Yang Min Hee, Ha In Jin, Um Jae-Young, Ahn Kwang Seok
KHU-KIST Department of Converging Science and Technology, Kyung Hee University, Seoul 02447, Korea.
Department of Science in Korean Medicine, Kyung Hee University, 24 Kyungheedae-ro, Dongdaemun-gu, Seoul 02447, Korea.
Biomedicines. 2021 Mar 31;9(4):362. doi: 10.3390/biomedicines9040362.
Albendazole (ABZ) has been reported to display anti-tumoral actions against various maliganncies, but possible impact of ABZ on gastric cancer has not been deciphered. As aberrant phosphorylation of STAT3 and STAT5 proteins can regulate the growth and progression of gastric cancer, we postulated that ABZ may interrupt the activation of these oncogenic transcription factors. We found that ABZ exposure abrogated STAT3/5 activation, inhibited phosphorylation of Janus-activated kinases 1/2 and Src and enhanced the levels of SHP-1 protein. Silencing of SHP-1 gene by small interfering RNA (siRNA) reversed the ABZ-promoted attenuation of STAT3 as well as STAT5 activation and cellular apoptosis. In addition, these effects were noted to be driven by an augmented levels of reactive oxygen species caused by drug-induced GSH/GSSG imbalance. Thus, the data indicates that ABZ can modulate the activation of STAT3 and STAT5 by pleiotropic mechanisms in gastric cancer cells.
据报道,阿苯达唑(ABZ)对多种恶性肿瘤具有抗肿瘤作用,但ABZ对胃癌的潜在影响尚未明确。由于信号转导和转录激活因子3(STAT3)和信号转导和转录激活因子5(STAT5)蛋白的异常磷酸化可调节胃癌的生长和进展,我们推测ABZ可能会阻断这些致癌转录因子的激活。我们发现,ABZ处理可消除STAT3/5的激活,抑制Janus激活激酶1/2和Src的磷酸化,并提高SHP-1蛋白水平。通过小干扰RNA(siRNA)沉默SHP-1基因可逆转ABZ促进的STAT3和STAT5激活减弱以及细胞凋亡。此外,这些效应被认为是由药物诱导的谷胱甘肽(GSH)/氧化型谷胱甘肽(GSSG)失衡导致的活性氧水平升高所驱动。因此,数据表明ABZ可通过多种机制调节胃癌细胞中STAT3和STAT5的激活。