دورية أكاديمية

MET fusions are targetable genomic variants in the treatment of advanced malignancies

التفاصيل البيبلوغرافية
العنوان: MET fusions are targetable genomic variants in the treatment of advanced malignancies
المؤلفون: Dantong Sun, Xiaoming Xing, Yongjie Wang, Helei Hou
المصدر: Cell Communication and Signaling, Vol 22, Iss 1, Pp 1-11 (2024)
بيانات النشر: BMC, 2024.
سنة النشر: 2024
المجموعة: LCC:Medicine
LCC:Cytology
مصطلحات موضوعية: Cancer, MET fusions, MET-TKIs, Targeted therapy, Medicine, Cytology, QH573-671
الوصف: Abstract Targeted therapy for malignancies has developed rapidly in recent years, benefiting patients harboring genetic mutations sensitive to relevant tyrosine kinase inhibitors (TKIs). With the development of targeted sequencing techniques, an increasing number of detectable genomic alterations in malignancies, including MET fusions, have been revealed. MET fusions, although rare among malignancies, might be functional driver genes that participate in activating downstream signaling pathways and promoting cell proliferation. Therefore, it is believed that MET fusions could be targetable genomic variants of MET, and inhibition of MET is considered an optionable therapeutic choice for patients harboring MET fusions. According to the summary presented in this review, we recommend MET-TKIs as suitable treatment agents for patients harboring primary MET fusions. For patients harboring acquired MET fusions after the development of resistance to TKIs targeting primary genomic alterations, such as sensitive EGFR mutations, treatment with a MET-TKI alone or in combination with TKIs targeting primary genomic alterations, such as EGFR-TKIs, is hypothesized to be a reasonable option for salvage treatment. In summary, MET fusions, despite their low incidence, should be taken into consideration when developing treatment strategies for cancer patients.
نوع الوثيقة: article
وصف الملف: electronic resource
اللغة: English
تدمد: 1478-811X
العلاقة: https://doaj.org/toc/1478-811XTest
DOI: 10.1186/s12964-023-01454-0
الوصول الحر: https://doaj.org/article/2961009cac3b441c8e633c54283c3b3fTest
رقم الانضمام: edsdoj.2961009cac3b441c8e633c54283c3b3f
قاعدة البيانات: Directory of Open Access Journals
الوصف
تدمد:1478811X
DOI:10.1186/s12964-023-01454-0