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通过降低多药耐药性和促进细胞凋亡,PI3K/mTOR 双重抑制剂 BEZ235 和纳米乳紫杉醇协同抑制耐药性结肠癌细胞生长。

Synergistic Inhibition of Drug-Resistant Colon Cancer Growth with PI3K/mTOR Dual Inhibitor BEZ235 and Nano-Emulsioned Paclitaxel via Reducing Multidrug Resistance and Promoting Apoptosis.

机构信息

Department of Pathology, The First Affiliated Hospital, School of Medicine, Shihezi University, Key Laboratory of Xinjiang Endemic and Ethnic Diseases of the Ministry of Education of China, Xinjiang, 832002, People's Republic of China.

Department of Oncology, Yongcheng People's Hospital, Henan, 476600, People's Republic of China.

出版信息

Int J Nanomedicine. 2021 Mar 15;16:2173-2186. doi: 10.2147/IJN.S290731. eCollection 2021.

Abstract

BACKGROUND

Colon cancer is a top lethal cancer in man and women worldwide and drug resistance is the major cause of cancer-related death. Combinational therapy and drug delivery with nanoparticles have been shown to effectively overcome drug resistance in many cancers. We previously reported that nanoemulsion (NE) loaded paclitaxel (PTX) and BEZ235 could synergistically inhibit colon cancer cell growth.

PURPOSE

To investigate whether NE loaded PTX and BEZ235 can overcome drug resistance and synergistically inhibit drug-resistant colon cancer cell growth in vitro and in vivo.

METHODS

The in vitro treatment effect on cell viability was assayed using CCK8 kit, cell morphological change was detected by β-tubulin immunofluorescence staining, drug resistance-related proteins were analyzed by Western blotting, and in vivo tumor growth test was performed in nude mice xeno-transplanted with 2 drug-resistant colon cancer cell lines HCT116-LOHP and HT29-DDP.

RESULTS

Both cell lines were sensitive to PTX but relatively insensitive to BEZ235. PTX combined with BEZ235 synergistically inhibited the proliferation of both cell lines. Nanoemulsion loaded PTX (NE-PTX) reduced the IC50 of PTX to approximately 2/5 of free PTX, indicating a high inhibitory efficacy of NE-PTX. When NE-PTX combined with a low concentration of BEZ235 (50 nM), the IC50 was decreased to approximately 2/3 of free PTX. Moreover, NE-PTX+BEZ235 treatment increased apoptosis, decreased Pgp and ABCC1 expression, and reduced tumor weights compared to the single drug treatment and the control group. These results suggest that nanoemulsion loaded PTX+BEZ235 can overcome drug resistance and improve the inhibitory effect on cancer cell proliferation and tumor growth.

CONCLUSION

Our study thus provides a possible new approach to treat colon cancer patients with drug resistance.

摘要

背景

结肠癌是全球男性和女性致死率最高的癌症之一,而耐药性是癌症相关死亡的主要原因。联合治疗和纳米颗粒载药已被证明能有效克服许多癌症的耐药性。我们之前曾报道过,载紫杉醇(PTX)和 BEZ235 的纳米乳(NE)能协同抑制结肠癌细胞生长。

目的

研究 NE 负载的 PTX 和 BEZ235 是否能克服耐药性并协同抑制体外和体内耐药性结肠癌细胞的生长。

方法

用 CCK8 试剂盒检测细胞活力的体外治疗效果,用β-微管蛋白免疫荧光染色检测细胞形态变化,用 Western blot 分析耐药相关蛋白,并用载有 2 种耐药结肠癌细胞系 HCT116-LOHP 和 HT29-DDP 的裸鼠异种移植进行体内肿瘤生长试验。

结果

这两种细胞系对 PTX 敏感,但对 BEZ235 相对不敏感。PTX 联合 BEZ235 协同抑制了这两种细胞系的增殖。载紫杉醇的纳米乳(NE-PTX)使 PTX 的 IC50 降低至游离 PTX 的约 2/5,表明 NE-PTX 具有较高的抑制效果。当 NE-PTX 与低浓度的 BEZ235(50 nM)联合使用时,IC50 降低至游离 PTX 的约 2/3。此外,与单药治疗和对照组相比,NE-PTX+BEZ235 治疗增加了细胞凋亡,降低了 Pgp 和 ABCC1 的表达,并减轻了肿瘤重量。这些结果表明,载紫杉醇的纳米乳+BEZ235 能克服耐药性,提高对癌细胞增殖和肿瘤生长的抑制作用。

结论

因此,我们的研究为治疗耐药性结肠癌患者提供了一种新的可能方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/36f9/7979685/1b1807f900ff/IJN-16-2173-g0001.jpg

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