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来自十二项美国国家毒理学计划两年致癌性研究的B6C3F1小鼠感染肝螺杆菌的影响。

Impact of Helicobacter hepaticus infection in B6C3F1 mice from twelve National Toxicology Program two-year carcinogenesis studies.

作者信息

Hailey J R, Haseman J K, Bucher J R, Radovsky A E, Malarkey D E, Miller R T, Nyska A, Maronpot R R

机构信息

National Toxicology Program, National Institute of Environmental Health Sciences, Research Triangle Park, North Carolina 27709, USA.

出版信息

Toxicol Pathol. 1998 Sep-Oct;26(5):602-11. doi: 10.1177/019262339802600503.

Abstract

Male and female B6C3F1 mice from 12 National Toxicology Program (NTP) 2-yr carcinogenesis studies were found to be infected with Helicobacter hepaticus. Many of the male mice from 9 of these studies had an associated hepatitis (affected studies). Helicobacter hepaticus has been reported to be associated with an increased incidence of hepatitis and hepatocellular neoplasms in the A/JCr male mouse. We attempted to determine if the data from the Helicobacter-affected NTP B6C3F1 mouse studies were compromised and unsuitable for cancer hazard identification. The incidences of neoplasms of the liver (both hepatocellular and hemangiosarcoma) but not of other organs in control male B6C3F1 mice were increased in affected studies as compared with control males from unaffected studies. The increased incidence of hepatocellular neoplasms was observed in those males exhibiting H. hepaticus-associated hepatitis. Other observations further differentiated control male mice from affected and unaffected studies. H-ras codon 61 CAA to AAA mutations were less common in liver neoplasms from males from affected studies as compared with historical and study controls. In addition, increases in cell proliferation rates and apoptosis were observed in the livers of male mice with H. hepaticus-associated hepatitis. These data support the hypothesis that the increased incidence of liver neoplasms is associated with H. hepaticus and that hepatitis may be important in the pathogenesis. Therefore, interpretation of carcinogenic effects in the liver of B6C3F1 mice may be confounded if there is H. hepaticus-associated hepatitis.

摘要

在12项美国国家毒理学计划(NTP)的2年致癌性研究中,发现雄性和雌性B6C3F1小鼠感染了肝螺杆菌。其中9项研究中的许多雄性小鼠伴有肝炎(受影响的研究)。据报道,肝螺杆菌与A/JCr雄性小鼠肝炎和肝细胞肿瘤发病率增加有关。我们试图确定受肝螺杆菌影响的NTP B6C3F1小鼠研究数据是否受到影响且不适用于癌症风险识别。与未受影响研究中的对照雄性小鼠相比,受影响研究中对照雄性B6C3F1小鼠的肝脏肿瘤(肝细胞肿瘤和血管肉瘤)而非其他器官肿瘤的发病率有所增加。在表现出与肝螺杆菌相关肝炎的雄性小鼠中观察到肝细胞肿瘤发病率增加。其他观察结果进一步区分了受影响和未受影响研究中的对照雄性小鼠。与历史对照和研究对照相比,受影响研究中雄性小鼠肝脏肿瘤中H-ras密码子61由CAA突变为AAA的情况较少见。此外,在患有与肝螺杆菌相关肝炎的雄性小鼠肝脏中观察到细胞增殖率和细胞凋亡增加。这些数据支持了肝脏肿瘤发病率增加与肝螺杆菌有关且肝炎可能在发病机制中起重要作用这一假设。因此,如果存在与肝螺杆菌相关的肝炎,对B6C3F1小鼠肝脏致癌作用的解释可能会受到混淆。

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