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在恶性嗜铬细胞瘤的治疗中,靶向mTORC2可能比选择性靶向mTORC1具有优势。

Targeting of mTORC2 may have advantages over selective targeting of mTORC1 in the treatment of malignant pheochromocytoma.

作者信息

Zhang Xiaohua, Wang Xianjin, Xu Tianyuan, Zhong Shan, Shen Zhoujun

机构信息

Department of Urology, Ruijin Hospital, Shanghai Jiaotong University School of Medicine, Shanghai, 200025, China.

出版信息

Tumour Biol. 2015 Jul;36(7):5273-81. doi: 10.1007/s13277-015-3187-7. Epub 2015 Feb 11.

Abstract

Recent studies have found that mammalian target of rapamycin complex 2 (mTORC2) is emerging as a potential therapeutic target in the treatment of many human cancers. However, the effects of targeting of mTORC2 on malignant pheochromocytomas (PCC) and paragangliomas (PGL) have not been reported. The aim of the study was to investigate the effects of targeting of mTORC2 on malignant PCC/PGL by comparing the inhibitory effects of targeting of mTORC2 with mTORC1 on pheochromocytoma PC12 cell in vitro and vivo. The expressions of regulatory-associated protein of mTOR (raptor) and rapamycin-insensitive companion of mTOR (rictor) were detected by immunohistochemistry in human tissues of malignant PCC. Targeting of mTORC1, mTORC2, and mTORC1/2 (mTORC1 and mTORC2) were performed by transfected with raptor, rictor, and mammalian target of rapamycin (mTOR) small interfering RNA (siRNA) in pheochromocytoma PC12 cell, respectively. MTT assay, apoptosis analysis, wound healing, and Transwell approach were performed. A tumor model in nude mice bearing PC12 cell xenografts, which were dosed with rapamycin or PP242, was established. The expression of raptor was frequently moderate positive, but the expression of rictor was frequently strong positive in malignant PCC. In vitro, although inhibition of mTORC1 was able to suppress PC12 cell proliferation, inhibition of mTORC2 more effectively suppressed cell proliferation. Inhibition of mTORC2 or mTORC1/2 more effectively prevented cell migration and invasion, and promoted cell apoptosis, while inhibition of mTORC1 only slightly prevented cell migration and invasion, and was not able to promoted apoptosis. Also, we found that mTOR downstream kinases were deregulated by targeting of mTORC2, but not mTORC1. In vivo, we found that PP242 was more potent than rapamycin in inhibiting tumor growth in tumor model. Our data suggest that targeting of mTORC2 may have advantages over selective targeting of mTORC1 in the treatment of malignant PCC/PGL. However, more clinical trials are needed to prove our findings.

摘要

近期研究发现,雷帕霉素靶蛋白复合物2(mTORC2)正成为治疗多种人类癌症的潜在治疗靶点。然而,靶向mTORC2对恶性嗜铬细胞瘤(PCC)和副神经节瘤(PGL)的影响尚未见报道。本研究的目的是通过比较靶向mTORC2与mTORC1在体外和体内对嗜铬细胞瘤PC12细胞的抑制作用,来研究靶向mTORC2对恶性PCC/PGL的影响。通过免疫组织化学检测恶性PCC人体组织中mTOR调节相关蛋白(raptor)和mTOR雷帕霉素不敏感伴侣蛋白(rictor)的表达。分别用raptor、rictor和雷帕霉素靶蛋白(mTOR)小干扰RNA(siRNA)转染嗜铬细胞瘤PC12细胞,以靶向mTORC1、mTORC2和mTORC1/2(mTORC1和mTORC2)。进行MTT法、凋亡分析、伤口愈合和Transwell实验。建立了携带PC12细胞异种移植瘤且用雷帕霉素或PP242给药的裸鼠肿瘤模型。在恶性PCC中,raptor的表达常为中度阳性,但rictor的表达常为强阳性。在体外,虽然抑制mTORC1能够抑制PC12细胞增殖,但抑制mTORC2更有效地抑制细胞增殖。抑制mTORC2或mTORC1/2更有效地阻止细胞迁移和侵袭,并促进细胞凋亡,而抑制mTORC1仅轻微阻止细胞迁移和侵袭,且不能促进凋亡。此外,我们发现靶向mTORC2会使mTOR下游激酶失调,但靶向mTORC1则不会。在体内,我们发现在肿瘤模型中,PP242在抑制肿瘤生长方面比雷帕霉素更有效。我们的数据表明,在治疗恶性PCC/PGL方面,靶向mTORC2可能比选择性靶向mTORC1更具优势。然而,需要更多的临床试验来证实我们的发现。

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