靶向溶酶体:对抗癌症化疗抗药性的策略

IF 4.3 3区 材料科学 Q1 ENGINEERING, ELECTRICAL & ELECTRONIC
Ekta Shirbhate, Vaibhav Singh, Aditya Mishra, Varsha Jahoriya, Ravichandran Veerasamy, Amit K Tiwari, Harish Rajak
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引用次数: 0

摘要

化疗仍然是治疗多种癌症的主要方法。抗药性严重阻碍了癌症的治疗。溶酶体等酸性细胞器是细胞消化的主角。然而,由于溶酶体在癌症进展和抗药性方面的加速参与,溶酶体正日益受到人们的关注。例如,碱性弱化疗药物可渗透溶酶体膜,并以阳离子状态保留在溶酶体中,而溶酶体酶的细胞外释放会诱发癌症,溶酶体水解酶的细胞外逸会导致细胞凋亡等。由于溶酶体的药物螯合作用,药物在作用部位的可用性降低,这也增强了癌症的抗药性。本综述探讨溶酶体药物螯合机制及其如何影响癌症耐药性。利用溶酶体作为亚细胞靶点来对抗耐药性和逆转药物螯合是本文涉及的另一种克服耐药性的方法。本综述认为溶酶体药物螯合是导致化疗耐药性的原因之一。文章深入探讨了溶酶体螯合的具体方面,提供了针对溶酶体缺陷癌症的不同方法的细微见解、批判性评价或新颖诠释。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Targeting Lysosomes: A Strategy Against Chemoresistance in Cancer.

Chemotherapy is still the major method of treatment for many types of cancer. Curative cancer therapy is hampered significantly by medication resistance. Acidic organelles like lysosomes serve as protagonists in cellular digestion. Lysosomes, however, are gaining popularity due to their speeding involvement in cancer progression and resistance. For instance, weak chemotherapeutic drugs of basic nature permeate through the lysosomal membrane and are retained in lysosomes in their cationic state, while extracellular release of lysosomal enzymes induces cancer, cytosolic escape of lysosomal hydrolases causes apoptosis, and so on. Drug availability at the sites of action is decreased due to lysosomal drug sequestration, which also enhances cancer resistance. This review looks at lysosomal drug sequestration mechanisms and how they affect cancer treatment resistance. Using lysosomes as subcellular targets to combat drug resistance and reverse drug sequestration is another method for overcoming drug resistance that is covered in this article. The present review has identified lysosomal drug sequestration as one of the reasons behind chemoresistance. The article delves deeper into specific aspects of lysosomal sequestration, providing nuanced insights, critical evaluations, or novel interpretations of different approaches that target lysosomes to defect cancer.

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来源期刊
CiteScore
7.20
自引率
4.30%
发文量
567
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