Andrographis paniculata methanol extract suppresses the phosphorylation of ETV6‑NTRK3.

IF 2.3 Q3 MEDICINE, RESEARCH & EXPERIMENTAL Biomedical reports Pub Date : 2023-07-01 DOI:10.3892/br.2023.1630
Hoang Thanh Chi, Vo Ngoc Tram, Nguyen Trung Quan, Bui Thi Kim Ly
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Abstract

ETS variant transcription factor 6 (ETV6)-neurotrophic receptor tyrosine kinase 3 (NTRK3) (EN) fusions are typically found in rare diseases, such as primary renal fibrosarcoma (only six cases have been reported), secretory carcinoma of the breast and salivary gland (1 case), and AML (4 cases). Few cases have been reported, and expression of the EN gene fusion requires additional clinical data and fundamental research to be supported. The aim of the present study was to determine the inhibitory effect of Andrographis paniculata methanol extract (MeAP) on EN-related cell lines, IMS-M2 and BaF3/EN, as well as evaluate the mechanism of action. Vero cells were used as control cells. Trypan blue staining and MTT were used to evaluate the inhibitory effect of MeAP on tested cells. Western blotting and immunoprecipitation were used to detect the activation of EN after MeAP treatment. The IC50 values of MeAP were found to be 12.38±0.57 µg/ml (IMS-M2) and 13.06±0.49 µg/ml (BaF3/EN). MeAP was observed to inhibit cell proliferation in a time, dose, and cell density-dependent manner. The IC50 value for MeAP in Vero cells was markedly higher, at 109.97±4.24 (µg/ml), indicating a much less sensitive effect. Furthermore, MeAP treatment inhibited EN phosphorylation and induced apoptosis in these cells. Collectively, the present study demonstrated that MeAP has an oncogenic effect on EN fusion-positive cell lines, in particular.

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穿心莲甲醇提取物抑制ETV6‑NTRK3的磷酸化。
ETS变异转录因子6 (ETV6)-神经营养受体酪氨酸激酶3 (NTRK3) (EN)融合通常见于罕见疾病,如原发性肾纤维肉瘤(仅报道了6例),乳腺和唾液腺分泌性癌(1例)和AML(4例)。报道的病例很少,EN基因融合的表达需要额外的临床数据和基础研究的支持。本研究旨在研究穿心莲甲醇提取物(MeAP)对EN相关细胞株、IMS-M2和BaF3/EN的抑制作用,并探讨其作用机制。Vero细胞作为对照细胞。台盼蓝染色和MTT法评价MeAP对被试细胞的抑制作用。采用Western blotting和免疫沉淀法检测MeAP处理后EN的活化情况。MeAP的IC50值分别为12.38±0.57µg/ml (IMS-M2)和13.06±0.49µg/ml (BaF3/EN)。MeAP对细胞增殖的抑制呈时间、剂量和细胞密度依赖性。MeAP在Vero细胞中的IC50值明显较高,为109.97±4.24(µg/ml),表明其敏感性低得多。此外,MeAP处理可抑制EN磷酸化并诱导这些细胞凋亡。总的来说,本研究表明MeAP尤其对EN融合阳性细胞系具有致癌作用。
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来源期刊
Biomedical reports
Biomedical reports MEDICINE, RESEARCH & EXPERIMENTAL-
CiteScore
4.10
自引率
0.00%
发文量
86
期刊介绍: Biomedical Reports is a monthly, peer-reviewed journal, dedicated to publishing research across all fields of biology and medicine, including pharmacology, pathology, gene therapy, genetics, microbiology, neurosciences, infectious diseases, molecular cardiology and molecular surgery. The journal provides a home for original research, case reports and review articles.
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