• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

相似文献

1
Accelerated growth of intestinal tumours after radiation exposure in Mlh1-knockout mice: evaluation of the late effect of radiation on a mouse model of HNPCC.Mlh1基因敲除小鼠辐射暴露后肠道肿瘤的加速生长:对遗传性非息肉病性结直肠癌小鼠模型辐射晚期效应的评估
Int J Exp Pathol. 2006 Apr;87(2):89-99. doi: 10.1111/j.0959-9673.2006.00464.x.
2
Ionizing radiation, inflammation, and their interactions in colon carcinogenesis in Mlh1-deficient mice.电离辐射、炎症及其在Mlh1基因缺陷小鼠结肠癌发生中的相互作用
Cancer Sci. 2015 Mar;106(3):217-26. doi: 10.1111/cas.12591. Epub 2015 Feb 12.
3
Features of colorectal cancers with high-level microsatellite instability occurring in familial and sporadic settings: parallel pathways of tumorigenesis.家族性和散发性环境中发生的具有高度微卫星不稳定性的结直肠癌特征:肿瘤发生的平行途径
Am J Pathol. 2001 Dec;159(6):2107-16. doi: 10.1016/S0002-9440(10)63062-3.
4
Two types of sporadic multiple colorectal cancers with and without HNPCC-like genetic instability.两种具有和不具有HNPCC样基因不稳定的散发性多发性结直肠癌。
Hepatogastroenterology. 1999 Nov-Dec;46(30):3115-20.
5
Analysis of mismatch repair defects in the familial occurrence of lymphoma and colorectal cancer.
Leuk Lymphoma. 2002 Aug;43(8):1619-26. doi: 10.1080/1042819021000002956.
6
[The first molecular analysis of a Hungarian HNPCC family: a novel MSH2 germline mutation].[匈牙利一个遗传性非息肉病性结直肠癌家系的首次分子分析:一种新的错配修复基因MSH2种系突变]
Orv Hetil. 2005 May 15;146(20):1009-16.
7
Immunohistochemical pattern of MLH1/MSH2 expression is related to clinical and pathological features in colorectal adenocarcinomas with microsatellite instability.错配修复蛋白MLH1/MSH2表达的免疫组化模式与微卫星不稳定的结直肠癌的临床和病理特征相关。
Mod Pathol. 2002 Jul;15(7):741-9. doi: 10.1097/01.MP.0000018979.68686.B2.
8
Correlation of mismatch repair genes immunohistochemistry and microsatellite instability status in HNPCC-associated tumours.HNPCC相关肿瘤中错配修复基因免疫组化与微卫星不稳定性状态的相关性
Pathology. 2002 Dec;34(6):541-7. doi: 10.1080/0031302021000035965-2.
9
Association of colonic and endometrial carcinomas in Portuguese families with hereditary nonpolyposis colorectal carcinoma significantly increases the probability of detecting a pathogenic mutation in mismatch repair genes, primarily the MSH2 gene.葡萄牙家族中结肠直肠癌与子宫内膜癌的关联,伴遗传性非息肉病性结直肠癌,显著增加了在错配修复基因(主要是MSH2基因)中检测到致病突变的可能性。
Cancer. 2004 Jul 1;101(1):172-7. doi: 10.1002/cncr.20320.
10
Functional analysis of MLH1 mutations linked to hereditary nonpolyposis colon cancer.与遗传性非息肉病性结直肠癌相关的MLH1突变的功能分析。
Genes Chromosomes Cancer. 2002 Feb;33(2):160-7.

