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细胞应激通过激活热休克因子1来诱导DNAJB8的表达,从而产生癌症干细胞样细胞。

Cellular stress induces cancer stem-like cells through expression of DNAJB8 by activation of heat shock factor 1.

作者信息

Kusumoto Hiroki, Hirohashi Yoshihiko, Nishizawa Satoshi, Yamashita Masamichi, Yasuda Kazuyo, Murai Aiko, Takaya Akari, Mori Takashi, Kubo Terufumi, Nakatsugawa Munehide, Kanaseki Takayuki, Tsukahara Tomohide, Kondo Toru, Sato Noriyuki, Hara Isao, Torigoe Toshihiko

机构信息

Department of Pathology, Sapporo Medical University School of Medicine, Sapporo, Japan.

Department of Urology, Wakayama Medical University, Wakayama, Japan.

出版信息

Cancer Sci. 2018 Mar;109(3):741-750. doi: 10.1111/cas.13501. Epub 2018 Feb 20.

Abstract

In a previous study, we found that DNAJB8, a heat shock protein (HSP) 40 family member is expressed in kidney cancer stem-like cells (CSC)/cancer-initiating cells (CIC) and that it has a role in the maintenance of kidney CSC/CIC. Heat shock factor (HSF) 1 is a key transcription factor for responses to stress including heat shock, and it induces HSP family expression through activation by phosphorylation. In the present study, we therefore examined whether heat shock (HS) induces CSC/CIC. We treated the human kidney cancer cell line ACHN with HS, and found that HS increased side population (SP) cells. Western blot analysis and qRT-PCR showed that HS increased the expression of DNAJB8 and SOX2. Gene knockdown experiments using siRNAs showed that the increase in SOX2 expression and SP cell ratio depends on DNAJB8 and that the increase in DNAJB8 and SOX2 depend on HSF1. Furthermore, treatment with a mammalian target of rapamycin (mTOR) inhibitor, temsirolimus, decreased the expression of DNAJB8 and SOX2 and the ratio of SP cells. Taken together, the results indicate that heat shock induces DNAJB8 by activation of HSF1 and induces cancer stem-like cells.

摘要

在先前的一项研究中,我们发现DNAJB8,一种热休克蛋白(HSP)40家族成员,在肾癌干细胞样细胞(CSC)/癌症起始细胞(CIC)中表达,并且它在维持肾CSC/CIC方面发挥作用。热休克因子(HSF)1是对应激(包括热休克)反应的关键转录因子,它通过磷酸化激活来诱导HSP家族的表达。因此,在本研究中,我们检测了热休克(HS)是否诱导CSC/CIC。我们用HS处理人肾癌细胞系ACHN,发现HS增加了侧群(SP)细胞。蛋白质印迹分析和qRT-PCR表明,HS增加了DNAJB8和SOX2的表达。使用小干扰RNA(siRNA)进行的基因敲低实验表明,SOX2表达和SP细胞比例的增加依赖于DNAJB8,而DNAJB8和SOX2的增加依赖于HSF1。此外,用雷帕霉素靶蛋白(mTOR)抑制剂替西罗莫司处理可降低DNAJB8和SOX2的表达以及SP细胞的比例。综上所述,结果表明热休克通过激活HSF1诱导DNAJB8并诱导癌症干细胞样细胞。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/da71/5834799/f0de7fac2b02/CAS-109-741-g001.jpg

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