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CCT196969 有效抑制黑色素瘤脑转移细胞的生长和存活。

CCT196969 effectively inhibits growth and survival of melanoma brain metastasis cells.

机构信息

Department of Biomedicine, University of Bergen, Bergen, Norway.

Faculty of Health and Social Sciences, Western Norway University of Applied Sciences, Bergen, Norway.

出版信息

PLoS One. 2022 Sep 9;17(9):e0273711. doi: 10.1371/journal.pone.0273711. eCollection 2022.

Abstract

Melanomas frequently metastasize to the brain. Despite recent progress in the treatment of melanoma brain metastasis, therapy resistance and relapse of disease remain unsolved challenges. CCT196969 is a SRC family kinase (SFK) and Raf proto-oncogene, serine/threonine kinase (RAF) inhibitor with documented effects in primary melanoma cell lines in vitro and in vivo. Using in vitro cell line assays, we studied the effects of CCT196969 in multiple melanoma brain metastasis cell lines. The drug effectively inhibited proliferation, migration, and survival in all examined cell lines, with viability IC50 doses in the range of 0.18-2.6 μM. Western blot analysis showed decreased expression of p-ERK, p-MEK, p-STAT3 and STAT3 upon CCT196969 treatment. Furthermore, CCT196969 inhibited viability in two B-Raf Proto-Oncogene (BRAF) inhibitor resistant metastatic melanoma cell lines. Further in vivo studies should be performed to determine the treatment potential of CCT196969 in patients with treatment-naïve and resistant melanoma brain metastasis.

摘要

黑色素瘤经常转移到大脑。尽管最近在治疗黑色素瘤脑转移方面取得了进展,但治疗耐药性和疾病复发仍然是未解决的挑战。CCT196969 是一种 SRC 家族激酶 (SFK) 和 Raf 原癌基因丝氨酸/苏氨酸激酶 (RAF) 抑制剂,在体外和体内的原发性黑色素瘤细胞系中均有记载。通过体外细胞系测定,我们研究了 CCT196969 在多种黑色素瘤脑转移细胞系中的作用。该药物有效地抑制了所有检查的细胞系中的增殖、迁移和存活,其存活率 IC50 剂量在 0.18-2.6 μM 范围内。Western blot 分析显示,CCT196969 处理后 p-ERK、p-MEK、p-STAT3 和 STAT3 的表达减少。此外,CCT196969 抑制了两种 BRAF 抑制剂耐药性转移性黑色素瘤细胞系的活力。应进一步进行体内研究,以确定 CCT196969 在未经治疗和耐药性黑色素瘤脑转移患者中的治疗潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b702/9462752/c67d37d7a976/pone.0273711.g001.jpg

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