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[缺氧微环境与癌症休眠]

[Hypoxic microenvironment and cancer dormancy].

作者信息

Okuyama Hiroaki, Inoue Masahiro

机构信息

Department of Biochemistry, Osaka Medical Center for Cancer and Cardiovascular Diseases, Osaka, Japan.

出版信息

Gan To Kagaku Ryoho. 2011 Oct;38(10):1559-64.

Abstract

The microenvironment of solid tumors is heterogeneous, and hypoxia is associated with the malignancy of cancers. In this review, we introduce the characteristics of cancer cells in hypoxic areas. The hypoxic response of cancer cells in vivo is different from that in vitro. The expression of MYC is downregulated in the cancer cells in hypoxic regions. Cancer cell proliferation and its metabolism are dramatically suppressed in the hypoxic area, and are in a stage of cellular dormancy. Dual deficiency of oxygen and glucose in vitro induces dormancy of cancer cells in hypoxic regions. Researchers have focused on the proliferation of cancer cells so far, but aside from proliferation, it is important for the survival of cancer cells that they become inactive/ dormant in the hypoxic regions. Dormant cancer cells become resistant to chemotherapy and irradiation, leading to recurrence and metastasis. Therefore, we need to characterize and target dormant cancer cells in the hypoxic regions.

摘要

实体瘤的微环境是异质性的,缺氧与癌症的恶性程度相关。在本综述中,我们介绍缺氧区域癌细胞的特征。体内癌细胞的缺氧反应与体外不同。缺氧区域癌细胞中MYC的表达下调。缺氧区域癌细胞的增殖及其代谢受到显著抑制,处于细胞休眠阶段。体外氧和葡萄糖的双重缺乏诱导缺氧区域癌细胞的休眠。到目前为止,研究人员一直专注于癌细胞的增殖,但除了增殖之外,癌细胞在缺氧区域进入静止/休眠状态对其存活也很重要。休眠癌细胞对化疗和放疗产生抗性,导致复发和转移。因此,我们需要对缺氧区域的休眠癌细胞进行表征并将其作为靶点。

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