TY - JOUR
T1 - A novel modification of the AOM/DSS model for inducing intestinal adenomas in mice
AU - Angelou, Anastasios
AU - Andreatos, Nikolaos
AU - Antoniou, Efstathios
AU - Zacharioudaki, Argiro
AU - Theodoropoulos, George
AU - Damaskos, Christos
AU - Garmpis, Nikolaos
AU - Yuan, Chunhui
AU - Xiao, Weidong
AU - Theocharis, Stamatios
AU - Zografos, George
AU - Papalois, Apostolos
AU - Margonis, Georgios Antonios
N1 - Publisher Copyright:
© 2018 International Institute of Anticancer Research. All rights reserved.
PY - 2018/6
Y1 - 2018/6
N2 - Background/Aim: Our aim was to develop an animal model of the precancerous stages of colitis-associated carcinogenesis by modifying the established azoxymethane/ dextran sulfate sodium (AOM/DSS) protocol. Materials and Methods: Six mice were treated with varying cycles of DSS following AOM administration as above (group 1: three mice received three 5-day cycles of 3.0% DSS and group 2: three mice received three 7-day cycles of 2.5% DSS; every cycle was followed by a 2-week rest period) and were sacrificed on day 84 of the experiment. By contrast, three female C57BL6 mice (group 3) were treated with a single intraperitoneal dose (10 mg/kg of body weight) of AOM followed by three 5-day cycles of oral 2.5% DSS, with each cycle interrupted by a 2-week rest period. The mice of this group were sacrificed at 60 days. Results: In groups 1 and 2, cancer was noted in five out of the six mice. In group 3, adenomas with dysplastic lesions were noted in all of the mice, but none had developed adenocarcinoma. Conclusion: Our results suggest that the administration of three 5-day cycles of 2.5% DSS following an initial dose of AOM may successfully induce adenoma formation without the concurrent presence of carcinoma in female C57BL6 mice that are sacrificed on experimental day 60. In turn, this modification of the widely used AOM/DSS protocol may constitute a novel approach for investigating colitis-related colonic adenomas.
AB - Background/Aim: Our aim was to develop an animal model of the precancerous stages of colitis-associated carcinogenesis by modifying the established azoxymethane/ dextran sulfate sodium (AOM/DSS) protocol. Materials and Methods: Six mice were treated with varying cycles of DSS following AOM administration as above (group 1: three mice received three 5-day cycles of 3.0% DSS and group 2: three mice received three 7-day cycles of 2.5% DSS; every cycle was followed by a 2-week rest period) and were sacrificed on day 84 of the experiment. By contrast, three female C57BL6 mice (group 3) were treated with a single intraperitoneal dose (10 mg/kg of body weight) of AOM followed by three 5-day cycles of oral 2.5% DSS, with each cycle interrupted by a 2-week rest period. The mice of this group were sacrificed at 60 days. Results: In groups 1 and 2, cancer was noted in five out of the six mice. In group 3, adenomas with dysplastic lesions were noted in all of the mice, but none had developed adenocarcinoma. Conclusion: Our results suggest that the administration of three 5-day cycles of 2.5% DSS following an initial dose of AOM may successfully induce adenoma formation without the concurrent presence of carcinoma in female C57BL6 mice that are sacrificed on experimental day 60. In turn, this modification of the widely used AOM/DSS protocol may constitute a novel approach for investigating colitis-related colonic adenomas.
KW - Adenomas
KW - Animal model
KW - AOM/DSS
KW - IBD
UR - http://www.scopus.com/inward/record.url?scp=85048227033&partnerID=8YFLogxK
U2 - 10.21873/anticanres.12616
DO - 10.21873/anticanres.12616
M3 - Article
C2 - 29848698
AN - SCOPUS:85048227033
SN - 0250-7005
VL - 38
SP - 3467
EP - 3470
JO - Anticancer research
JF - Anticancer research
IS - 6
ER -