Novel receptor tyrosine kinase-targeted strategies to overcome resistance in oral squamous cell carcinoma.

IF 3.6 3区 医学 Q2 PHARMACOLOGY & PHARMACY
Shahryar Irannejadrankouhi, Hassan Mivehchi, Aisan Eskandari-Yaghbastlo, Seyedeh Tabasom Nejati, Sahand Emrahoglu, Fatemeh Azarang, Abbas Nikroo, Mohsen Nabi-Afjadi
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引用次数: 0

Abstract

Treatment for oral squamous cell carcinoma (OSCC) has seen the rise of receptor tyrosine kinase inhibitors (RTKIs). However, their therapeutic effectiveness is severely limited by the emergence of resistance. Epidermal growth factor receptor (EGFR)-independent survival pathways, extracellular vesicle (EV)-mediated drug sequestration, lysosomal exocytosis, and metabolic reprogramming mediated by METTL1 (methyltransferase-like protein 1) are some of the molecular and cellular mechanisms that underlie RTKI resistance in OSCC. In this line, specific resistance methods are carefully studied, including the signaling processes involving SHP2, the different ways ErbB2 and AKT, and features related to tumor stemness. Additionally, the interaction between resistance and the tumor microenvironment (TME), namely via EVs and modified angiogenic signaling, is emphasized. Novel therapy approaches are put forth to address these issues. The effectiveness of treatment may be improved by combination treatments that include RTKIs with other medications, such as mTOR inhibitors, chemotherapy, radiation, and immunotherapies. Innovative nanotechnology-based strategies, such as exosome-based drug carriers and liposomal drug delivery systems, provide encouraging answers for overcoming resistance and enhancing precise targeting. Furthermore, phytochemicals and herbal remedies are investigated as supplementary approaches to enhance RTKI responses. Despite the potential of these approaches, obstacles, including resolving tumor heterogeneity, limiting off-target effects, and improving delivery methods, continue to be major obstacles to clinical use. To inform personalized medicine strategies, future studies should concentrate on finding predictive biomarkers and conducting thorough preclinical validation. By integrating emerging therapies and addressing these limitations, this work provides a comprehensive foundation for advancing the management of OSCC and improving patient outcomes.

新的受体酪氨酸激酶靶向策略克服口腔鳞状细胞癌的耐药。
口腔鳞状细胞癌(OSCC)的治疗已经看到受体酪氨酸激酶抑制剂(RTKIs)的上升。然而,由于耐药性的出现,它们的治疗效果受到严重限制。表皮生长因子受体(EGFR)独立的生存途径、细胞外囊泡(EV)介导的药物隔离、溶酶体胞吐和METTL1(甲基转移酶样蛋白1)介导的代谢重编程是OSCC中RTKI耐药的一些分子和细胞机制。在这条线中,我们仔细研究了具体的耐药方法,包括涉及SHP2的信号过程,ErbB2和AKT的不同途径,以及与肿瘤干性相关的特征。此外,还强调了耐药性与肿瘤微环境(TME)之间的相互作用,即通过ev和修饰的血管生成信号。新的治疗方法被提出来解决这些问题。通过将RTKIs与其他药物(如mTOR抑制剂、化疗、放疗和免疫疗法)联合治疗,可以提高治疗的有效性。基于创新纳米技术的策略,如基于外泌体的药物载体和脂质体药物递送系统,为克服耐药性和提高精确靶向性提供了令人鼓舞的答案。此外,还研究了植物化学物质和草药作为增强RTKI反应的补充方法。尽管这些方法具有潜力,但包括解决肿瘤异质性、限制脱靶效应和改进给药方法在内的障碍仍然是临床应用的主要障碍。为了为个性化医疗策略提供信息,未来的研究应集中于寻找预测性生物标志物并进行彻底的临床前验证。通过整合新兴疗法和解决这些局限性,这项工作为推进OSCC的管理和改善患者预后提供了全面的基础。
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来源期刊
Pharmacological Reports
Pharmacological Reports 医学-药学
CiteScore
8.40
自引率
0.00%
发文量
91
审稿时长
6 months
期刊介绍: Pharmacological Reports publishes articles concerning all aspects of pharmacology, dealing with the action of drugs at a cellular and molecular level, and papers on the relationship between molecular structure and biological activity as well as reports on compounds with well-defined chemical structures. Pharmacological Reports is an open forum to disseminate recent developments in: pharmacology, behavioural brain research, evidence-based complementary biochemical pharmacology, medicinal chemistry and biochemistry, drug discovery, neuro-psychopharmacology and biological psychiatry, neuroscience and neuropharmacology, cellular and molecular neuroscience, molecular biology, cell biology, toxicology. Studies of plant extracts are not suitable for Pharmacological Reports.
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