引用本文的文献

1
Ionizing Radiation May Induce Tumors Partly Through the Alteration or Regulation of Mismatch Repair Genes.电离辐射可能部分通过错配修复基因的改变或调控来诱发肿瘤。
Cancers (Basel). 2025 Feb 7;17(4):564. doi: 10.3390/cancers17040564.
2
Efficient prime editing in two-cell mouse embryos using PEmbryo.使用PEmbryo在双细胞小鼠胚胎中进行高效的碱基编辑。
Nat Biotechnol. 2024 Dec;42(12):1822-1830. doi: 10.1038/s41587-023-02106-x. Epub 2024 Feb 6.
3
Transgenerational Epigenetic DNA Methylation Editing and Human Disease.跨代表观遗传 DNA 甲基化编辑与人类疾病。
Biomolecules. 2023 Nov 22;13(12):1684. doi: 10.3390/biom13121684.
4
Moving the Needle Forward in Genomically-Guided Precision Radiation Treatment.推动基因组引导的精准放射治疗向前发展。
Cancers (Basel). 2023 Nov 7;15(22):5314. doi: 10.3390/cancers15225314.
5
Survival outcomes in locally advanced dMMR rectal cancer: surgery plus adjunctive treatment vs. surgery alone.局部晚期错配修复缺陷型直肠肿瘤的生存结局:手术联合辅助治疗与单纯手术的比较。
BMC Cancer. 2023 Oct 20;23(1):1013. doi: 10.1186/s12885-023-11525-7.
6
Engineering CpG island DNA methylation in pluripotent cells through synthetic CpG-free ssDNA insertion.通过合成不含 CpG 的 ssDNA 插入来实现多能干细胞中的 CpG 岛 DNA 甲基化工程化。
Cell Rep Methods. 2023 May 4;3(5):100465. doi: 10.1016/j.crmeth.2023.100465. eCollection 2023 May 22.
7
Interstitial deletion of the Apc locus in β-catenin-overexpressing cells is a signature of radiation-induced intestinal tumors in C3B6F1 ApcMin/+ mice†.β-连环蛋白过表达细胞中 APC 基因座的间质缺失是 C3B6F1 ApcMin/+ 小鼠辐射诱导肠道肿瘤的特征。
J Radiat Res. 2023 May 25;64(3):622-631. doi: 10.1093/jrr/rrad021.
8
Potential risks associated with the use of ionizing radiation for imaging and treatment of colorectal cancer in Lynch syndrome patients.林奇综合征患者中,用于结直肠癌成像和治疗的电离辐射的潜在风险。
Fam Cancer. 2023 Jan;22(1):61-70. doi: 10.1007/s10689-022-00299-9. Epub 2022 Jun 20.
9
Pharmacogenetic Review: Germline Genetic Variants Possessing Increased Cancer Risk With Clinically Actionable Therapeutic Relationships.药物遗传学综述:具有临床可操作治疗关系且癌症风险增加的种系基因变异
Front Genet. 2022 May 24;13:857120. doi: 10.3389/fgene.2022.857120. eCollection 2022.
10
Gene expression profiles of esophageal squamous cell cancers in Hodgkin lymphoma survivors versus sporadic cases.食管鳞癌在霍奇金淋巴瘤幸存者与散发性病例中的基因表达谱比较。
PLoS One. 2020 Dec 21;15(12):e0243178. doi: 10.1371/journal.pone.0243178. eCollection 2020.

本文引用的文献

1
Intestinal tumorigenesis in Min mice is enhanced by X-irradiation in an age-dependent manner.
J Radiat Res. 2005 Mar;46(1):83-91. doi: 10.1269/jrr.46.83.
2
Differential radiosensitization in DNA mismatch repair-proficient and -deficient human colon cancer xenografts with 5-iodo-2-pyrimidinone-2'-deoxyribose.5-碘-2-嘧啶酮-2'-脱氧核糖对DNA错配修复功能正常和缺陷的人结肠癌异种移植瘤的差异放射增敏作用
Clin Cancer Res. 2004 Nov 15;10(22):7520-8. doi: 10.1158/1078-0432.CCR-04-1144.
3
A panel of repeat markers for detection of microsatellite instability in murine tumors.用于检测小鼠肿瘤微卫星不稳定性的一组重复标记物。
Mol Carcinog. 2003 Dec;38(4):155-9. doi: 10.1002/mc.10157.
4
A role for DNA mismatch repair in sensing and responding to fluoropyrimidine damage.DNA错配修复在感知和应对氟嘧啶损伤中的作用。
Oncogene. 2003 Oct 20;22(47):7376-88. doi: 10.1038/sj.onc.1206941.
5
Multiple cutaneous and subcutaneous lesions occurring simultaneously with hereditary polyposis and osteomatosis.多发性皮肤和皮下病变与遗传性息肉病和骨瘤病同时出现。
Am J Hum Genet. 1953 Jun;5(2):139-47.
6
Pathogenesis of DNA repair-deficient cancers: a statistical meta-analysis of putative Real Common Target genes.DNA修复缺陷型癌症的发病机制:假定的真正共同靶基因的统计荟萃分析。
Oncogene. 2003 Apr 17;22(15):2226-35. doi: 10.1038/sj.onc.1206421.
7
The mammalian mismatch repair protein MSH2 is required for correct MRE11 and RAD51 relocalization and for efficient cell cycle arrest induced by ionizing radiation in G2 phase.哺乳动物错配修复蛋白MSH2是正确的MRE11和RAD51重新定位以及电离辐射诱导的G2期有效细胞周期停滞所必需的。
Oncogene. 2003 Apr 10;22(14):2110-20. doi: 10.1038/sj.onc.1206254.
8
Hereditary colorectal cancer.遗传性结直肠癌
N Engl J Med. 2003 Mar 6;348(10):919-32. doi: 10.1056/NEJMra012242.
9
Msh2 deficiency enhances somatic Apc and p53 mutations in Apc+/-Msh2-/- mice.Msh2基因缺陷增强了Apc+/-Msh2-/-小鼠的体细胞Apc和p53突变。
Carcinogenesis. 2003 Feb;24(2):217-24. doi: 10.1093/carcin/24.2.217.
10
The mismatch repair system is required for S-phase checkpoint activation.错配修复系统是S期检查点激活所必需的。
Nat Genet. 2003 Jan;33(1):80-4. doi: 10.1038/ng1052. Epub 2002 Nov 25.

