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除BRAF突变黑色素瘤外的黑色素瘤靶向治疗:潜在的可药物化突变和新的治疗方法。

Melanoma Targeted Therapies beyond -Mutant Melanoma: Potential Druggable Mutations and Novel Treatment Approaches.

作者信息

Khaddour Karam, Maahs Lucas, Avila-Rodriguez Ana Maria, Maamar Yazan, Samaan Sami, Ansstas George

机构信息

Division of Medical Oncology, Department of Medicine, Washington University in Saint Louis, Saint Louis, MO 63130, USA.

Division of Hematology and Oncology, Department of Medicine, University of Illinois at Chicago, Chicago, IL 60612, USA.

出版信息

Cancers (Basel). 2021 Nov 22;13(22):5847. doi: 10.3390/cancers13225847.

DOI:10.3390/cancers13225847
PMID:34831002
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8616477/
Abstract

Melanomas exhibit the highest rate of somatic mutations among all different types of cancers (with the exception of BCC and SCC). The accumulation of a multimode of mutations in the driver oncogenes are responsible for the proliferative, invasive, and aggressive nature of melanomas. High-resolution and high-throughput technology has led to the identification of distinct mutational signatures and their downstream alterations in several key pathways that contribute to melanomagenesis. This has enabled the development of individualized treatments by targeting specific molecular alterations that are vital for cancer cell survival, which has resulted in improved outcomes in several cancers, including melanomas. To date, and inhibitors remain the only approved targeted therapy with a high level of evidence in mutant melanomas. The lack of approved precision drugs in melanomas, relative to other cancers, despite harboring one of the highest rates of somatic mutations, advocates for further research to unveil effective therapeutics. In this review, we will discuss potential druggable mutations and the ongoing research of novel individualized treatment approaches targeting non- mutations in melanomas.

摘要

黑色素瘤在所有不同类型的癌症中(基底细胞癌和鳞状细胞癌除外)表现出最高的体细胞突变率。驱动癌基因中多种突变的积累导致了黑色素瘤的增殖、侵袭和侵袭性。高分辨率和高通量技术已导致在几种有助于黑色素瘤发生的关键途径中识别出独特的突变特征及其下游改变。这使得通过靶向对癌细胞存活至关重要的特定分子改变来开发个体化治疗成为可能,这已在包括黑色素瘤在内的几种癌症中带来了更好的治疗效果。迄今为止, 和 抑制剂仍然是在 突变黑色素瘤中唯一有高度证据支持的获批靶向治疗药物。尽管黑色素瘤的体细胞突变率是最高的之一,但相对于其他癌症,其缺乏获批的精准药物,这促使人们进一步开展研究以揭示有效的治疗方法。在本综述中,我们将讨论潜在的可药物化突变以及针对黑色素瘤中非 突变的新型个体化治疗方法的 ongoing 研究。 (注:原文中“To date, and inhibitors remain...”和“ongoing research”处表述似乎不完整,可能影响对完整意思的理解,但按要求逐字翻译了。)

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7385/8616477/3acceb51cc43/cancers-13-05847-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7385/8616477/4a814cf25fde/cancers-13-05847-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7385/8616477/a306be8f9e3e/cancers-13-05847-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7385/8616477/9e7910ecbbd7/cancers-13-05847-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7385/8616477/fd8e1e029e48/cancers-13-05847-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7385/8616477/3acceb51cc43/cancers-13-05847-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7385/8616477/4a814cf25fde/cancers-13-05847-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7385/8616477/a306be8f9e3e/cancers-13-05847-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7385/8616477/9e7910ecbbd7/cancers-13-05847-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7385/8616477/fd8e1e029e48/cancers-13-05847-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7385/8616477/3acceb51cc43/cancers-13-05847-g005.jpg

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