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癌症干细胞及其龛内的经典和非经典 WNT 信号通路:细胞异质性、组学重编程、靶向治疗和肿瘤可塑性(综述)。

Canonical and non-canonical WNT signaling in cancer stem cells and their niches: Cellular heterogeneity, omics reprogramming, targeted therapy and tumor plasticity (Review).

机构信息

Department of Omics Network, National Cancer Center, Tokyo 104-0045, Japan.

出版信息

Int J Oncol. 2017 Nov;51(5):1357-1369. doi: 10.3892/ijo.2017.4129. Epub 2017 Sep 19.

Abstract

Cancer stem cells (CSCs), which have the potential for self-renewal, differentiation and de-differentiation, undergo epigenetic, epithelial-mesenchymal, immunological and metabolic reprogramming to adapt to the tumor microenvironment and survive host defense or therapeutic insults. Intra-tumor heterogeneity and cancer-cell plasticity give rise to therapeutic resistance and recurrence through clonal replacement and reactivation of dormant CSCs, respectively. WNT signaling cascades cross-talk with the FGF, Notch, Hedgehog and TGFβ/BMP signaling cascades and regulate expression of functional CSC markers, such as CD44, CD133 (PROM1), EPCAM and LGR5 (GPR49). Aberrant canonical and non-canonical WNT signaling in human malignancies, including breast, colorectal, gastric, lung, ovary, pancreatic, prostate and uterine cancers, leukemia and melanoma, are involved in CSC survival, bulk-tumor expansion and invasion/metastasis. WNT signaling-targeted therapeutics, such as anti-FZD1/2/5/7/8 monoclonal antibody (mAb) (vantictumab), anti-LGR5 antibody-drug conjugate (ADC) (mAb-mc-vc-PAB-MMAE), anti-PTK7 ADC (PF-06647020), anti-ROR1 mAb (cirmtuzumab), anti-RSPO3 mAb (rosmantuzumab), small-molecule porcupine inhibitors (ETC-159, WNT-C59 and WNT974), tankyrase inhibitors (AZ1366, G007-LK, NVP-TNKS656 and XAV939) and β-catenin inhibitors (BC2059, CWP232228, ICG-001 and PRI-724), are in clinical trials or preclinical studies for the treatment of patients with WNT-driven cancers. WNT signaling-targeted therapeutics are applicable for combination therapy with BCR-ABL, EGFR, FLT3, KIT or RET inhibitors to treat a subset of tyrosine kinase-driven cancers because WNT and tyrosine kinase signaling cascades converge to β-catenin for the maintenance and expansion of CSCs. WNT signaling-targeted therapeutics might also be applicable for combination therapy with immune checkpoint blockers, such as atezolizumab, avelumab, durvalumab, ipilimumab, nivolumab and pembrolizumab, to treat cancers with immune evasion, although the context-dependent effects of WNT signaling on immunity should be carefully assessed. Omics monitoring, such as genome sequencing and transcriptome tests, immunohistochemical analyses on PD-L1 (CD274), PD-1 (PDCD1), ROR1 and nuclear β-catenin and organoid-based drug screening, is necessary to determine the appropriate WNT signaling-targeted therapeutics for cancer patients.

摘要

癌症干细胞(CSCs)具有自我更新、分化和去分化的潜能,通过表观遗传、上皮-间充质、免疫和代谢重编程来适应肿瘤微环境,并在宿主防御或治疗性攻击中存活下来。肿瘤内异质性和癌细胞可塑性通过克隆替代和休眠 CSCs 的重新激活,分别导致治疗抵抗和复发。WNT 信号级联与 FGF、Notch、Hedgehog 和 TGFβ/BMP 信号级联相互作用,并调节功能性 CSC 标志物的表达,如 CD44、CD133(PROM1)、EPCAM 和 LGR5(GPR49)。人类恶性肿瘤中异常的经典和非经典 WNT 信号,包括乳腺癌、结直肠癌、胃癌、肺癌、卵巢癌、胰腺癌、前列腺癌和子宫癌、白血病和黑色素瘤,参与 CSC 的存活、肿瘤的大量扩增以及侵袭/转移。WNT 信号靶向治疗药物,如抗 FZD1/2/5/7/8 单克隆抗体(mAb)(vantictumab)、抗 LGR5 抗体-药物偶联物(ADC)(mAb-mc-vc-PAB-MMAE)、抗 PTK7 ADC(PF-06647020)、抗 ROR1 mAb(cirmtuzumab)、抗 RSPO3 mAb(rosmantuzumab)、小分子刺猬抑制剂(ETC-159、WNT-C59 和 WNT974)、 Tankyrase 抑制剂(AZ1366、G007-LK、NVP-TNKS656 和 XAV939)和 β-连环蛋白抑制剂(BC2059、CWP232228、ICG-001 和 PRI-724),正在临床试验或临床前研究中用于治疗 WNT 驱动的癌症患者。WNT 信号靶向治疗药物可与 BCR-ABL、EGFR、FLT3、KIT 或 RET 抑制剂联合治疗,以治疗一部分酪氨酸激酶驱动的癌症,因为 WNT 和酪氨酸激酶信号通路会汇集到β-连环蛋白上,以维持和扩增 CSCs。WNT 信号靶向治疗药物也可与免疫检查点抑制剂联合治疗,如 atezolizumab、avelumab、durvalumab、ipilimumab、nivolumab 和 pembrolizumab,以治疗具有免疫逃逸的癌症,尽管应谨慎评估 WNT 信号对免疫的上下文相关影响。需要进行组学监测,如基因组测序和转录组测试、PD-L1(CD274)、PD-1(PDCD1)、ROR1 和核β-连环蛋白的免疫组织化学分析以及基于类器官的药物筛选,以确定适合癌症患者的 WNT 信号靶向治疗药物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2087/5642388/885306186fe1/IJO-51-05-1357-g00.jpg

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