Mlh1基因敲除小鼠辐射暴露后肠道肿瘤的加速生长:对遗传性非息肉病性结直肠癌小鼠模型辐射晚期效应的评估

Accelerated growth of intestinal tumours after radiation exposure in Mlh1-knockout mice: evaluation of the late effect of radiation on a mouse model of HNPCC.

作者信息

Tokairin Yutaka, Kakinuma Shizuko, Arai Masami, Nishimura Mayumi, Okamoto Mieko, Ito Eisaku, Akashi Makoto, Miki Yoshio, Kawano Tatsuyuki, Iwai Takehisa, Shimada Yoshiya

机构信息

Department of Surgery, Tokyo Medical and Dental University, 1-5-45 Yushima, Tokyo 113-8510, Japan.

出版信息

Int J Exp Pathol. 2006 Apr;87(2):89-99. doi: 10.1111/j.0959-9673.2006.00464.x.

DOI:10.1111/j.0959-9673.2006.00464.x
PMID:16623753
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2517356/
Abstract

Mlh1-knockout mice have been developed as a useful model of hereditary non-polyposis colorectal cancer (HNPCC). In this study, we analyzed the pathology of gastrointestinal tumours (GIT) in these mice in detail and examined the possible effects of ionizing radiation on the induction of intestinal tumours to evaluate the late response to radiotherapy in HNPCC. Mlh1-/- mice spontaneously developed GIT and thymic lymphomas by 48 weeks. GIT included not only well differentiated adenocarcinomas but also poorly differentiated and mucinous adenocarcinomas, suggesting that this mouse is a good model for HNPCC. In contrast to colon cancers from HNPCC patients, however, carcinomas of Mlh1-/- mice expressed p53 and showed a lack of transforming growth factor (TGF)-betaRII mutation, which resulted in the expression of TGF-betaRII protein. Irradiation of 10-week-old Mlh1-/- mice accelerated GIT development but had little effect at 2 weeks. Mlh1+/- and Mlh1+/+ mice were not susceptible to spontaneous or radiation-induced thymic lymphomas and GIT until 72 weeks after birth. The development and pathology of GIT in Mlh1-/- mice suggest that this mouse is a good model for HNPCC, although tumour-related responsible genes might be different from HNPCC. As X-ray exposure promoted carcinogenesis of GIT in adult Mlh1-/- mice, an increased risk of secondary cancers after radiotherapy for HNPCC patients should be taken into consideration.

摘要

Mlh1基因敲除小鼠已被培育成为遗传性非息肉病性结直肠癌(HNPCC)的有用模型。在本研究中,我们详细分析了这些小鼠胃肠道肿瘤(GIT)的病理学,并研究了电离辐射对肠道肿瘤诱导的可能影响,以评估HNPCC对放疗的晚期反应。Mlh1-/-小鼠在48周时自发发生GIT和胸腺淋巴瘤。GIT不仅包括高分化腺癌,还包括低分化和黏液腺癌,这表明该小鼠是HNPCC的良好模型。然而,与HNPCC患者的结肠癌不同,Mlh1-/-小鼠的癌表达p53,且缺乏转化生长因子(TGF)-βRII突变,这导致TGF-βRII蛋白的表达。对10周龄的Mlh1-/-小鼠进行照射可加速GIT的发展,但在2周时影响较小。Mlh1+/-和Mlh1+/+小鼠在出生后72周之前对自发或辐射诱导的胸腺淋巴瘤和GIT不敏感。Mlh1-/-小鼠GIT的发生和病理学表明,该小鼠是HNPCC的良好模型,尽管肿瘤相关的致病基因可能与HNPCC不同。由于X射线照射促进了成年Mlh1-/-小鼠GIT的致癌作用,因此应考虑HNPCC患者放疗后继发性癌症风险增加的问题。