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探究溃疡性结肠炎、结直肠癌和前列腺癌之间的关系。

Exploring the relationship between ulcerative colitis, colorectal cancer, and prostate cancer.

作者信息

Kura Yurie, De Velasco Marco A, Sakai Kazuko, Uemura Hirotsugu, Fujita Kazutoshi, Nishio Kazuto

机构信息

Department of Genome Biology, Faculty of Medicine, Kindai University, 377-2 Ohno-Higashi, Osaka-Sayama, Osaka, 589-8511, Japan.

Department of Urology, Faculty of Medicine, Kindai University, 377-2 Ohno-Hiashi, Osaka-Sayama, Osaka, 589-8511, Japan.

出版信息

Hum Cell. 2024 Nov;37(6):1706-1718. doi: 10.1007/s13577-024-01118-2. Epub 2024 Aug 20.

Abstract

Chronic systemic inflammation caused by diseases such as ulcerative colitis (UC) and Crohn's disease (CD) increases the risk of developing colorectal cancer (CRC). Recent evidence indicates that patients with UC are more susceptible to prostate cancer (PCa), and individuals with PCa may also be at a higher risk of developing CRC. However, these relationships are not well defined. A better understanding of this phenomenon could improve the identification of high-risk populations. In this study, we characterized these relationships with experiments using preclinical mouse models of dextran sulfate sodium (DSS)-induced colitis (DSS-UC) and DSS/azoxymethane (AOM)-induced CRC (DSS/AOM-CRC) in wild-type and conditional transgenic mice of PCa. We showed that DSS-induced UC was more severe in mice with PCa and resulted in the development of CRC in the absence of AOM. We further showed that PCa-free mice that developed DSS-induced UC also showed histological changes in the normal prostate that resembled proliferative inflammatory atrophy. Finally, we used immunohistochemical immune profiling to show that mice with PCa-induced chronic systemic inflammation accumulated Gr1 myeloid cells in the normal colon and exposure to DSS further enriched these cells in active colitis regions and colon tumors. Our study provides evidence to support a link between systemic chronic inflammation and cancer.

摘要

由溃疡性结肠炎(UC)和克罗恩病(CD)等疾病引起的慢性全身性炎症会增加患结直肠癌(CRC)的风险。最近的证据表明,UC患者更容易患前列腺癌(PCa),而PCa患者患CRC的风险可能也更高。然而,这些关系尚未明确界定。更好地理解这一现象有助于改善高危人群的识别。在本研究中,我们利用葡聚糖硫酸钠(DSS)诱导的结肠炎(DSS-UC)和DSS/氧化偶氮甲烷(AOM)诱导的CRC(DSS/AOM-CRC)的临床前小鼠模型,在野生型和条件性转基因PCa小鼠中通过实验对这些关系进行了表征。我们发现,DSS诱导的UC在PCa小鼠中更为严重,并且在没有AOM的情况下会导致CRC的发生。我们进一步发现,发生DSS诱导的UC的无PCa小鼠在正常前列腺中也表现出类似于增殖性炎性萎缩的组织学变化。最后,我们通过免疫组织化学免疫分析表明,PCa诱导的慢性全身性炎症小鼠在正常结肠中积累了Gr1髓样细胞,而暴露于DSS会使这些细胞在活动性结肠炎区域和结肠肿瘤中进一步富集。我们的研究为支持全身性慢性炎症与癌症之间的联系提供了证据。

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