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低剂量替匹法尼对缺氧诱导因子-1α表达的胃癌细胞中 mTOR 信号通路和活性氧产生的抗肿瘤作用。

Antitumor effects of low-dose tipifarnib on the mTOR signaling pathway and reactive oxygen species production in HIF-1α-expressing gastric cancer cells.

机构信息

Department of Surgery, Saga University Faculty of Medicine, Japan.

Department of Surgery, National Hospital Organization Higashisaga Hospital, Saga, Japan.

出版信息

FEBS Open Bio. 2021 May;11(5):1465-1475. doi: 10.1002/2211-5463.13154. Epub 2021 Apr 8.

Abstract

Farnesyltransferase inhibitors (FTIs) suppress tumor aggressiveness in several malignancies by inhibiting Ras signaling. However, treatment of cells with a low dose of the FTI tipifarnib suppresses the expression of hypoxia-inducible factor-1α (HIF-1α) and results in antitumor effects without inhibiting the Ras pathway. Although we previously reported that elevated HIF-1α expression is associated with an aggressive phenotype in gastric cancer (GC), little is known about the antitumor effects of FTIs on GC. In this study, we examined the relationship between the antitumor effects of low-dose tipifarnib and HIF-1α expression in GC cells. Under normoxic conditions, HIF-1α was expressed only in MKN45 and KATOIII cells. The inhibitory effect of tipifarnib on HIF-1α was observed in HIF-1α-positive cells. Low-dose tipifarnib had antitumor effects only on HIF-1α-positive cells both in vitro and in vivo. Furthermore, low-dose tipifarnib inactivated ras homolog enriched in brain (Rheb)/mammalian target of rapamycin (mTOR) signaling and decreased intracellular reactive oxygen species (ROS) levels in HIF-1α-positive GC cells. Our results that the antitumor effects of low-dose tipifarnib are at least partially mediated through suppression of mTOR signaling and HIF-1α expression via inhibition of Rheb farnesylation and reduction in ROS levels. These findings suggest that low-dose tipifarnib may be capable of exerting an antitumor effect that is dependent on HIF-1α expression in GC cells. Tipifarnib may have potential as a novel therapeutic agent for HIF-1α-expressing GC exhibiting an aggressive phenotype.

摘要

法呢基转移酶抑制剂(FTIs)通过抑制 Ras 信号抑制多种恶性肿瘤的肿瘤侵袭性。然而,用低剂量的 FTI 替吡法尼治疗细胞会抑制低氧诱导因子-1α(HIF-1α)的表达,并在不抑制 Ras 途径的情况下产生抗肿瘤作用。虽然我们之前报道过,在胃癌(GC)中,HIF-1α的表达升高与侵袭性表型有关,但对于 FTI 对 GC 的抗肿瘤作用知之甚少。在这项研究中,我们研究了低剂量替吡法尼的抗肿瘤作用与 GC 细胞中 HIF-1α表达之间的关系。在常氧条件下,只有在 MKN45 和 KATOIII 细胞中表达 HIF-1α。在 HIF-1α阳性细胞中观察到替吡法尼对 HIF-1α的抑制作用。低剂量替吡法尼仅对 HIF-1α阳性细胞具有抗肿瘤作用,无论是在体外还是体内。此外,低剂量替吡法尼在 HIF-1α阳性 GC 细胞中可使 Ras 同源物富含脑(Rheb)/雷帕霉素(mTOR)信号失活,并降低细胞内活性氧(ROS)水平。我们的结果表明,低剂量替吡法尼的抗肿瘤作用至少部分是通过抑制 Rheb 法尼基化和降低 ROS 水平来抑制 mTOR 信号和 HIF-1α表达介导的。这些发现表明,低剂量替吡法尼可能能够在表达 HIF-1α的 GC 细胞中发挥抗肿瘤作用,该作用依赖于 HIF-1α的表达。替吡法尼可能有潜力成为表达侵袭性表型的 HIF-1α 的 GC 的新型治疗剂。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e403/8091580/12d8271ffacc/FEB4-11-1465-g006.jpg

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