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重新审视 B-RAF 激酶在黑色素瘤治疗中的作用。

Revisiting the Role of B-RAF Kinase as a Therapeutic Target in Melanoma.

机构信息

Independent Radiopharmacy Unit, Faculty of Pharmacy, Medical University of Lublin, Lublin, PL, 20093, Poland.

Independent Radiopharmacy Unit, Faculty of Pharmacy, Medical University of Lublin, Lublin, PL-20093, Poland.

出版信息

Curr Med Chem. 2024;31(15):2003-2020. doi: 10.2174/0109298673258495231011065225.

DOI:10.2174/0109298673258495231011065225
PMID:37855341
Abstract

Malignant melanoma is the rarest but most aggressive and deadly skin cancer. Melanoma is the result of a malignant transformation of melanocytes, which leads to their uncontrolled proliferation. Mutations in the mitogen-activated protein kinase (MAPK) pathway, which are crucial for the control of cellular processes, such as apoptosis, division, growth, differentiation, and migration, are one of its most common causes. BRAF kinase, as one of the known targets of this pathway, has been known for many years as a prominent molecular target in melanoma therapy, and the following mini-review outlines the state-of-the-art knowledge regarding its structure, mutations and mechanisms.

摘要

恶性黑素瘤是最罕见但最具侵袭性和致命性的皮肤癌。黑素瘤是黑素细胞恶性转化的结果,导致其不受控制地增殖。丝裂原活化蛋白激酶(MAPK)途径中的突变是细胞过程(如细胞凋亡、分裂、生长、分化和迁移)控制的关键,这是其最常见的原因之一。BRAF 激酶作为该途径的已知靶点之一,多年来一直是黑色素瘤治疗中的一个重要分子靶点,以下简要综述概述了其结构、突变和机制的最新知识。

相似文献

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Revisiting the Role of B-RAF Kinase as a Therapeutic Target in Melanoma.重新审视 B-RAF 激酶在黑色素瘤治疗中的作用。
Curr Med Chem. 2024;31(15):2003-2020. doi: 10.2174/0109298673258495231011065225.
2
Mitogen-activated protein kinase dependency in BRAF/RAS wild-type melanoma: A rationale for combination inhibitors.丝裂原活化蛋白激酶依赖性在 BRAF/RAS 野生型黑色素瘤中:联合抑制剂的原理。
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The BRAF(V600E) inhibitor, PLX4032, increases type I collagen synthesis in melanoma cells.BRAF(V600E)抑制剂PLX4032可增加黑色素瘤细胞中I型胶原蛋白的合成。
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The mitogen-activated protein kinase pathway plays a critical role in regulating immunological properties of BRAF mutant cutaneous melanoma cells.丝裂原活化蛋白激酶途径在调节BRAF突变型皮肤黑色素瘤细胞的免疫特性中起关键作用。
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本文引用的文献

1
Triple Combination of Immune Checkpoint Inhibitors and BRAF/MEK Inhibitors in V600 Melanoma: Current Status and Future Perspectives.V600 黑色素瘤中免疫检查点抑制剂与 BRAF/MEK 抑制剂的三联组合:现状与未来展望
Cancers (Basel). 2022 Nov 8;14(22):5489. doi: 10.3390/cancers14225489.
2
Novel Biomarkers and Therapeutic Targets for Melanoma.新型黑色素瘤生物标志物与治疗靶点
Int J Mol Sci. 2022 Oct 1;23(19):11656. doi: 10.3390/ijms231911656.
3
Melanoma Management: From Epidemiology to Treatment and Latest Advances.黑色素瘤管理:从流行病学到治疗及最新进展
Cancers (Basel). 2022 Sep 24;14(19):4652. doi: 10.3390/cancers14194652.
4
BRAF Inhibitor Resistance in Melanoma: Mechanisms and Alternative Therapeutic Strategies.BRAF 抑制剂耐药性在黑色素瘤中的机制与治疗策略选择。
Curr Treat Options Oncol. 2022 Nov;23(11):1503-1521. doi: 10.1007/s11864-022-01006-7. Epub 2022 Oct 1.
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Terminal Phenoxy Group as a Privileged Moiety of the Drug Scaffold-A Short Review of Most Recent Studies 2013-2022.端酚氧基作为药物支架的优势部分——对 2013 年至 2022 年最新研究的综述。
Int J Mol Sci. 2022 Aug 9;23(16):8874. doi: 10.3390/ijms23168874.
6
New Potential Agents for Malignant Melanoma Treatment-Most Recent Studies 2020-2022.用于恶性黑素瘤治疗的新潜在药物-2020-2022 年最新研究。
Int J Mol Sci. 2022 May 29;23(11):6084. doi: 10.3390/ijms23116084.
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The future of targeted kinase inhibitors in melanoma.靶向激酶抑制剂在黑色素瘤中的未来。
Pharmacol Ther. 2022 Nov;239:108200. doi: 10.1016/j.pharmthera.2022.108200. Epub 2022 May 2.
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The Current State of Treatment and Future Directions in Cutaneous Malignant Melanoma.皮肤恶性黑色素瘤的治疗现状与未来方向
Biomedicines. 2022 Mar 31;10(4):822. doi: 10.3390/biomedicines10040822.
9
Circulating tumour DNA monitoring and early treatment for relapse: views from patients with early-stage melanoma.循环肿瘤 DNA 监测与早期复发治疗:早期黑色素瘤患者的观点。
Br J Cancer. 2022 Jun;126(10):1450-1456. doi: 10.1038/s41416-022-01766-x. Epub 2022 Mar 17.
10
Potential Anticancer Agents against Melanoma Cells Based on an As-Synthesized Thiosemicarbazide Derivative.基于合成的硫代卡巴肼衍生物的潜在抗癌剂对黑素瘤细胞的作用。
Biomolecules. 2022 Jan 18;12(2):151. doi: 10.3390/biom12020151.