Temozolomide alleviates breast carcinoma via the inhibition of EGFR/ERK/ MMP-1 pathway with induction of apoptotic events

Weijun Zhu, Fengjun Zhang, Maoyun Wang, Shuai Meng, Fang Ren
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Abstract

Purpose: To evaluate the chemotherapeutic activity of temozolomide counter to mammary carcinoma. Methods: In-vitro anticancer activity has been conducted on MCF7 cells, and mammary carcinoma has been induced in Wistar rats by introduction of 7, 12-Dimethylbenz(a)anthracene (DMBA), which was sustained for 24 weeks. Histopathology, immunohistochemistry, cell proliferation study and apoptosis assay via TUNEL method was conducted to evaluate an antineoplastic activity of temozolomide in rat breast tissue. Results: IC50 value of temozolomide in MCF7 cell has been obtained as 103 μM, which demonstrated an initiation of apoptosis. The temozolomide treatment facilitated cell cycle arrest in G2/M and S phase dose dependently. The treatment with temozolomide suggested decrease of the hyperplastic abrasions and renovation of the typical histological features of mammary tissue. Moreover, temozolomide therapy caused the downregulation of epidermal growth factor receptor, extracellular signal-regulated kinase, and metalloproteinase-1 expression and upstream of p53 and caspase-3 proliferation to indicate an initiation of apoptotic events. Conclusions: The occurrence of mammary carcinoma has been significantly decreased by activation of apoptotic pathway and abrogation of cellular propagation that allowable for developing a suitable mechanistic pathway of temozolomide in order to facilitate chemotherapeutic approach.
替莫唑胺通过抑制表皮生长因子受体/ERK/MMP-1通路和诱导凋亡事件缓解乳腺癌病情
目的:评估替莫唑胺对乳腺癌的化疗活性。方法对 MCF7 细胞进行体外抗癌实验,并通过引入 7,12-二甲基苯(a)蒽(DMBA)诱导 Wistar 大鼠患乳腺癌,持续 24 周。通过组织病理学、免疫组化、细胞增殖研究和 TUNEL 法细胞凋亡检测,评估替莫唑胺在大鼠乳腺组织中的抗肿瘤活性。结果在 MCF7 细胞中,替莫唑胺的 IC50 值为 103 μM,这表明细胞开始凋亡。替莫唑胺治疗可促进细胞周期停滞在 G2/M 期和 S 期,且与剂量有关。替莫唑胺治疗可减少增生性擦伤,并恢复乳腺组织的典型组织学特征。此外,替莫唑胺治疗导致表皮生长因子受体、细胞外信号调节激酶和金属蛋白酶-1表达下调,p53和caspase-3增殖上行,表明凋亡事件开始发生。结论通过激活细胞凋亡途径和抑制细胞繁殖,乳腺癌的发病率明显降低,从而可以开发出适合替莫唑胺的机理途径,以促进化疗方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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