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靶向肝细胞癌中的表皮生长因子受体/磷脂酰肌醇-3激酶/蛋白激酶B/雷帕霉素靶蛋白信号通路

Targeting EGFR/PI3K/AKT/mTOR Signaling in Hepatocellular Carcinoma.

作者信息

Bang Jieun, Jun Mihyeon, Lee Soyun, Moon Hyuk, Ro Simon Weonsang

机构信息

Department of Genetics and Biotechnology, College of Life Sciences, Kyung Hee University, Yongin-si 17104, Republic of Korea.

出版信息

Pharmaceutics. 2023 Aug 14;15(8):2130. doi: 10.3390/pharmaceutics15082130.


DOI:10.3390/pharmaceutics15082130
PMID:37631344
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10458925/
Abstract

Hepatocellular carcinoma (HCC) poses a significant global health concern, with its incidence steadily increasing. The development of HCC is a multifaceted, multi-step process involving alterations in various signaling cascades. In recent years, significant progress has been made in understanding the molecular signaling pathways that play central roles in hepatocarcinogenesis. In particular, the EGFR/PI3K/AKT/mTOR signaling pathway in HCC has garnered renewed attention from both basic and clinical researchers. Preclinical studies in vitro and in vivo have shown the effectiveness of targeting the key components of this signaling pathway in human HCC cells. Thus, targeting these signaling pathways with small molecule inhibitors holds promise as a potential therapeutic option for patients with HCC. In this review, we explore recent advancements in understanding the role of the EGFR/PI3K/AKT/mTOR signaling pathway in HCC and assess the effectiveness of targeting this signaling cascade as a potential strategy for HCC therapy based on preclinical studies.

摘要

肝细胞癌(HCC)是一个重大的全球健康问题,其发病率在稳步上升。HCC的发展是一个多方面、多步骤的过程,涉及各种信号级联的改变。近年来,在理解在肝癌发生中起核心作用的分子信号通路方面取得了重大进展。特别是,HCC中的表皮生长因子受体/磷脂酰肌醇-3激酶/蛋白激酶B/雷帕霉素靶蛋白(EGFR/PI3K/AKT/mTOR)信号通路已重新引起基础和临床研究人员的关注。体外和体内的临床前研究表明,针对该信号通路的关键成分对人HCC细胞有效。因此,用小分子抑制剂靶向这些信号通路有望成为HCC患者的一种潜在治疗选择。在这篇综述中,我们探讨了在理解EGFR/PI3K/AKT/mTOR信号通路在HCC中的作用方面的最新进展,并根据临床前研究评估了靶向该信号级联作为HCC治疗潜在策略的有效性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/96ad/10458925/32ce456f8749/pharmaceutics-15-02130-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/96ad/10458925/32ce456f8749/pharmaceutics-15-02130-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/96ad/10458925/32ce456f8749/pharmaceutics-15-02130-g001.jpg

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Targeting EGFR/PI3K/AKT/mTOR Signaling in Hepatocellular Carcinoma.

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本文引用的文献

[1]
The Role of PI3K/AKT/mTOR Signaling in Hepatocellular Carcinoma Metabolism.

Int J Mol Sci. 2023-1-31

[2]
Co-administration of MDR1 and BCRP or EGFR/PI3K inhibitors overcomes lenvatinib resistance in hepatocellular carcinoma.

Front Oncol. 2022-9-8

[3]
DZW-310, a novel phosphoinositide 3-kinase inhibitor, attenuates the angiogenesis and growth of hepatocellular carcinoma cells via PI3K/AKT/mTOR axis.

Biochem Pharmacol. 2022-7

[4]
Target Therapy for Hepatocellular Carcinoma: Beyond Receptor Tyrosine Kinase Inhibitors and Immune Checkpoint Inhibitors.

Biology (Basel). 2022-4-12

[5]
Activated TAZ induces liver cancer in collaboration with EGFR/HER2 signaling pathways.

BMC Cancer. 2022-4-19

[6]
PI3K/Akt/mTOR Pathway and Its Role in Cancer Therapeutics: Are We Making Headway?

Front Oncol. 2022-3-24

[7]
Phase II Study of Copanlisib in Patients With Tumors With Mutations: Results From the NCI-MATCH ECOG-ACRIN Trial (EAY131) Subprotocol Z1F.

J Clin Oncol. 2022-5-10

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Liver Cancer. 2021-9-6

[9]
Targeting PI3K/Akt signal transduction for cancer therapy.

Signal Transduct Target Ther. 2021-12-16

[10]
Targeting the PI3K/Akt/mTOR Pathway in Hepatocellular Carcinoma.

Biomedicines. 2021-11-8

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