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氯喹通过抑制自噬作用防止三阴性乳腺癌模型对 PI3K/AKT 抑制剂产生耐药性,并增强其与紫杉醇联合的抗肿瘤作用。

Inhibition of autophagy by chloroquine prevents resistance to PI3K/AKT inhibitors and potentiates their antitumor effect in combination with paclitaxel in triple negative breast cancer models.

机构信息

Department of Breast and Thoracic Oncology, Division of Breast Medical Oncology, Istituto Nazionale Tumori IRCCS "Fondazione G. Pascale", 80131, Naples, Italy.

Experimental Pharmacology Unit, Laboratories of Naples and Mercogliano (AV), Istituto Nazionale Tumori IRCCS "Fondazione G. Pascale", 80131, Naples, Italy.

出版信息

J Transl Med. 2022 Jun 27;20(1):290. doi: 10.1186/s12967-022-03462-z.

Abstract

BACKGROUND

Triple negative breast cancer (TNBC) is an aggressive disease characterized by high risk of relapse and development of resistance to different chemotherapy agents. Several targeted therapies have been investigated in TNBC with modest results in clinical trials. Among these, PI3K/AKT inhibitors have been evaluated in addition to standard therapies, yielding conflicting results and making attempts on elucidating inherent mechanisms of resistance of great interest. Increasing evidences suggest that PI3K/AKT inhibitors can induce autophagy in different cancers. Autophagy represents a supposed mechanism of drug-resistance in aggressive tumors, like TNBC. We, therefore, investigated if two PI3K/AKT inhibitors, ipatasertib and taselisib, could induce autophagy in breast cancer models, and whether chloroquine (CQ), a well known autophagy inhibitor, could potentiate ipatasertib and taselisib anti-cancer effect in combination with conventional chemotherapy.

METHODS

The induction of autophagy after ipatasertib and taselisib treatment was evaluated in MDAMB231, MDAM468, MCF7, SKBR3 and MDAB361 breast cancer cell lines by assaying LC3-I conversion to LC3-II through immunoblotting and immunofluorescence. Other autophagy-markers as p62/SQSTM1 and ATG5 were evaluated by immunoblotting. Synergistic antiproliferative effect of double and triple combinations of ipatasertib/taselisib plus CQ and/or paclitaxel were evaluated by SRB assay and clonogenic assay. Anti-apoptotic effect of double combination of ipatasertib/taselisib plus CQ was evaluated by increased cleaved-PARP by immunoblot and by Annexin V- flow cytometric analysis. In vivo experiments were performed on xenograft model of MDAMB231 in NOD/SCID mice.

RESULTS

Our results suggested that ipatasertib and taselisib induce increased autophagy signaling in different breast cancer models. This effect was particularly evident in PI3K/AKT resistant TNBC cells, where the inhibition of autophagy by CQ potentiates the therapeutic effect of PI3K/AKT inhibitors in vitro and in vivo TNBC models, synergizing with taxane-based chemotherapy.

CONCLUSION

These data suggest that inhibition of authophagy with CQ could overcome mechanism of drug resistance to PI3K/AKT inhibitors plus paclitaxel in TNBC making the evaluation of such combinations in clinical trials warranted.

摘要

背景

三阴性乳腺癌(TNBC)是一种侵袭性疾病,其特征是复发风险高,对不同化疗药物的耐药性发展。已经有几种针对 TNBC 的靶向治疗方法在临床试验中进行了评估,但结果仅为适度。在这些治疗方法中,除了标准疗法外,还评估了 PI3K/AKT 抑制剂,但结果相互矛盾,阐明其固有耐药机制的尝试引起了极大的兴趣。越来越多的证据表明,PI3K/AKT 抑制剂可在不同癌症中诱导自噬。自噬是 TNBC 等侵袭性肿瘤中一种假定的耐药机制。因此,我们研究了两种 PI3K/AKT 抑制剂 ipatasertib 和 taselisib 是否可在乳腺癌模型中诱导自噬,以及氯喹(CQ)作为一种众所周知的自噬抑制剂,是否可以增强 ipatasertib 和 taselisib 与常规化疗联合的抗癌作用。

方法

通过免疫印迹和免疫荧光法检测 LC3-I 向 LC3-II 的转化,评估 ipatasertib 和 taselisib 处理后自噬的诱导。通过免疫印迹评估其他自噬标志物如 p62/SQSTM1 和 ATG5。通过 SRB 测定和集落形成测定评估 ipatasertib/taselisib 加 CQ 和/或紫杉醇的双重和三重组合的协同抗增殖作用。通过免疫印迹和 Annexin V-流式细胞术分析检测 ipatasertib/taselisib 加 CQ 的双重组合的抗凋亡作用。在 NOD/SCID 小鼠的 MDAMB231 异种移植模型中进行了体内实验。

结果

我们的结果表明,ipatasertib 和 taselisib 在不同的乳腺癌模型中诱导自噬信号增加。这种作用在 PI3K/AKT 耐药性 TNBC 细胞中尤为明显,其中 CQ 抑制自噬可增强 PI3K/AKT 抑制剂在体外和体内 TNBC 模型中的治疗效果,与紫杉醇为基础的化疗协同作用。

结论

这些数据表明,用 CQ 抑制自噬可能会克服 TNBC 对 PI3K/AKT 抑制剂加紫杉醇的耐药机制,因此值得在临床试验中评估此类组合。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/af8f/9235112/e57dc1e398bd/12967_2022_3462_Fig1_HTML.jpg

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