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6-Shogaol Inhibits Breast Cancer Cells and Stem Cell-Like Spheroids by Modulation of Notch Signaling Pathway and Induction of Autophagic Cell Death

机译:6-Shogaol通过调节Notch信号通路和诱导自噬细胞死亡来抑制乳腺癌细胞和类似干细胞的球体。

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摘要

Cancer stem cells (CSCs) pose a serious obstacle to cancer therapy as they can be responsible for poor prognosis and tumour relapse. In this study, we have investigated inhibitory activity of the ginger-derived compound 6-shogaol against breast cancer cells both in monolayer and in cancer-stem cell-like spheroid culture. The spheroids were generated from adherent breast cancer cells. 6-shogaol was effective in killing both breast cancer monolayer cells and spheroids at doses that were not toxic to noncancerous cells. The percentages of CD44+CD24-/low cells and the secondary sphere content were reduced drastically upon treatment with 6-shogaol confirming its action on CSCs. Treatment with 6-shogaol caused cytoplasmic vacuole formation and cleavage of microtubule associated protein Light Chain3 (LC3) in both monolayer and spheroid culture indicating that it induced autophagy. Kinetic analysis of the LC3 expression and a combination treatment with chloroquine revealed that the autophagic flux instigated cell death in 6-shogaol treated breast cancer cells in contrast to the autophagy inhibitor chloroquine. Furthermore, 6-shogaol-induced cell death got suppressed in the presence of chloroquine and a very low level of apoptosis was exhibited even after prolonged treatment of the compound, suggesting that autophagy is the major mode of cell death induced by 6-shogaol in breast cancer cells. 6-shogaol reduced the expression levels of Cleaved Notch1 and its target proteins Hes1 and Cyclin D1 in spheroids, and the reduction was further pronounced in the presence of a γ-secretase inhibitor. Secondary sphere formation in the presence of the inhibitor was also further reduced by 6-shogaol. Together, these results indicate that the inhibitory action of 6-shogaol on spheroid growth and sustainability is conferred through γ-secretase mediated down-regulation of Notch signaling. The efficacy of 6-shogaol in monolayer and cancer stem cell-like spheroids raise hope for its therapeutic benefit in breast cancer treatment.
机译:癌症干细胞(CSC)构成了癌症治疗的严重障碍,因为它们可能导致不良的预后和肿瘤复发。在这项研究中,我们研究了生姜化合物6-shogaol在单层和癌干细胞样球体培养物中对乳腺癌细胞的抑制活性。球体是由粘附的乳腺癌细胞产生的。 6-松果酚以对非癌细胞无毒的剂量有效杀死乳腺癌单层细胞和球体。 6-shogaol处理后,CD44 + CD24 - / low 细胞的百分比和次级球含量大大降低,证实了其对CSC的作用。用6-shogaol处理可导致细胞质液泡形成,并在单层和球形培养物中均裂解微管相关蛋白轻链3(LC3),表明它诱导了自噬。 LC3表达的动力学分析以及氯喹的联合治疗表明,与自噬抑制剂氯喹相反,自噬通量促进了6-松果酚处理的乳腺癌细胞的细胞死亡。此外,即使在长期使用该化合物后,在氯喹存在下6-shogaol诱导的细胞死亡也得到抑制,并且显示出非常低水平的凋亡,这表明自噬是6-shogaol诱导的乳腺癌细胞死亡的主要方式。癌细胞。 6-shogaol降低了球状体中Cleaved Notch1及其靶蛋白Hes1和Cyclin D1的表达水平,并且在存在γ-分泌酶抑制剂的情况下这种降低进一步明显。在存在抑制剂的情况下,次级球的形成也被6-松果酚进一步减少了。总之,这些结果表明6-松果酚对球体生长和可持续性的抑制作用是通过γ-分泌酶介导的Notch信号的下调而赋予的。 6-shogaol在单层和癌干细胞样球体中的功效为其在乳腺癌治疗中的治疗益处带来了希望。

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