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Chloroquine diphosphate suppresses liver cancer via inducing apoptosis in Wistar rats using interventional therapy.磷酸氯喹通过介入治疗诱导Wistar大鼠凋亡来抑制肝癌。
Oncol Lett. 2021 Mar;21(3):233. doi: 10.3892/ol.2021.12494. Epub 2021 Jan 26.
2
Resistance of colon cancer to 5-fluorouracil may be overcome by combination with chloroquine, an in vivo study.体内研究显示,与氯喹联合应用可能克服结肠癌对 5-氟尿嘧啶的耐药性。
Anticancer Drugs. 2012 Aug;23(7):675-82. doi: 10.1097/CAD.0b013e328353f8c7.
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Chloroquine-based hybrid molecules as promising novel chemotherapeutic agents.基于氯喹的杂化分子作为有前景的新型化疗药物。
Eur J Pharmacol. 2015 Sep 5;762:472-86. doi: 10.1016/j.ejphar.2015.04.048. Epub 2015 May 8.
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Chloroquine upregulates TRAIL/TRAILR2 expression and potentiates doxorubicin anti-tumor activity in thioacetamide-induced hepatocellular carcinoma model.氯喹上调TRAIL/TRAILR2表达并增强阿霉素在硫代乙酰胺诱导的肝癌模型中的抗肿瘤活性。
Chem Biol Interact. 2018 Jan 5;279:84-94. doi: 10.1016/j.cbi.2017.11.009. Epub 2017 Nov 10.
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Abrogation of Autophagy by Chloroquine Alone or in Combination with mTOR Inhibitors Induces Apoptosis in Neuroendocrine Tumor Cells.单独使用氯喹或与mTOR抑制剂联合使用时对自噬的抑制会诱导神经内分泌肿瘤细胞凋亡。
Neuroendocrinology. 2016;103(6):724-37. doi: 10.1159/000442589. Epub 2015 Dec 1.
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Chloroquine exerts neuroprotection following traumatic brain injury via suppression of inflammation and neuronal autophagic death.氯喹通过抑制炎症和神经元自噬性死亡,在创伤性脑损伤后发挥神经保护作用。
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Chloroquine and hydroxychloroquine inhibit bladder cancer cell growth by targeting basal autophagy and enhancing apoptosis.氯喹和羟氯喹通过靶向基础自噬和增强细胞凋亡来抑制膀胱癌细胞生长。
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Chloroquine augments TRAIL-induced apoptosis and induces G2/M phase arrest in human pancreatic cancer cells.氯喹增强 TRAIL 诱导的人胰腺癌细胞凋亡并诱导 G2/M 期阻滞。
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Chloroquine inhibits hepatocellular carcinoma cell growth in vitro and in vivo.氯喹在体外和体内均能抑制肝癌细胞生长。
Oncol Rep. 2016 Jan;35(1):43-9. doi: 10.3892/or.2015.4380. Epub 2015 Nov 2.
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Honokiol exhibits enhanced antitumor effects with chloroquine by inducing cell death and inhibiting autophagy in human non-small cell lung cancer cells.厚朴酚与氯喹联合使用时,通过诱导人非小细胞肺癌细胞死亡和抑制自噬,表现出增强的抗肿瘤作用。
Oncol Rep. 2015 Sep;34(3):1289-300. doi: 10.3892/or.2015.4091. Epub 2015 Jun 29.

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The effect of chloroquine on cervical cancer via the PI3K/AKT/MDM2 pathway.氯喹通过PI3K/AKT/MDM2信号通路对宫颈癌的影响。
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Autophagy Inhibitor Chloroquine Downmodulates Hepatic Stellate Cell Activation and Liver Damage in Bile-Duct-Ligated Mice.自噬抑制剂氯喹下调胆管结扎小鼠肝星状细胞的激活和肝损伤。
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Combination of chloroquine diphosphate and salidroside induces human liver cell apoptosis via regulation of mitochondrial dysfunction and autophagy.磷酸氯喹和红景天苷通过调节线粒体功能障碍和自噬诱导人肝细胞凋亡。
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本文引用的文献

