TY - JOUR
T1 - A comprehensive evaluation of an animal model for Helicobacter pylori-associated stomach cancer
T2 - Fact and controversy
AU - Amalia, Rizki
AU - Panenggak, Nur Syahadati Retno
AU - Doohan, Dalla
AU - Rezkitha, Yudith Annisa Ayu
AU - Waskito, Langgeng Agung
AU - Syam, Ari Fahrial
AU - Lubis, Masrul
AU - Yamaoka, Yoshio
AU - Miftahussurur, Muhammad
N1 - Publisher Copyright:
© 2023 John Wiley & Sons Ltd.
PY - 2023/2
Y1 - 2023/2
N2 - Even though Helicobacter pylori infection was the most causative factor of gastric cancer, numerous in vivo studies failed to induce gastric cancer using H. pylori infection only. The utilization of established animal studies in cancer research is crucial as they aim to investigate the coincidental association between suspected oncogenes and pathogenesis as well as generate models for the development and testing of potential treatments. The methods to establish gastric cancer using infected animal models remain limited, diverse in methods, and showed different results. This study investigates the differences in animal models, which highlight different pathological results in gaster by literature research. Electronic databases searched were performed in PubMed, Science Direct, and Cochrane, without a period filter. A total of 135 articles were used in this study after a full-text assessment was conducted. The most frequent animal models used for gastric cancer were Mice, while Mongolian gerbils and Transgenic mice were the most susceptible model for gastric cancer associated with H. pylori infection. Additionally, transgenic mice showed that the susceptibility to gastric cancer progression was due to genetic and epigenetic factors. These studies showed that in Mongolian gerbil models, H. pylori could function as a single agent to trigger stomach cancer. However, most gastric cancer susceptibilities were not solely relying on H. pylori infection, and numerous factors are involved in cancer progression. Further study using Mongolian gerbils and Transgenic mice is crucial to conduct and establish the best models for gastric cancer associated H. pylori.
AB - Even though Helicobacter pylori infection was the most causative factor of gastric cancer, numerous in vivo studies failed to induce gastric cancer using H. pylori infection only. The utilization of established animal studies in cancer research is crucial as they aim to investigate the coincidental association between suspected oncogenes and pathogenesis as well as generate models for the development and testing of potential treatments. The methods to establish gastric cancer using infected animal models remain limited, diverse in methods, and showed different results. This study investigates the differences in animal models, which highlight different pathological results in gaster by literature research. Electronic databases searched were performed in PubMed, Science Direct, and Cochrane, without a period filter. A total of 135 articles were used in this study after a full-text assessment was conducted. The most frequent animal models used for gastric cancer were Mice, while Mongolian gerbils and Transgenic mice were the most susceptible model for gastric cancer associated with H. pylori infection. Additionally, transgenic mice showed that the susceptibility to gastric cancer progression was due to genetic and epigenetic factors. These studies showed that in Mongolian gerbil models, H. pylori could function as a single agent to trigger stomach cancer. However, most gastric cancer susceptibilities were not solely relying on H. pylori infection, and numerous factors are involved in cancer progression. Further study using Mongolian gerbils and Transgenic mice is crucial to conduct and establish the best models for gastric cancer associated H. pylori.
KW - animal model
KW - cancer
KW - gastric cancer
KW - Helicobacter pylori
UR - http://www.scopus.com/inward/record.url?scp=85146173960&partnerID=8YFLogxK
U2 - 10.1111/hel.12943
DO - 10.1111/hel.12943
M3 - Review article
C2 - 36627714
AN - SCOPUS:85146173960
SN - 1083-4389
VL - 28
JO - Helicobacter
JF - Helicobacter
IS - 1
M1 - e12943
ER -