乳腺癌中肿瘤细胞诱导的血小板聚集:金属纳米颗粒的范围。

IF 9.7 1区 医学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY
Swathy Krishna Reghukumar, Iwona Inkielewicz-Stepniak
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引用次数: 0

摘要

乳腺癌是全球女性癌症相关死亡的主要原因。在促进乳腺癌转移的多种因素中,癌细胞血小板相互作用导致肿瘤细胞诱导的血小板聚集(TCIPA)的作用近年来引起了人们的广泛关注。我们最新的文献综述证实了金属纳米颗粒在乳腺癌研究和tcipa特异性乳腺癌转移中的意义。我们已经评估了在体外和体内的研究数据,以及在这个主题的范围内提出了在过去十年的临床调查。在癌症治疗中,基于纳米粒子的药物传递平台可以对抗日益增长的多药耐药、化疗引起的毒性和癌症进展的惊人速度。与化疗药物结合的金属纳米颗粒在实现靶向药物递送和肿瘤组织内所需药物浓度方面优于其游离药物,并且毒性作用最小。现有数据强调了金属纳米颗粒作为靶向与乳腺癌转移相关的血小板特异性相互作用(包括TCIPA)的有前途的工具的潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Tumour cell-induced platelet aggregation in breast cancer: Scope of metal nanoparticles
Breast cancer is a major cause of cancer-related mortality among the female population worldwide. Among the various factors promoting breast cancer metastasis, the role of cancer-cell platelet interactions leading to tumour cell-induced platelet aggregation (TCIPA) has garnered significant attention recently. Our state-of-the-art literature review verifies the implications of metal nanoparticles in breast cancer research and TCIPA-specific breast cancer metastasis. We have evaluated in vitro and in vivo research data as well as clinical investigations within the scope of this topic presented in the last ten years. Nanoparticle-based drug delivery platforms in cancer therapy can combat the growing concerns of multi-drug resistance, the alarming rates of chemotherapy-induced toxicities and cancer progression. Metal nanoparticles conjugated with chemotherapeutics can outperform their free drug counterparts in achieving targeted drug delivery and desired drug concentration inside the tumour tissue with minimal toxic effects. Existing data highlights the potential of metal nanoparticles as a promising tool for targeting the platelet-specific interactions associated with breast cancer metastasis including TCIPA.
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来源期刊
Biochimica et biophysica acta. Reviews on cancer
Biochimica et biophysica acta. Reviews on cancer 医学-生化与分子生物学
CiteScore
17.20
自引率
0.00%
发文量
138
审稿时长
33 days
期刊介绍: Biochimica et Biophysica Acta (BBA) - Reviews on Cancer encompasses the entirety of cancer biology and biochemistry, emphasizing oncogenes and tumor suppressor genes, growth-related cell cycle control signaling, carcinogenesis mechanisms, cell transformation, immunologic control mechanisms, genetics of human (mammalian) cancer, control of cell proliferation, genetic and molecular control of organismic development, rational anti-tumor drug design. It publishes mini-reviews and full reviews.
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