1
Effect of High vs Low Doses of Chloroquine Diphosphate as Adjunctive Therapy for Patients Hospitalized With Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) Infection: A Randomized Clinical Trial.高剂量与低剂量磷酸氯喹作为辅助治疗对住院的严重急性呼吸综合征冠状病毒 2(SARS-CoV-2)感染患者的影响:一项随机临床试验。
JAMA Netw Open. 2020 Apr 24;3(4):e208857. doi: 10.1001/jamanetworkopen.2020.8857.
2
Chloroquine and hydroxychloroquine in covid-19.氯喹和羟氯喹在2019冠状病毒病中的应用
BMJ. 2020 Apr 8;369:m1432. doi: 10.1136/bmj.m1432.
3
[Expert consensus on chloroquine phosphate for the treatment of novel coronavirus pneumonia].《磷酸氯喹治疗新型冠状病毒肺炎专家共识》
Zhonghua Jie He He Hu Xi Za Zhi. 2020 Mar 12;43(3):185-188. doi: 10.3760/cma.j.issn.1001-0939.2020.03.009.
4
Hepatic Stellate Cells in Liver Tumor.肝星状细胞在肝肿瘤中的作用。
Adv Exp Med Biol. 2020;1234:43-56. doi: 10.1007/978-3-030-37184-5_4.
5
Intratumoral heterogeneity and clonal evolution in liver cancer.肝癌中的肿瘤内异质性和克隆进化。
Nat Commun. 2020 Jan 15;11(1):291. doi: 10.1038/s41467-019-14050-z.
6
Cordycepin suppresses the migration and invasion of human liver cancer cells by downregulating the expression of CXCR4.虫草素通过下调 CXCR4 的表达抑制人肝癌细胞的迁移和侵袭。
Int J Mol Med. 2020 Jan;45(1):141-150. doi: 10.3892/ijmm.2019.4391. Epub 2019 Oct 31.
7
Joining the dots for better liver cancer treatment.为更好地治疗肝癌而连接各个要点。
Nat Rev Gastroenterol Hepatol. 2020 Feb;17(2):74-75. doi: 10.1038/s41575-019-0238-3.
8
Challenges in liver cancer and possible treatment approaches.肝癌的挑战与可能的治疗方法。
Biochim Biophys Acta Rev Cancer. 2020 Jan;1873(1):188314. doi: 10.1016/j.bbcan.2019.188314. Epub 2019 Nov 1.
9
Quantitative real time polymerase chain reaction (qRT-PCR) and RNAscope in situ hybridization (RNA-ISH) as effective tools to diagnose feline herpesvirus-1-associated dermatitis.定量实时聚合酶链反应(qRT-PCR)和RNAscope原位杂交(RNA-ISH)作为诊断猫疱疹病毒1型相关皮炎的有效工具。
Vet Dermatol. 2019 Dec;30(6):491-e147. doi: 10.1111/vde.12787. Epub 2019 Sep 5.
10
Modelling liver cancer initiation with organoids derived from directly reprogrammed human hepatocytes.利用直接重编程的人源肝细胞衍生类器官建立肝癌起始模型。
Nat Cell Biol. 2019 Aug;21(8):1015-1026. doi: 10.1038/s41556-019-0359-5. Epub 2019 Jul 22.

磷酸氯喹通过介入治疗诱导Wistar大鼠凋亡来抑制肝癌。

Chloroquine diphosphate suppresses liver cancer via inducing apoptosis in Wistar rats using interventional therapy.

作者信息

Hao Xiaoguang, Li Weijing

机构信息

Department of Radiology, The Fourth Hospital of Hebei Medicine University, Shijiazhuang, Hebei 050000, P.R. China.

Department of Anesthesiology, The Fourth Hospital of Hebei Medicine University, Shijiazhuang, Hebei 050000, P.R. China.

出版信息

Oncol Lett. 2021 Mar;21(3):233. doi: 10.3892/ol.2021.12494. Epub 2021 Jan 26.

DOI:10.3892/ol.2021.12494
PMID:33613722
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7856698/
Abstract

Liver cancer ranks as the second leading cause of cancer-associated mortality worldwide. To date, neither current ablation therapy nor chemotherapy are considered ideal in improving the outcome of liver cancer. Therefore, more effective therapies for treating this devastating disease are urgently required. Interventional therapy has been used for numerous years in the treatment of different types of cancer, and is characterized by the direct delivery of anticancer drugs into the tumor. It has been reported that antimalarial chloroquine diphosphate (CQ) exerts effective anticancer activity against several types of cancer. However, its effect on liver cancer remains unclear. Therefore, in the present study, 2D monolayer cell culture and 3D spheroid models, and a rat model, were utilized to investigate the effect of CQ on liver cancer. CQ demonstrated an effective anticancer effect on HepG2 cells and 3D liver spheroids. Furthermore, the drug significantly inhibited cell growth and viability in the 2D and 3D models. The CQ-based intervention treatment effectively attenuated tumor size and weight, increased food intake and consumption of drinking water, and improved body weight and survival rate of rats in the model. In addition, treatment with CQ potently increased the expression levels of the apoptosis-related genes. Taken together, the findings of the present study may provide a novel insight into the development of safe and effective treatments for liver cancer.

摘要

肝癌是全球癌症相关死亡的第二大主要原因。迄今为止,无论是目前的消融疗法还是化疗,在改善肝癌治疗效果方面都不被认为是理想的。因此,迫切需要更有效的疗法来治疗这种毁灭性疾病。介入治疗已在多种类型癌症的治疗中应用多年,其特点是将抗癌药物直接输送到肿瘤中。据报道,抗疟药磷酸氯喹(CQ)对几种类型的癌症具有有效的抗癌活性。然而,其对肝癌的作用仍不清楚。因此,在本研究中,利用二维单层细胞培养和三维球体模型以及大鼠模型来研究CQ对肝癌的影响。CQ对HepG2细胞和三维肝脏球体显示出有效的抗癌作用。此外,该药物在二维和三维模型中显著抑制细胞生长和活力。基于CQ的干预治疗有效减小了模型大鼠的肿瘤大小和重量,增加了食物摄入量和饮水量,并改善了体重和存活率。此外,CQ治疗有力地提高了凋亡相关基因的表达水平。综上所述,本研究结果可能为肝癌安全有效治疗方法的开发提供新的见解。