, Sch Med, Liver Unit, Buenos Aires, DF, Argentina
[2] Consejo Nacl Invest Cient & Tecn, RA-1033 Buenos Aires, DF, Argentina
[3] Univ Buenos Aires, Fac Farm & Bioquim, Catedra Inmunol, IDEHU CONICET, RA-1113 Buenos Aires, DF, Argentina
[4] Univ Nacl Rosario, Fac Ciencias Med, Inst Genet Expt, RA-2900 Rosario, Santa Fe, Argentina
关键词
Hyaluronan; Colorectal carcinoma; Dendritic cells; MHC class II; TISSUE-INJURY; T-CELLS; IN-VIVO; OLIGOSACCHARIDES; LINES; CD44; MACROPHAGES; EXPRESSION; PROMOTES; DEATH;
D O I
10.1016/j.canlet.2008.12.029
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
Hyaluronan modulates cancer progression by multiple mechanisms: nevertheless, its effects remain controversial. In this work, low molecular weight (LMW) hyaluronan but not high molecular weight (HMW) was found to significantly reduce colorectal carcinoma (CRC) growth in vitro and in vivo. Both survival and proliferation of CT26 tumor cells were affected by treatment with low doses of LMW HA, with involvement of Akt signaling mechanisms. We show for the first time that splenocytes isolated from LMW HA-treated animals present significantly higher proliferative capacity upon stimulation with dendritic cells (DCs) pulsed with tumor lysate. Consistently, expression of MHC class II and costimulatory molecules were increased in DCs isolated from the spleen of LMW HA-treated mice. Besides, increased tumor infiltrating lymphocytes was observed in animals treated with LMW HA. Our results suggest that LMW HA in a model of CRC triggers an activation of immune system, which is likely involved in the observed tumor growth inhibition. LMW HA is suggested as a candidate molecule for therapeutic adjuvant treatments in CRC immunotherapy. (c) 2008 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:9 / 16
页数:8
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